RELATED APPLICATIONS 0001 This application is a continuation of U.S. patent application Ser. No. 09/268,135, filed Mar. 12, 1999 (Lyon & Lyon Docket No. 240/223), which relates to U.S. patent application Ser. No. 08/949,160, filed Oct. 10, 1997 and International patent application No. PCT/US97/18779, filed Oct. 10, 1997, (Lyon & Lyon Docket Nos. 226/285 US and PCT, respectively), both of which are related to U.S. patent application Serial No. 60/028,676, filed Oct. 18, 1996, (Lyon & Lyon Docket No. 222/086 US), all three of which are entitled IL-12 GENE EXPRESSION AND DELIVERY SYSTEMS AND USES (by Nordstrom et al.). 0002 This application is also related to U.S. patent application Ser. No. 08/798,974, filed Feb. 11, 1997, (Lyon & Lyon Docket No. 224/084 US) and International patent application No. PCT/US95/17038, filed Dec. 28, 1995, (Lyon & Lyon Docket No. 210/190 PCT), both of which are related to U.S. patent application Ser. No. 08/372,213, filed Jan. 13, 1995, (Lyon & Lyon Docket No. 210/190 US), all three of which are entitled FORMULATED NUCLEIC ACID COMPOSITIONS AND METHODS OF ADMINISTERING THE SAME FOR GENE THERAPY (by Mumper Rolland). 0003 Each of the above-mentioned applications are incorporated herein by reference in their entirety, including any drawings.

FIELD OF THE INVENTION 0004 The present invention relates to gene delivery and gene therapy, and provides novel nucleic acid constructs for expression of interferon alpha in a mammal, formulations for delivery that incorporate a nucleic acid construct for expression, and methods for preparing and using such constructs and formulations. In particular, this invention relates to plasmid constructs for delivery of therapeutic interferon alpha encoding nucleic acids to cells in order to modulate tumor activity, methods of using those constructs (including combination therapy with other agents, such as cytokines, preferably IL-12), as well as methods for preparing such constructs.

BACKGROUND OF THE INVENTION 0005 The following discussion of the background of the invention is merely provided to aid the reader in understanding the invention and is not admitted to describe or constitute prior art to the present invention. 0006 Plasmids are an important element in genetic engineering and gene therapy. Plasmids are usually circular DNA molecules that can be introduced into bacterial cells by transformation which replicate autonomously in the cell. Plasmids typically allow for the amplification of cloned DNA. Some plasmids are present in 20 to 50 copies during cell growth, and after the arrest of protein synthesis, as many as 1000 copies per cell of a plasmid can be generated. Suzuki et al., Genetic Analysis, p. 404, 1989. 0007 Current non-viral approaches to human gene therapy require that a potential therapeutic gene be cloned into plasmids. Large quantities of a bacterial host harboring the plasmid may be fermented and the plasmid DNA may be purified for subsequent use. Current human clinical trials using plasmids utilize this approach. Recombinant DNA Advisory Committee Data Management Report, December, 1994, Human Gene Therapy 6:535-548. Studies normally focus on the therapeutic gene and the elements that control its expression in the patient when designing and constructing gene therapy plasmids. Generally, therapeutic genes and regulatory elements are simply inserted into existing cloning vectors that are convenient and readily available. 0008 Plasmid design and construction utilizes several key factors. First, plasmid replication origins determine plasmid copy number, which affects production yields. Plasmids that replicate to higher copy number can increase plasmid yield from a given volume of culture, but excessive copy number can be deleterious to the bacteria and lead to undesirable effects (Fitzwater, et al., Embo J. 7:3289-3297 (1988); Uhlin, et al., Mol. Gen. Genet. 165:167-179 (1979)). Artificially constructed plasmids are sometimes unstably maintained, leading to accumulation of plasmid-free cells and reduced production yields. 0009 To overcome this problem of plasmid-free cells, genes that code for antibiotic resistance phenotype are included on the plasmid and antibiotics are added to kill or inhibit plasmid-free cells. Most general purpose cloning vectors contain ampicillin resistance (-lactamase, or bla) genes. Use of ampicillin can be problematic because of the potential for residual antibiotic in the purified DNA, which can cause an allergic reaction in a treated patient. In addition, -lactam antibiotics are clinically important for disease treatment. When plasmids containing antibiotic resistance genes are used, the potential exists for the transfer of antibiotic resistance genes to a potential pathogen. 0010 Other studies have used the neo gene which is derived from the bacterial transposon Tn5. The neo gene encodes resistance to kanamycin and neomycin (Smith, Vaccine 12:1515-1519 (1994)). This gene has been used in a number of gene therapy studies, including several human clinical trials (Recombinant DNA Advisory Committee Data Management Report, December, 1994, Human Gene Therapy 6:535-548). Due to the mechanism by which resistance is imparted, residual antibiotic and transmission of the gene to potential pathogens may be less of a problem than for -lactams. 0011 In addition to elements that affect the behavior of the plasmid within the host bacteria, such as E. coli, plasmid vectors have also been shown to affect transfection and expression in eukaryotic cells. Certain plasmid sequences have been shown to reduce expression of eukaryotic genes in eukaryotic cells when carried in cis (Peterson, et al., Mol. Cell. Biol. 7:1563-1567 (1987); Yoder et al., Mol. Cell. Biol. 3:956-959 (1983); Lusky et al., Nature 293:79-81 (1981); and Leite, et al., Gene 82:351-356 (1989)). Plasmid sequences also have been shown to fortuitously contain binding sites for transcriptional control proteins (Ghersa, et al., Gene 151:331-332 (1994); Tully et al., Biochem. Biophys. Res. Comm. 144:1-10 (1987); and Kushner, et al., Mol. Endocrinol. 8:405-407 (1994)). This can cause inappropriate levels of gene expression in treated patients. 0012 Interferon alpha is a gene product that has been proposed for use, either alone or in combination with other agents, in different delivery systems for the treatment of certain diseases, including particular cancers. International patent publication WO/97/00085, published Jan. 3, 1997, proposes ex vivo transfection of tumor cells with interferon alpha and another immomodulatory molecule, such as IL-12. None of the previously proposed treatments have proven entirely satisfactory, due in part to the high cost and technical difficulty involved in ex vivo approaches. Thus there still remains a need in the art for improved plasmids encoding interferon alpha as well as improved treatment protocols and technologies.

SUMMARY 0013 The present invention relates to gene delivery and gene therapy, and provides novel nucleic acid constructs for expression of interferon alpha in a mammal, formulations for delivery that incorporate a nucleic acid construct for expression, and methods for preparing and using such constructs and formulations. In particular, this invention relates to plasmid constructs for delivery of therapeutic interferon alpha encoding nucleic acids to cells in order to modulate tumor activity, methods of using those constructs (including combination therapy with other agents, such as cytokines, preferably IL-12), as well as methods for preparing such constructs. The pharmaceutical acceptable, cost effective and highly efficient delivery system presented herein represents an unanticipated improvement over the art. 0014 Thus, in a first aspect, the invention features a plasmid that contains a CMV promoter and optionally a synthetic 5 intron transcriptionally linked with an interferon alpha coding sequence, and a 3-untranslated region (UTR). Preferably the 3 UTR is a 3 growth hormone UTR. 0015 As used herein, the term plasmid refers to a construct made up of genetic material (i.e., nucleic acids). It includes genetic elements arranged such that an inserted coding sequence can be transcribed in eukaryotic cells. Also, while the plasmid may include a sequence from a viral nucleic acid, such viral sequence does not cause the incorporation of the plasmid into a viral particle, and the plasmid is therefore a non-viral vector. Preferably a plasmid is a closed circular DNA molecule. 0016 Cytomegalovirus promoter refers to one or more sequences from a cytomegalovirus which are functional in eukaryotic cells as a transcriptional promoter and an upstream enhancer sequence. The enhancer sequence allows transcription to occur at a higher frequency from the associated promoter. 0017 In this context, transcriptionally linked means that in a system suitable for transcription, transcription will initiate under the direction of the control sequence(s) and proceed through sequences which are transcriptionally linked with that control sequence(s). Preferably no mutation is created in the resulting transcript, which would alter the resulting translation product. 0018 The term coding region or coding sequence refers to a nucleic acid sequence which encodes a particular gene product for which expression is desired, according to the normal base pairing and codon usage relationships. Thus, the coding sequence must be placed in such relationship to transcriptional control sequences (possibly including control elements and translational initiation and termination codons) that a proper length transcript will be produced and will result in translation in the appropriate reading frame to produce a functional desired product. 0019 In a preferred embodiment the interferon alpha coding sequence is for human interferon alpha and preferably is a synthetic sequence having optimal codon usage, such as the nucleotide sequence of SEQ ID NO:11 or semi-optimal codon usage, such as the nucleotide sequence of SEQ ID NO:12. 0020 A particular example of coding regions suitable for use in the plasmids of this invention are the natural sequences coding for human interferon alpha. Thus, in a preferred embodiment coding region has a nucleotide sequence which is the same as SEQ ID NO:10, which is the natural nucleotide sequence encoding human interferon alpha. However, it may be preferable to have an interferon alpha coding sequence which is a synthetic coding sequence. In a preferred embodiment, the interferon alpha coding sequence is a synthetic sequence utilizing optimal or semi-optimal codon usage, preferably the sequence shown in SEQ ID NO:11 or SEQ ID NO:12. 0021 Thus, a sequence coding for the human interferon alpha or a human interferon alpha coding sequence is a nucleic acid sequence which encodes the amino acid sequence of human interferon alpha, based on the normal base pairing and translational codon usage relationships. It is preferable that the coding sequence encode the exact, full amino acid sequence of natural human interferon, but this is not essential. The encoded polypeptide may differ from natural human interferon alpha, so long as the polypeptide retains interferon alpha activity, preferably the polypeptide is at least 50%, 75%, 90%, or 97% as active as natural human interferon alpha, and more preferably fully as active as natural human interferon alpha. Thus, the polypeptide encoded by the interferon alpha coding sequence may differ from a natural human interferon alpha polypeptide by a small amount, preferably less than a 15%, 10%, 5%, or 1% change. Such a change may be of one of more different types, such as deletion, addition, or substitution of one or more amino acids. 0022 The term transcriptional control sequence refers to sequences which control the rate of transcription of a transcriptionally linked coding region. Thus, the term can include elements such as promoters, operators, and enhancers. For a particular transcription unit, the transcriptional control sequences will include at least a promoter sequence. 0023 A growth hormone 3 untranslated region is a sequence located downstream (i.e., 3) of the region encoding material polypeptide and including at least part of the sequence of the natural 3 UTR/poly(a) signal from a growth hormone gene, preferably the human growth hormone gene. This region is generally transcribed but not translated. For expression in eukaryotic cells it is generally preferable to include sequence which signals the addition of a poly-A tail. As with other synthetic genetic elements a synthetic 3 UTR/poly(A) signal has a sequence which differs from naturally-occurring UTR elements. 0024 The sequence may be modified, for example by the deletion of ALU repeat sequences. Deletion of such ALU repeat sequences acts to reduce the possibility of homologous recombination between the expression cassette and genomic material in a transfected cell. 0025 The plasmid preferably includes a promoter, a TATA box, a Cap site and a first intron and intron/exon boundary in appropriate relationship for expression of the coding sequence. The plasmid may also include a 5 mRNA leader sequence inserted between the promoter and the coding sequence and/or an intron/5 UTR from a chicken skeletal -actin gene. Also, the plasmid may have a nucleotide sequence which is the same as the nucleotide sequence of plasmid pIF0921, as shown in FIGS. 5A-E. 0026 The plasmid may also include: (a) a first transcription unit containing a first transcriptional control sequence transcriptionally linked with a first 5-untranslated region, a first intron, a first coding sequence, and a first 3-untranslated region/poly(A) signal, wherein the first intron is between the control sequence and the first coding sequence; and (b) a second transcription unit containing a second transcriptional control sequence transcriptionally linked with a second 5-untranslated region, a second intron, a second coding sequence, and a second 3-untranslated region/poly(A) signal, wherein the second intron is between the control sequence and the second coding sequence; wherein the first and second coding sequences contain a sequence having the sequence of SEQ ID NO:2, 3, 4 or 25 coding for a human IL-12 p40 subunit, and a sequence having the sequence of SEQ ID NO:6, 7, 8 or 24 coding for a human IL-12 p35 subunit. 0027 The term transcription unit or expression cassette refers to a nucleotide sequence which contains at least one coding sequence along with sequence elements which direct the initiation and termination of transcription. A transcription unit may however include additional sequences, which may include sequences involved in post-transcriptional or post-translational processes. In preferred embodiments, the first transcriptional control sequence or the second transcriptional control sequence contain one or more cytomegalovirus promoter sequences. The first and second transcriptional control sequences can be the same or different. 0028 A 5 untranslated region or 5 UTR refers to a sequence located 3 to promoter region and 5 of the downstream coding region. Thus, such a sequence, while transcribed, is upstream of the translation initiation codon and therefore is not translated into a portion of the polypeptide product. 0029 For the plasmids described herein, one or more of a promoter, 5 untranslated region (5 UTR), the 3 UTR/poly(A) signal, and introns may be a synthetic sequence. In this context the term synthetic means that the sequence is not provided directly by the sequence of a naturally occurring genetic element of that type but rather is an artificially created sequence (i.e., created by a person by molecular biological methods). While one or more portions of such a synthetic sequence may be the same as portions of naturally occurring sequences, the full sequence over the specified genetic element is different from a naturally occurring genetic element of that type. The use of such synthetic genetic elements allows the functional characteristics of that element to be appropriately designed for the desired function. 0030 Thus, a synthetic intron refers to a sequence which is not a naturally occurring intron sequence but which will be removed from an RNA transcript during normal post transcriptional processing. Such introns can be designed to have a variety of different characteristics, in particular such introns can be designed to have a desired strength of splice site. 0031 A subunit of a therapeutic molecule is a polypeptide or RNA molecule which combines with one or more other molecules to form a complex having the relevant pharmacologic activity. Examples of such complexes include homodimers and heterodimers as well as complexes having greater numbers of subunits. A specific example of a heterodimer is IL-12, having the p40 and p35 subunits. 0032 The p40 subunit is the larger of the two subunits of the IL-12 heterodimer. 0033 Thus, it is capable of association with p35 subunit to form a molecule having activities characteristic of IL-12. Human p40 has the amino acid sequence of SEQ ID NO:1. Those skilled in the art will recognize that the molecule may have a number of changes from that sequence, such as deletions, insertions or changes of one or a few amino acids, while still retaining IL-12 activity when associated with p35. Such active altered molecules are also regarded as p40. 0034 Conversely, the p35 subunit is the smaller of the two heterodimeric subunits of IL-12. For humans, p35 has the amino acid sequence of SEQ ID NO:5. As for p40, p35 may have a low level of alterations from that sequence while still being regarded as p35. 0035 A particular example of coding regions suitable for use in the plasmids of this invention are the natural sequences coding for the p40 and p35 subunits of human IL-12. Thus, in a preferred embodiment the first and second coding regions are coding regions for those sequences and are preferably in the order p40 then p35 in the 5 to 3 direction. 0036 Thus, a sequence coding for the p40 subunit of human IL-12 is a nucleic acid sequence which encodes the human p40 subunit as described above, based on the normal base pairing and translational codon usage relationships. The sequence coding for p35 subunit of human IL-12 is similarly defined. 0037 In a preferred embodiment the sequence coding for the p40 subunit of human IL-12 is 5 to the sequence coding for the p35 subunit of human IL-12. Those skilled in the art will appreciate that the interferon alpha, p35 subunit and p40 subunit may all be on a single transcription unit, that all three may be on separate transcription units, or that any two coding sequences may be on one transcription unit and the other coding sequence on another transcription unit. 0038 The plasmid may also contain an intron having variable splicing, a first coding sequence, and a second coding sequence, wherein the first and second coding sequences include a sequence having the sequence of SEQ ID NO:2, 3, 4 or 25 coding for a human IL-12 p40 subunit, and a sequence having the sequence of SEQ ID NO:6, 7, 8 or 24 coding for a human IL-12 p35 subunit. 0039 In a preferred embodiment, the plasmid also has: (a) a transcriptional control sequence transcriptionally linked with a first coding sequence and a second coding sequence; (b) a 5-untranslated region; (c) an intron 5 to the first coding sequence; (d) an alternative splice site 3 to the first coding sequence and 5 to the second coding sequence; and (e) a 3-untranslated region/poly(A) signal. The transcriptional control sequence preferably includes a cytomegalovirus promoter sequence. 0040 In a preferred embodiment, the plasmid also has: (a) a transcriptional control sequence transcriptionally linked with a first coding sequence, an IRES sequence, a second coding sequence, and a 3-untranslated region/poly(A) signal, wherein the IRES sequence is between the first coding sequence and the second coding sequence; and (b) an intron between the promoter and the first coding sequence; wherein the first and second coding sequences include a sequence having the sequence of SEQ ID NO:2, 3, 4 or 25 coding for a human IL-12 p40 subunit, and a sequence having the sequence of SEQ ID NO:6, 7, 8 or 24 coding for a human IL-12 p35 subunit. The transcriptional control sequence preferably includes a cytomegalovirus promoter sequence and the IRES sequence preferably is from an encephalomyocarditis virus. 0041 For delivery of coding sequences for gene expression, it is generally useful to provide a delivery composition or delivery system which includes one or more other components in addition to the nucleic acid sequences. Such a composition can, for example, aid in maintaining the integrity of the DNA and/or in enhancing cellular uptake of the DNA and/or by acting as an immunogenic enhancer, such as by the non-DNA components having an immuno-stimulatory effect of their own. 0042 Thus, in another aspect, the invention features a composition containing a plasmid as described above and a protective, interactive non-condensing compound (PINC). 0043 The PINC enhances the delivery of the nucleic acid molecule to mammalian cells in vivo, and preferably the nucleic acid molecule includes a coding sequence for a gene product to be expressed in the cell. In many cases, the relevant gene product is a polypeptide or protein. Preferably the PINC is used under conditions so that the PINC does not form a gel, or so that no gel form is present at the time of administration at about 30-40 C. Thus, in these compositions, the PINC is present at a concentration of 30% (w/v) or less. In certain preferred embodiments, the PINC concentration is still less, for example, 20% or less, 10% or less, 5% or less, or 1% or less. Thus, these compositions differ in compound concentration and functional effect from uses of these or similar compounds in which the compounds are used at higher concentrations, for example in the ethylene glycol mediated transfection of plant protoplasts, or the formation of gels for drug or nucleic acid delivery. In general, the PINCs are not in gel form in the conditions in which they are used as PINCs, though certain of the compounds may form gels under some conditions. 0044 In connection with the compounds and compositions of this invention, the term protects or protective refers to an effect of the interaction between such a compound and a nucleic acid such that the rate of degradation of the nucleic acid is decreased in a particular environment. Such degradation may be due to a variety of different factors, which specifically include the enzymatic action of a nuclease. The protective action may be provided in different ways, for example, by exclusion of the nuclease molecules or by exclusion of water. 0045 Some compounds which protect a nucleic acid and/or prolong the bioavailability of a nucleic acid may also interact or associate with the nucleic acid by intermolecular forces and/or valence bonds such as: Van der Waals forces, ion-dipole interactions, ion-induced dipole interactions, hydrogen bonds, or ionic bonds. These interactions may serve the following functions: (1) Stereoselectively protect nucleic acids from nucleases by shielding; (2) facilitate the cellular uptake of nucleic acid by piggyback endocytosis. Piggyback endocytosis is the cellular uptake of a drug or other molecule complexed to a carrier that may be taken up by endocytosis. CV Uglea and C Dumitriu-Medvichi, Medical Applications of Synthetic Oligomers, In: Polymeric Biomaterials, Severian Dumitriu ed., Marcel Dekker, Inc., 1993, incorporated herein by reference. 0046 To achieve the desired effects set forth it is desirable, but not necessary, that the compounds which protect the nucleic acid and/or prolong the bioavailability of a nucleic acid have amphiphilic properties; that is, have both hydrophilic and hydrophobic regions. The hydrophilic region of the compounds may associate with the largely ionic and hydrophilic regions of the nucleic acid, while the hydrophobic region of the compounds may act to retard diffusion of nucleic acid and to protect nucleic acid from nucleases. 0047 Additionally, the hydrophobic region may specifically interact with cell membranes, possibly facilitating endocytosis of the compound and thereby also of nucleic acid associated with the compound. This process may increase the pericellular concentration of nucleic acid. 0048 Agents which may have amphiphilic properties and are generally regarded as being pharmaceutically acceptable are the following: polyvinylpyrrolidones; polyvinylalcohols; polyvinylacetates; propylene glycol; polyethylene glycols; poloxamers (Pluronics); poloxamines (Tetronics); ethylene vinyl acetates; methylcelluloses, hydroxypropylcelluloses, hydroxypropylmethylcelluloses; heteropolysaccharides (pectins); chitosans; phosphatidylcholines (lecithins); miglyols; polylactic acid; polyhydroxybutyric acid; xanthan gum. Also, copolymer systems such as polyethylene glycol-polylactic acid (PEG-PLA), polyethylene glycol-polyhydroxybutyric acid (PEG-PHB), polyvinylpyrrolidone-polyvinylalcohol (PVP-PVA), and derivatized copolymers such as copolymers of N-vinyl purine (or pyrimidine) derivatives and N-vinylpyrrolidone. However, not all of the above compounds are protective, interactive, non-condensing compounds as described below. 0049 In connection with the protective, interactive, non-condensing compounds for these compositions, the term non-condensing means that an associated nucleic acid is not condensed or collapsed by the interaction with the PINC at the concentrations used in the compositions. Thus, the PINCs differ in type and/or use concentration from such condensing polymers. Examples of commonly used condensing polymers include polylysine, and cascade polymers (spherical polycations). 0050 Also in connection with such compounds and an associated nucleic acid molecule, the term enhances the delivery means that at least in conditions such that the amounts of PINC and nucleic acid is optimized, a greater biological effect is obtained than with the delivery of nucleic acid in saline. Thus, in cases where the expression of a gene product encoded by the nucleic acid is desired, the level of expression obtained with the PINC:nucleic acid composition is greater than the expression obtained with the same quantity of nucleic acid in saline for delivery by a method appropriate for the particular PINC/coding sequence combination. 0051 In preferred embodiments of the above compositions, the PINC is polyvinyl pyrrolidone (PVP), polyvinyl alcohol (PVA), a PVP-PVA co-polymer, N-methyl-2-pyrrolidone (NM2P), ethylene glycol, or propylene glycol. In compositions in which a Poloxamer (Pluronics) is used, the nucleic acid is preferably not a viral vector, i.e., the nucleic acid is a non-viral vector. 0052 In other preferred embodiments, the PINC is bound with a targeting ligand. Such targeting ligands can be of a variety of different types, including but not limited to galactosyl, residues, fucosal residues, mannosyl residues, camtitine derivatives, monoclonal antibodies, polyclonal antibodies, peptide ligands, and DNA-binding proteins. The targeting ligands may bind with receptors on cells such as antigen-presenting cells, hepatocytes, myocytes, epithelial cells, endothelial cells, and cancer cells. 0053 In connection with the association of a targeting ligand and a PINC, the term bound with means that the parts have an interaction with each other such that the physical association is thermodynamically favored, representing at least a local minimum in the free energy function for that association. Such interaction may involve covalent binding, or non-covalent interactions such as ionic, hydrogen bonding, van der Waals interactions, hydrophobic interactions, and combinations of such interactions. 0054 While the targeting ligand may be of various types, in one embodiment the ligand is an antibody. Both monoclonal antibodies and polyclonal antibodies may be utilized. 0055 The nucleic acid may also be present in various forms. Preferably the nucleic acid is not associated with a compounds(s) which alter the physical form, however, in other embodiments the nucleic acid is condensed (such as with a condensing polymer), formulated with cationic lipids, formulated with peptides, or formulated with cationic polymers. 0056 In preferred embodiments, the protective, interactive non-condensing compound is polyvinyl pyrrolidone, and/or the plasmid is in a solution having between 0.5% and 50% PVP, more preferably about 5% PVP. The DNA preferably is at least about 80% supercoiled, more preferably at least about 90% supercoiled, and most preferably at least about 95% supercoiled. 0057 In another aspect the invention features a composition containing a protective, interactive non-condensing compound and a plasmid containing an interferon alpha coding sequence. 0058 In yet another aspect, the invention provides a composition containing a plasmid of the invention (or a plasmid containing an interferon alpha coding sequence) and a cationic lipid with a neutral co-lipid. 0059 Preferably the cationic lipid is DOTMA and the neutral co-lipid is cholesterol (chol). DOTMA is 1,2-di-O-octadecenyl-3-trimethylammonium propane, which is described and discussed in Eppstein et al., U.S. Pat. No. 4,897,355, issued Jan. 30, 1990, which is incorporated herein by reference. However, other lipids and lipid combinations may be used in other embodiments. A variety of such lipids are described in Gao & Huang, 1995, Gene Therapy 2:710-722, which is hereby incorporated by reference. 0060 As the charge ratio of the cationic lipid and the DNA is also a significant factor, in preferred embodiments the DNA and the cationic lipid are present is such amounts that the negative to positive charge ratio is about 1:3. While preferable, it is not necessary that the ratio be 1:3. Thus, preferably the charge ratio for the compositions is between about 1:1 and 1:10, more preferably between about 1:2 and 1:5. 0061 The term cationic lipid refers to a lipid which has a net positive charge at physiological pH, and preferably carries no negative charges at such pH. An example of such a lipid is DOTMA. Similarly, neutral co-lipid refers to a lipid which has is usually uncharged at physiological pH. An example of such a lipid is cholesterol. 0062 Thus, negative to positive charge ratio for the DNA and cationic lipid refers to the ratio between the net negative charges on the DNA compared to the net positive charges on the cationic lipid. 0063 As the form of the DNA affects the expression efficiency, the DNA preferably is at least about 80% supercoiled, more preferably at least about 90% supercoiled, and most preferably at least about 95% supercoiled. The composition preferably includes an isotonic carbohydrate solution, such as an isotonic carbohydrate solution that consists essentially of about 10% lactose. In preferred embodiments, the composition the cationic lipid and the neutral co-lipid are prepared as a liposome having an extrusion size of about 800 nanometers. Preferably the liposomes are prepared to have an average diameter of between about 20 and 800 nm, more preferably between about 50 and 400 nm, still more preferably between about 75 and 200 nm, and most preferably about 100 nm. Microfluidization is the preferred method of preparation of the liposomes. 0064 In another aspect the invention features a composition containing: (a) a first component having a plasmid including an interferon alpha coding sequence and a cationic lipid with a neutral co-lipid, wherein the cationic lipid is DOTMA and the neutral co-lipid is cholesterol, wherein the DNA in the plasmid and the cationic lipid are present in amounts such that the negative to positive charge ratio is about 1:3; and (b) a second component including a protective, interactive non-condensing compound, wherein the first component is present within the second component. 0065 In another aspect, the invention provides a composition having a protective, interactive non-condensing compound, a first plasmid including an interferon alpha coding sequence, and one or more other plasmids independently having an IL-12 p35 or IL-12 p40 subunit coding sequence. 0066 In another aspect, the invention features a method for making any of the plasmids described above by inserting a CMV promoter transcriptionally linked with an interferon alpha coding sequence, and a growth hormone 3-untranslated region into a plasmid. 0067 The invention also provides methods of making the compositions described above. The method may involve: (a) preparing a DNA molecule having a transcriptional unit, wherein the transcriptional unit contains an interferon alpha coding sequence; (b) preparing a protective, interactive non-condensing compound; and (c) combining the protective, interactive non-condensing compound with the DNA in conditions such that a composition capable of delivering a therapeutically effective amount of an interferon alpha coding sequence to a mammal is formed. 0068 Preferably, the DNA molecule is a plasmid, wherein the plasmid includes a CMV promoter transcriptionally linked with an interferon alpha coding sequence, and a human growth hormone 3-untranslated region/poly(A) signal. 0069 The method may involve the steps of: (a) preparing a DNA having an interferon alpha coding sequence; (b) preparing a mixture of a cationic lipid and a neutral co-lipid, wherein the cationic lipid is DOTMA and the neutral co-lipid is cholesterol; and (c) combining the mixture with the DNA in amounts such that the cationic lipid and the DNA are present in a negative to positive charge ratio of about 1:3. 0070 In another embodiment, the method involves the steps of: (a) preparing a first component having a plasmid containing an interferon alpha coding sequence and a cationic lipid with a neutral co-lipid, wherein the cationic lipid is DOTMA and the neutral co-lipid is cholesterol, wherein the DNA in the plasmid and the cationic lipid are present in amounts such that the negative to positive charge ratio is about 1:3; (b) preparing a second component having a protective, interactive non-condensing compound; and (c) combining the first and second components such that the resulting composition includes the first component within the second component. 0071 In another embodiment, the method involves the steps of: (a) preparing a protective, interactive non-condensing compound, (b) preparing a first plasmid having an interferon alpha coding sequence, (c) preparing one or more other plasmids independently having an IL-12 p35 or IL-12 p40 subunit coding sequence, and (d) combining the protective, interactive non-condensing compound, the plasmid having the interferon alpha coding sequence and the other plasmids. 0072 In another aspect, the invention provides a method for treatment of a mammalian condition or disease, by administering to a mammal suffering from the condition or disease a therapeutically effective amount of a plasmid as described herein. 0073 A therapeutically effective amount of a composition is an amount which is sufficient to cause at least temporary relief or improvement in a symptom or indication of a disease or condition. Thus, the amount is also sufficient to cause a pharmacological effect. The amount of the composition need not cause permanent improvement or improvement of all symptoms or indications. A therapeutically effective amount of a cancer therapeutic would be one that reduces overall tumor burden in the case of metastatic disease (i.e., the number of metasteses or their size) or one that reduces the mass of the tumor in localized cancers. 0074 The condition or disease preferably is a cancer, such as epithelial glandular cancer, including adenoma and adenocarcinoma; squamous and transitional cancer, including polyp, papilloma, squamous cell and transitional cell carcinoma; connective tissue cancer, including tissue type positive, sarcoma and other (oma's); hematopoietic and lymphoreticular cancer, including lymphoma, leukemia and Hodgkin's disease; neural tissue cancer, including neuroma, sarcoma, neurofibroma and blastoma; mixed tissues of origin cancer, including teratoma and teratocarcinoma. Other cancerous conditions that are applicable to treatment include cancer of any of the following: adrenal gland, anus, bile duct, bladder, brain tumors: adult, breast, cancer of an unknown primary site, carcinoids of the gastrointestinal tract, cervix, childhood cancers, colon and rectum, esophagus, gall bladder, head and neck, islet cell and other pancreatic carcinomas, Kaposi's sarcoma, kidney, leukemia, liver, lung: non-small cell, lung: small cell, lymphoma: AIDS-associated, lymphoma: Hodgkin's disease, Lymphomas: non-Hodgkin's disease, melanoma, mesothelioma, metastatic cancer, multiple myeloma, ovary, ovarian germ cell tumors, pancreas, parathyroid, penis, pituitary, prostate, sarcomas of bone and soft tissue, skin, small intestine, stomach, testis, thymus, thyroid, trophoblastic disease, uterus: endometrial carcinoma, uterus: uterine sarcomas, vagina, or vulva. The composition preferably is administered by injection, although the method may also be performed ex vivo. 0075 In another aspect, the invention provides a method for transfection (i.e., the delivery and expression of a gene to cells) of a cell in situ, by contacting the cell with a plasmid described herein for sufficient time to transfect the cell. Transfection of the cell preferably is performed in vivo and the contacting preferably is performed in the presence of about 5% PVP solution. 0076 In another aspect, the invention features a method for delivery and expression of an interferon alpha gene in a plurality of cells, by: (a) transfecting the plurality of cells with a plasmid or composition of the invention; and (b) incubating the plurality of cells under conditions allowing expression of a nucleic acid sequence in the vector, wherein the nucleic acid sequence encodes interferon alpha. 0077 In preferred embodiments, the interferon alpha is human interferon alpha and the cells are human cells and/or the contacting is performed in the presence of an about 5% PVP solution. 0078 In another aspect, the invention features a method for treating a disease or condition, by transfecting a cell in situ with a plasmid or composition of the invention. The disease or condition can be a localized disease or condition or a systemic disease or condition. 0079 In another aspect, the invention features a cell transfected with a plasmid or composition of the invention. 0080 In yet another aspect, the invention features a method for treatment of a mammalian condition or disease, by administering to a mammal suffering from the condition or disease a therapeutically effective amount of a composition described herein. 0081 As the compositions are useful for delivery of a nucleic acid molecule to cells in vivo, in a related aspect the invention provides a composition at an in vivo site of administration. In particular this includes at an in vivo site in a mammal. 0082 In preferred embodiments the nucleic acid molecule includes a sequence encoding a gene product. Also in preferred embodiments, the site of administration is in an interstitial space or a tissue of an animal, particularly of a mammal. 0083 The invention also provides methods for using the above compositions. Therefore, in further related aspects, methods of administering the compositions are provided in which the composition is introduced into a mammal, preferably into a tissue or an interstitial space. 0084 Various methods of delivery may be utilized, such as are known in the art, but in preferred embodiments, the composition is introduced into the tissue or interstitial space by injection. The compositions may also be delivered to a variety of different tissues, but in preferred embodiments the tissue is muscle or tumor. 0085 In another related aspect, the invention provides methods for treating a mammalian condition or disease by administering a therapeutically effective amount of a composition as described above. In preferred embodiments, the disease or condition is a cancer. 0086 The summary of the invention described above is non-limiting and other features and advantages of the invention will be apparent from the following detailed description of the preferred embodiments, as well as from the claims.

BRIEF DESCRIPTION OF THE DRAWINGS 0087 FIG. 1 shows the effects of interferon alpha in two cancer models. 0088 FIGS. 2A-E show a plasmid map and sequence (SEQ ID NO:18) for an exemplary IL-12 plasmid of the present invention. 0089 FIGS. 3A-B show optimal codon usage for highly expressed human genes. 0090 FIGS. 4A-C show a plasmid map and sequence (SEQ ID NO:19) for plasmid pIF0836, an exemplary interferon alpha plasmid of the present invention. 0091 FIGS. 5A-E show a plasmid map and sequence (SEQ ID NO:20) for pIN096, an exemplary IL-12 plasmid that can be used with the present invention. 0092 FIGS. 6A-B show the nucleic acid sequence (SEQ ID NO:21) of plasmid pIF0921, an exemplary interferon alpha plasmid of the present invention. 0093 FIGS. 7A-B show a plasmid map and sequence (SEQ ID NO:22) for plasmid pIF0921. 0094 FIG. 8 shows an outline of a strategy that can be used to synthesize a pIF0921 plasmid. 0095 FIG. 9 shows interferon alpha and IL-12 gene medicine (combination therapy) in Renca model.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS 0096 The present invention relates to gene delivery and gene therapy, and provides novel nucleic acid constructs for expression of interferon alpha in a mammal, formulations for delivery that incorporate a nucleic acid construct for expression, and methods for preparing and using such constructs and formulations. In particular, this invention relates to plasmid constructs for delivery of therapeutic interferon alpha encoding nucleic acids to cells in order to modulate tumor activity, methods of using those constructs (including combination therapy with other agents, such as cytokines, preferably IL-12), as well as methods for preparing such constructs. 0097 I. General 0098 As described, this invention concerns expression systems for the delivery and expression of interferon alpha coding sequences in mammalian cells, and formulations and methods for delivering such expression systems or other expression systems to a mammal. 0099 Therefore, particular genetic constructs are described which includes nucleotide sequences coding for interferon alpha, preferably human interferon alpha. Such a construct can beneficially be formulated and administered as described herein, utilizing the expression systems of this invention. 0100 To allow convenient production of such plasmids, it is generally preferable that the plasmid be capable of replication in a cell to high copy number. Generally such production is carried out in prokaryotic cells, particularly including Esherichia coli (E.coli) cells. Thus, the plasmid preferably contains a replication origin functional in a prokaryotic cell, and preferably the replication origin is one which will direct replication to a high copy number. 0101 It is also possible to utilize synthetic genetic elements in the plasmid constructs. 0102 As described below, these elements affect post-transcriptional processing in eukaryotic systems. Thus, the use of synthetic sequences allows the design of processing characteristics as desired for the particular application. Commonly, the elements will be designed to provide rapid and accurate processing. 0103 For delivery of DNA encoding a desired expression product to a mammalian system, it is usually preferable to utilize a delivery system. Such a system can provide multiple benefits, notably providing stabilization to protect the integrity of the DNA, as well as assisting in cellular uptake. 0104 In addition, the non-DNA components of the formulation may contribute to an immune system enhancement or activation. As a result, components of a delivery system can be selected in conjunction with a particular gene product to enhance or minimize the immuno-stimulatory effect. 0105 The plasmids may also include elements for expression of IL-12 or one or more subunits thereof. Similarly, the treatment may involve administration of an interferon alpha coding sequence and one or more IL-12 coding sequences whether on a single plasmid or on separate plasmids. Such plasmids may be incorporated into compositions for delivery with a protective, interactive non-condensing compound, a cationic lipid and neutral co-lipid, or both. 0106 While these are specific effective examples, other components may be utilized in formulations containing the interferon alpha expression vectors of the present invention to provide effective delivery and expression of interferon alpha or with other coding sequences for which manipulation of the activation of immune system components is desirable. 0107 The selection of delivery system components and preparation methods in conjunction with the selection of coding sequences provides the ability to balance the specific effects of the encoded gene products and the immune system effects of the overall delivery system composition. This capacity to control the biological effects of delivery system formulation administration represents an aspect of the invention in addition to the interferon alpha encoding constructs and specific formulations of delivery systems. Co-selection of the encoded gene product and the delivery system components and parameters provides enhanced desired effects rather than merely providing high level gene expression. In particular, such enhancement is described below for the antitumor effects of the exemplary PVP containing compositions. 0108 For systems in which IL-12 is also administered, the antitumor effect can be greater than merely additive (i.e., greater than merely the sum of the antitumor effects of interferon alpha alone and IL-12 alone). Enhancement of immuno-stimulatory effects is also desirable in other contexts, for example, for vaccine applications. 0109 In contrast, for certain applications, it is preferable to select a delivery systems which minimizes the immune system effects. For example, it is often preferred that the immune system activation be minimized for compositions to be delivered to the lung in order to minimize lung tissue swelling. 0110 a useful approach for selecting the delivery system components and preparation techniques for a particular coding sequence can proceed as follows, but is not limited to these steps or step order. 0111 1. Select a particular genetic construct which provides appropriate expression in vitro. 0112 2. Select delivery system components based on desired immuno-stimulatory effects and/or on in vivo physiological effect. Such effects can be tested or verified in in vivo model systems. 0113 3. Select the other delivery system parameters consistent with the desired immuno-stimulatory effects and/or consistent with enhancing the desired in vivo physiological effect. Such parameters can, for example, include the amount and ratio of DNA to one or more other composition components, the relative amounts of non-DNA composition components, the size of delivery system formulation particles, the percent supercoiled DNA for circular dsDNA vectors, and the specific method of preparation of delivery system formulation particles. The particular parameters relevant for specific types of formulations will be apparent or readily determined by testing. 0114 The description below illustrates the selection of components and parameters in the context of interferon alpha encoding constructs. However, it should be recognized that the approach is applicable to constructs containing a variety of other coding sequences. 0115 II. Plasmid Construct Expression Systems 0116 A. Plasmid Design and Construction 0117 For the methods and constructs of this invention, a number of different plasmids were constructed which are useful for delivery and expression of sequences encoding interferon alpha. Thus, these plasmids contain coding regions for interferon alpha, along with genetic elements necessary or useful for expression of those coding regions. 0118 While these embodiments utilized interferon alpha cDNA clones or partial genomic sequences from a particular source, those skilled in the art could readily obtain interferon alpha coding sequences from other sources, or obtain a coding sequence by identifying a cDNA clone in a library using a probe(s) based on the published interferon alpha coding and/or flanking sequences. This also applies to the IL-12 coding sequences utilized in the embodiments described herein. 0119 Coding sequences for interferon alpha were incorporated into an expression plasmid that contains eukaryotic and bacterial genetic elements. Eukaryotic genetic elements include the CMV immediate early promoter and 5 UTR, and a human growth hormone 3 UTR/poly(a) signal, which influence gene expression by controlling the accuracy and efficiency of RNA processing, mRNA stability, and translation. 0120 The human growth hormone 3 UTR is from a human growth hormone gene, and preferably includes a poly(a) signal. This sequence can be linked immediately following the natural translation termination codon for a cDNA sequence, genomic sequence, modified genomic sequence, or synthetic sequence coding for interferon alpha. 0121 An example of a human growth hormone 3 UTR/poly(a) signal is shown by the human growth hormone 3 UTR (nucleotides 1-100) and 3 flanking sequence (nucleotides 101-191; GenBank accession J03071, HUMGHCSA) below. (SEQ ID NO:13) 11GGGTGGCATCCCTGTGACCCCTCCCCAGTGCCTCTCCTGGCCCTGGAAGTPoly (a)signal 51TGCCACTCCAGTGCCCACCAGCCTTGTCCTAATAAAATTAAGTTGCATCA 101TTTTGTCTGACTAGGTGTCCTTCTATAATATTATGGGGTGGAGGGGGGTG 151GTATGGAGCAAGGGGCAAGTTGGGAAGACAACCTGTAGGGC

0122 The 5 and 3 UTR and flanking regions can be further and more precisely defined by routine methodology, e.g., deletion or mutation analysis or their equivalents., and can be modified to provide other sequences having appropriate transcriptional and translational functions. 0123 1. Construction of plasmid: Plasmid Backbone, human interferon alpha cDNA, Final Construct 0124 a diagrammatic representation of the PCR products and plasmids involved in creation of an exemplary construct is shown below in FIG. 8. 0125 Plasmid pIF0921 was constructed from commercially available plasmids, and contains the TN5 gene encoding the kanamycin resistance gene, the pUC origin of replication, the CMV enhancer and promoter to base 112, a synthetic intron called IVS8, the human IFN-a 2b gene, and the human growth hormone 3 UTR. The plasmid construction descendancy for pIL0697 is shown in FIG. 8. pIL0697 was cut with BamHI and Xba I and the hIFN-a2b PCR product, which had been amplified from human genomic DNA with BamHI and Xba I ends, was cloned into the pIL0697 backbone in place of the IL-2 coding region. The resulting plasmid was pIF0863. pIF0863 was cut with Nco I and intron IVS8 from pCT0828 was cloned in. The resulting plasmid was pIF0890. pIF0890 was cut with Nde I and Pac I and an additional region of the CMV 5 UTR to base 112 was cloned in from plasmid pLC0888. 0126 B. Synthetic Genetic Elements 0127 In some embodiments, some or all of the genetic elements can be synthetic, derived from synthetic oligonucleotides, and thus are not obtained directly from natural genetic sequences. These synthetic elements are appropriate for use in many different expression vectors. 0128 A synthetic intron is designed with splice sites that ensure that RNA splicing is accurate and efficient. A synthetic 3 UTR/poly(A) signal is designed to facilitate mRNA 3 end formation and mRNA stability. A synthetic 5 UTR is designed to facilitate the initiation of translation. The design of exemplary synthetic elements is described in more detail below. 0129 1. Summary of Synthetic Element Features 0130 Exemplary synthetic 5UTR, intron, and 3UTR/poly(A) signal have the general features shown below: 25 UTRShort.Lack of secondary structure.Kozak sequence.Site for intron insertion.Intron5 splice site sequence matches consensus.5 splice site sequence is exactlycomplementary to 5 end of U1 snRNA.Branch point sequence matches consensus.Branch point sequence is complementary to U2snRNA.3 splice site matches consensus.Polypyrimidine tract is 16 bases in length andcontains 7 consecutive T's.(The tract preferably contains at least 5consecutive T's.)Contains internal restriction enzyme sites.BbsI cleaves at the 5ss, EarI cleaves at the3ss.3 UTR/Poly(A)Based on rabbit -globin 3 UTR/poly(A)signal.Consists of two poly(A) signals in tandem.

0131 2. Features of the Synthetic 5UTR (UT6): 0132 The 5 untranslated region (5UTR) influences the translational efficiency of messenger RNA, and is therefore an important determinant of eukaryotic gene expression. The synthetic 5UTR sequence (UT6) has been designed to maximize the translational efficiency of mRNAs encoded by vectors that express genes of therapeutic interest. 0133 The sequence of the synthetic 5 UTR (UT6) is shown below. The Kozak sequence is in boldface and the initiation codon is double underlined. The location of the intron (between residues 48 and 49) is indicated by the filled triangle and the sequences that form the exonic portion of consensus splice sites are single underlined. The restriction sites for HindIII and NcoI are overlined. (SEQ ID NO:14) 3``HindIII``AAGCTTACTCAACACAATAACAAACTTACTTACAATCTTAATTAACAGGC ````NcoI```CACCATGG

0134 The 5 untranslated region (5 UTR), located between the cap site and initiation codon, is known to influence the efficiency of mRNA translation. Any features that influence the accessibility of the 5 cap structure to initiation factors, the binding and subsequent migration of the 43S preinitiation complex, or the recognition of the initiation codon, will influence mRNA translatability. An efficient 5 UTR is expected to be one that is moderate in length, devoid of secondary structure, devoid of upstream initiation codons, and has an AUG within an optimal local context (Kozak, 1994, Biochimie 76:815-821; Jansen et al., 1994). A 5 UTR with these characteristics should allow efficient recognition of the 5 cap structure, followed by rapid and unimpeded ribosome scanning by the ribosome, thereby facilitating the translation initiation process. 0135 The sequence of the synthetic 5UTR was designed to be moderate in length (54 nucleotides (nts)), to be deficient in G but rich in C and A residues, to lack an upstream ATG, to place the intended ATG within the context of a optimal Kozak sequence (CCACCATGG), and to lack potential secondary structure. The synthetic 5 UTR sequence was also designed to lack AU-rich sequences that target mRNAs to be rapidly degraded in the cytoplasm. 0136 Experiments have demonstrated that introns increase gene expression from cDNA vectors, and that introns located in the 5 UTR are more effective than ones located in the 3 UTR (Huang and Gorman, 1990, Mol. Cell. Biol. 10:1805-1810; Evans and Scarpulla, 1989, Gene 84:135-142; Brinster et al., 1988, Proc. Natl. Acad. Sci. USA 85:836-840; Palmiter et al., 1991, Proc. Natl. Acad. Sci. USA 88:478-482; Choi et al., 1991, Mol. Cell. Biol. 11:3070-3074). Accordingly, the synthetic 5 UTR sequence was designed to accommodate an intron with consensus splice site sequences. The intron may, for example, be located between residues 48 and 49 (See intron sequence structure below). The CAG at position 46-48 is the exonic portion of a consensus 5 splice site. The G at position 49 is the exonic portion of a consensus 3 splice site. 0137 To facilitate cloning manipulations, the synthetic 5 UTR sequence was designed to begin with a HindIII site and terminate with a NcoI site. 0138 3. Features of the Synthetic Intron 0139 RNA splicing is required for the expression of most eukaryotic genes. For optimal gene expression, RNA splicing must be highly efficient and accurate. A synthetic intron, termed OPTIVS8B, was designed to be maximally efficient and accurate. 0140 The structure of the exemplary synthetic intron, OPTIVS8 is shown below. Sequences for the 5 splice site (5ss), branch point (bp), and 3 splice site (3ss) are double underlined. The recognition sequences for the restriction enzymes BbsI and Earl are overlined. The cleavage site for BbsI corresponds to the 5ss, and the cleavage site for Earl corresponds to the 3ss. 45ssbp3ssBbsIEarI5CAGGTAAGTGTCTTC---(77)---TACTAACGGTTCTTTTTTTCTCTTCACAGG3(SEQ ID NO.15)(SEQ ID NO.16)

0141 The 5 splice site (5ss) sequence matches the established consensus sequence, MAG 9 GTRAGT, where MC or A, and RG or A. Since the mechanism of splicing involves an interaction between the 5ss of the pre-mRNA and U1 snRNA, the 5ss sequence of OPTIVS8B was chosen to be exactly complementary to the 5 end of U1 snRNA. 55ss U1 RNA

BP U2 RNA

0142 The sequence of the 3 splice site (3ss) matches the established consensus sequence, Y11NYAG 9 G, where YC or T, and Nany base. In 3 splice sites, the polypyrimidine tract (Y11) is the major determinant of splice site strength. For optimal splice site function in OPTIVS8B, the length of the polypyrimidine tract was extended to 16 bases, and its sequence was adjusted to contain 7 consecutive T residues. This feature was included because Roscigno et al. (1993) demonstrated that optimal splicing requires the presence of at least 5 consecutive T residues in the polypyrimidine tract. 0143 Splicing in vitro is generally optimal when introns are >80 nts in length (Wieringa, et al., 1984; Ulfendahl et al., 1985, Nucl. Acids Res. 13:6299-6315). Although many introns may be thousands of bases in length, most naturally occurring introns are 90-200 nt in length (Hawkins, 1988, Nucl. Acids Res. 16:9893-9908). The length of the synthetic intron (118 nts) falls within this latter range. 0144 OPTIVS8B was designed with three internal restriction enzyme sites, BbsI, NheI, and Earl. These restriction sites facilitate the screening and identification of genes that contain the synthetic intron sequence. In addition, the BbsI and Earl sites were placed so that their cleavage sites exactly correspond to the 5ss (BbsI) or 3ss (Earl). The sequence of the polypyrimidine tract was specifically designed to accommodate the Earl restriction site. Inclusion of the BbsI and Earl sites at these locations is useful because they permit the intron to be precisely deleted from a gene. They also permit the generation of an intron cassette that can be inserted at other locations within a gene. 0145 The 77 bases between the BbsI site and the branch point sequence are random in sequence, except for the inclusion of the NheI restriction site. 0146 4. Features of the Synthetic 3 UTR/poly(A) Signal: 0147 The 3 ends of eukaryotic mRNAs are formed by the process of polyadenylation. This process involves site specific site RNA cleavage, followed by addition of a poly(A) tail. RNAs that lack a poly(A) tail are highly unstable. Thus, the efficiency of cleavage/polyadenylation is a major determinant of mRNA levels, and thereby, of gene expression levels. 2XPA1 is a synthetic sequence, containing two efficient poly(A) signals, that is designed to be maximally effective in polyadenylation. 0148 A poly(A) signal is required for the formation of the 3 end of most eukaryotic mRNA. The signal directs two RNA processing reactions: site-specific endonucleolytic cleavage of the RNA transcript, and stepwise addition of adenylates (approximately 250) to the newly generated 3 end to form the poly(A) tail. A poly(A) signal has three parts: hexanucleotide, cleavage site, and downstream element. The hexanucleotide is typically AAUAAA and cleavage sites are most frequently 3 to the dinucleotide CA (Sheets et al., 1987). Downstream elements are required for optimal poly(A) signal function and are located downstream of the cleavage site. The sequence requirement for downstream elements is not yet fully established, but is generally viewed as UG- or U-rich sequences (Wickens, 1990; Proudfoot, 1991, Cell 64:671-674; Wahle, 1992, Bioessays 14:113-118; Chen and Nordstrom, 1992, Nucl. Acids Res. 20:2565-2572). 0149 Naturally occurring poly(A) signals are highly variable in their effectiveness (Peterson, 1992). The effectiveness of a particular poly(A) signal is mostly determined by the quality of the downstream element. (Wahle, 1992). In expression vectors designed to express genes of therapeutic interest, it is important to have a poly(A) signal that is as efficient as possible. 0150 Poly(A) efficiency is important for gene expression, because transcripts that fail to be cleaved and polyadenylated are rapidly degraded in the nuclear compartment. In fact, the efficiency of polyadenylation in living cells is difficult to measure, since nonpolyadenylated RNAs are so unstable. In addition to being required for mRNA stability, poly(A) tails contribute to the translatability of mRNA, and may influence other RNA processing reactions such as splicing or RNA transport ((Jackson and Standart, 1990, Cell 62:15-24; Wahle, 1992). 0151 Some eukaryotic genes have more than one poly(A) site, implying that if the cleavage/polyadenylation reaction fails to occur at the first site, it will occur at one of the later sites. In COS cell transfection experiments, a gene with two strong poly(A) sites yielded approximately two-fold more mRNA than one with a single strong poly(A) site (Bordonaro, 1995). These data suggest that a significant fraction of transcripts remain unprocessed even with a single efficient poly(A) signal. Thus, it may be preferable to include more than one poly(A) site. 0152 The sequence of the exemplary synthetic poly(A) signal is shown below. The sequence is named 2XPA. The hexanucleotide sequences and downstream element sequences are double underlined, and the two poly(A) sites are labeled as pA1 and pA2. Convenient restriction sites are overlined. The entire 2XPA unit may be transferred in cloning experiments as a XbaI-KpnI fragment. Deletion of the internal BspHI fragment results in the formation of a 1XPA unit. (SEQ ID NO.17) 6XbaIBspHITCTAGAGCATTTTTCCCTCTGCCAAAAATTATGGGGACATCATGAAGCCCCTTGAGCATCTGACG pA1HexDownstream elementTCTGGCTAATAAAGGAAATTTATTTTCATTGCAATAGTGTGTTGGAATTTTTTGTGTCTCTCACT +E,usn BspHICGGTACTAGAGCATTTTTCCCTCTGCCAAAAATTATGGGGACATCATGAAGCCCCTTGAGCATCT pA2HexDownstream elementGACGTCTGGCTAATAAAGGAAATTTATTTTCATTGCAATAGTGTGTTGGAATTTTTTGTGTCTCT KpnICACTCGGTACC

0153 The sequence of the synthetic poly(A) site shown above is based on the sequence of the rabbit -globin poly(A) signal, a signal that has been characterized in the literature as strong (Gil and Proudfoot, 1987, Cell 49:399-406; Gil and Proudfoot, 1984, Nature 312:473-474). One of its key features is the structure of its downstream element, which contains both UG- and U-rich domains. 0154 A double-stranded DNA sequence corresponding to the 1XPA sequence was constructed from synthetic oligonucleotides. Two copies of the 1XPA sequence were then joined to form the 2XPA sequence. The sequences were joined in such as way as to have a unique XbaI site at the 5 end of the first poly(A) signal containing fragment, and a unique KpnI site at the 3 end of the second poly(A) signal containing fragment. 0155 C. Interferon Alpha and IL-12 Coding Sequences 0156 The nucleotide sequence of a natural human interferon alpha coding sequences is known, and is provided below, along with a synthetic sequence which also codes for human interferon alpha. The same applies with respect to the IL-12 coding sequences. 0157 In some cases, instead of the natural sequence coding for interferon alpha, it is advantageous to utilize synthetic sequences which encode interferon alpha. Such synthetic sequences have alternate codon usage from the natural sequence, and thus have dramatically different nucleotide sequences from the natural sequence. In particular, synthetic sequences can be used which have codon usage at least partially optimized for expression in a human. The natural sequences do not have such optimal codon usage. Preferably, substantially all the codons are optimized. 0158 Optimal codon usage in humans is indicated by codon usage frequencies for highly expressed human genes, as shown in FIGS. 3A-B. The codon usage chart is from the program Human_High.cod from the Wisconsin Sequence Analysis Package, Version 8.1, Genetics Computer Group, Madison, Wis. The codons which are most frequently used in highly expressed human genes are presumptively the optimal codons for expression in human host cells, and thus form the basis for constructing a synthetic coding sequence. An example of a synthetic interferon alpha coding sequence is shown as the bottom sequence in the table below. 0159 However, rather than a sequence having fully optimized codon usage, it may be desirable to utilize an interferon alpha encoding sequence which has optimized codon usage except in areas where the same amino acid is too close together or abundant to make uniform codon usage optimal. 0160 In addition, other synthetic sequences can be used which have substantial portions of the codon usage optimized, for example, with at least 50%, 70%, 80% or 90% optimized codons as compared to a natural coding sequence. Other particular synthetic sequences for interferon alpha can be selected by reference to the codon usage chart in FIGS. 3A-B. A sequence is selected by choosing a codon for each of the amino acids of the polypeptide sequences. DNA molecules corresponding to each of the polypeptides can then by constructed by routine chemical synthesis methods. For example, shorter oligonucleotides can be synthesized, and then ligated in the appropriate relationships to construct the full-length coding sequences. 0161 The following sequences are provided in the sequence listing herein: interferon alpha amino acid sequence, SEQ ID NO:9; interferon alpha wild type nucleic acid sequence, SEQ ID NO:10; interferon alpha synthetic nucleic acid sequence with optimized codon usage, SEQ ID NO:11; interferon alpha nucleic acid sequence with additional/semi-optimized codon usage, SEQ ID NO:12; IL-12 p40 subunit amino acid sequence, SEQ ID NO:1; IL-12 p40 wild type nucleic acid sequence, SEQ ID NO:2; IL-12 p40 synthetic nucleic acid sequence with all codons optimized, SEQ ID NO:3; IL-12 p40 subunit nucleic acid sequence with all codons optimized except when same nucleic acids were too close/abundant, SEQ ID NO:4; IL-12 p35 amino acid sequence, SEQ ID NO:5; IL-12 p35 wild type nucleic acid sequence, SEQ ID NO:6; IL-12 p35 synthetic nucleic acid sequence with all codons optimized, SEQ ID NO:7; IL-12 p35 subunit nucleic acid sequence with all codons optimized except when same nucleic acids were too close/abundant, SEQ ID NO:8. Those skilled in the art will realize that various nucleic acid sequences with optimized codon usage can be constructed, for example based on the various combinations shown below, wherein optimal usage for each codon is shown below the IL-12 p35 and p40 subunit wild type sequences and the interferon alpha wild type sequence.

Sequences Encoding Human IL-12 p35 0162 First line: natural sequence (SEQ ID NO. 6) 0163 Second line: all codons optimized (SEQ ID NO. 7) 0164 Third line: all codons optimized except when same nucleic acids were too close/abundant (changes between second and third lines bolded) (SEQ ID NO. 8) 7ATG TGT CCA GCG CGC AGC CTC CTC CTT GTG GCT ACC CTG GTC CTC CTG GAC CAC CTC ACT ATG TGC CCC GCC CGC AGC CTG CTG CTG GTG GCC ACC CTG GTG CTG CTG GAC CAC CTG AGC ATG TGC CCC GCC CGC AGC CTG CTG CTC GTG GCC ACC CTG GTG CTC CTG GAC CAC CTC AGC TTG GCC AGA AAC CTC CCC GTG GCC ACT CCA GAC CCA GGA ATG TTC CCA TGC CTT CAC CAC CTG GCC CGC AAC CTG CCC GTG GCC ACC CCC GAC CCC GGC ATG TTC CCC TGC CTG CAC CAC CTG GCC CGC AAC CTC CCC GTG GCC ACC CCA GAC CCC GGC ATG TTC CCA TGC CTG CAC CAC TCC CAA AAC CTG CTG AGG GCC GTC AGC AAC ATG CTC CAG AAG GCC AGA CAA ACT CTA GAA AGC CAG AAC CTG CTG GCG GCC GTG AGC AAC ATG CTG CAG AAG GCC GCG CAG ACC CTG GAG AGC CAG AAC CTG CTG GCG GCC GTG AGC AAC ATG CTG CAG AAG GCC GCG CAG ACC CTG GAG TTT TAC CCT TGC ACT TCT GAA GAG ATT GAT CAT GAA GAT ATC ACA AAA GAT AAA ACC AGC TTC TAC CCC TGC ACC AGC GAG GAG ATC GAC CAC GAG GAC ATC ACC AAG GAC AAG ACC AGC TTC TAC CCC TGC ACC AGC GAG GAG ATC GAC CAC GAG GAC ATC ACC AAG GAC AAG ACC AGC ACA GTG GAG GCC TGT TTA CCA TTG GAA TTA ACC AAG AAT GAG AGT TGC CTA AAT TCC AGA ACC GTG GAG GCC TGC CTG CCC CTG GAG CTG ACC AAG AAC GAG AGC TGC CTG AAC AGC CGC ACC GTG GAG GCC TGC CTG CCC CTC GAG TTA ACC AAG AAC GAG AGC TGC CTC AAC AGC CGC GAG ACC TCT TTC ATA ACT AAT GGG AGT TGC CTG GCC TCC AGA AAG ACC TCT TTT ATG ATG GAG ACC AGC TTC ATC ACC AAC GGC AGC TGC CTG GCC AGC CGC AAG ACC AGC TTC ATG ATG GAG ACC TCC TTC ATC ACC AAC GGC ACT TGC CTG GCC TCC CGC AAG ACC AGC TTC ATG ATG GCC CTG TGC CTT AGT AGT ATT TAT GAA GAC TTG AAG ATG TAC CAG GTG GAG TTC AAG ACC GCC CTG TGC CTG AGC AGC ATC TAC GAG GAC CTG AAG ATG TAC CAG GTG GAG TTC AAG ACC GCC CTG TGC CTG AGC TCC ATC TAC GAG GAC CTG AAG ATG TAC CAG GTG GAG TTC AAG ACC ATG AAT GCA AAG CTT CTG ATG GAT CCT AAG AGG CAG ATC TTT CTA GAT CAA AAC ATG CTG ATG AAC GCC AAG CTG CTG ATG GAC CCC AAG CTC CAG ATC TTC CTG GAC CAG AAC ATG CTG ATG AAC GCC AAG CTC CTG ATG GAC CCC AAG CTC CAG ATC TTC CTG GAC CAG AAC ATG CTG GCA GTT ATT GAT GAG CTG ATG CAG GCC CTG AAT TTC AAC AGT GAG ACT GTG CCA CAA AAA GCC GTG ATC GAC GAG CTG ATG CAG GCC CTG AAC TTC AAC AGC GAG ACC GTG CCC CAG AAG GCC GTG ATC GAC GAG CTG ATG CAG GCC CTG AAC TTC AAC AGC GAG ACC GTG CCC CAG AAG TCC TCC CTT GAA GAA CCG GAT TTT TAT AAA ACT AAA ATC AAG CTC TGC ATA CTT CTT CAT AGC AGC CTG GAG GAG CCC GAC TTC TAC AAG ACC AAG ATC AAG CTG TGC ATC CTG CTG CAC AGC AGC CTG GAG GAG CCC GAC TTC TAC AAG ACC AAG ATC AAG CTG TGC ATC CTG CTG CAC GCT TTC AGA ATT CGG GCA GTG ACT ATT GAC AGA GTG ACG AGC TAT CTG AAT GCT TCC TAA GCC TTC CGC ATC CGC GCC GTG ACC ATC GAC CGC GTG ACC AGC TAC CTG AAC GCC ACC TGA GCC TTC CGC ATC CGG GCC GTG ACC ATC GAC CGC GTG ACC AGC TAC CTG AAC GCC ACG TGA

0165 Additional Optimized Sequences Coding For IL-12 p35 Subunit 0166 First line: SEQ.ID.NO.5 0167 Second line: SEQ.ID.NO.24 0168 Third line: SEQ.ID.NO.26 0169 Fourth line: SEQ.ID.NO.27 0170 Fifth line: SEQ.ID.NO.28 0171 Sixth line: SEQ.ID.NO.29 0172 Seventh line: SEQ.ID.NO.30 0173 Eighth line: SEQ.ID.NO.31 81020Met Cys Pro Ala Arg Ser Leu Leu Leu Val Ala Thr Leu Val Leu Leu Asp His Leu SerATG TGY CCN GCN MGN WSN YTN YTN YTN GTN GCN ACN YTN GTN YTN YTN GAY CAY YTN WSN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ATG TGT CCT GCT CGT TCT TTA TTA TTA GTT GCT ACT TTA GTT TTA TTA GAT CAT TTA TCTTGC CCC GCC CGC TCC TTG TTG TTG GTC GCC ACC TTG GTC TTG TTG GAC CAC TTG TCCCCA GCA CGA TCA CTT CTT CTT GTA GCA ACA CTT GTA CTT CTTCTT TCACCG GCG CGG TCG CTC CTC CTC GTG GCG ACG CTC GTG CTC CTCCTC TCGAGA AGT CTA CTA CTACTACTA CTACTA AGTAGG AGC CTG CTG CTGCTGCTG CTGCTG AGC 3040Leu Ala Arg Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His HisYTN GCN MGN AAY YTN CCN GTN GCN ACN CCN GAY CCN GGN ATG TTY CCN TGY YTN CAY CAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTA GCT CGT AAT TTA CCT GTT GCT ACT CCT GAT CCT GGT ATG TTT CCT TGT TTA CAT CATTTG GCC CGC AAC TTG CCC GTC GCC ACC CCC GAC CCC GGCTTC CCC TGC TTG CAC CACCTT GCA CGACTT CCA GTA GCA ACA CCACCA GGACCACTTCTC GCG CGGCTC CCG GTG GCG ACG CCGCCG GGGCCGCTCCTAAGACTACTACTGAGGCTGCTG 5060Ser Gln Asn Leu Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu GluWSN CAA AAY YTN YTN MGN GCN GTN WSN AAY ATG YTN CAA AAA GCN MGN CAA ACN YTN GAA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TCT CAA AAT TTA TTA CGT GCT GTT TCT AAT ATG TTA CAA AAA GCT CGT CAA ACT TTA GAATCC CAG AAC TTG TTG CGC GCC GTC TCC AACTTG CAG AAG GCC CGC CAG ACC TTG GAGTCACTT CTT CGA GCA GTA TCACTTGCA CGAACA CTTTCGCTC CTC CGG GCG GTG TCGCTCGCG CGGACG CTCAGTCTA CTA AGAAGTCTAAGACTAAGCCTG CTG AGGAGCCTGAGGCTG 7080Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp Lys Thr SerTTY TAY CCN TGY ACN WSN GAA GAA ATH GAY CAY GAA GAY ATH ACN AAA GAY AAA ACN WSN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTT TAT CCT TGT ACT TCT GAA GAA ATT GAT CAT GAA GAT ATT ACT AAA GAT AAA ACT TCTTTC TAC CCC TGC ACC TCC GAG GAG ATC GAC CAC GAG GAC ATC ACC AAG GAC AAG ACC TCCCCAACA TCAATAATA ACAACA TCACCGACG TCGACGACG TCGAGTAGTAGCAGC 90100Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn Giu Ser Cys Leu Asn Ser ArgACN GTN GAA GCN TGY YTN CCN YTN GAA YTN ACN AAA AAY GAA WSN TGY YTN AAY WSN MGN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ACT GTT GAA GCT TGT TTA CCT TTA GAA TTA ACT AAA AAT GAA TCT TGT TTA AAT TCT CGTACC GTC GAG GCC TGC TTG CCC TTG GAG TTG ACC AAG AAC GAG TCC TGC TTG AAC TCC CGCACA GTAGCACTT CCA CTTCTT ACATCACTTTCA CGAACG GTGGCGCTC CCG CTCCTC ACGTCGCTCTCG CGGCTACTACTAAGTCTAAGT AGACTGCTGCTGAGCCTGAGC AGG 110120Glu Thr Ser Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met MetGAA ACN WSN TTY ATH ACN AAY GGN WSN TGY YTN GCN WSN MGN AAA ACN WSN TTY ATG ATG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GAA ACT TCT TTT ATT ACT AAT GGT TCT TGT TTA GCT TCT CGT AAA ACT TCT TTT ATG ATGGAG ACC TCC TTC ATC ACC AAC GGC TCC TGC TTG GCC TCC CGC AAG ACC TCC TTCACA TCAATA ACAGGA TCACTT GCA TCA CGAACA TCAACG TCGACGGGG TCGCTC GCG TCG CGGACG TCGAGTAGTCTAAGT AGAAGTAGCAGCCTGAGC AGGAGC 130140Ala Leu Cys Leu Ser Ser lie Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys ThrGCN YTN TGY YTN WSN WSN ATE TAY GAA GAY YTN AAA ATG TAY CAA GTN GAA TTY AAA ACN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT TTA TGT TTA TCT TCT ATT TAT GAA GAT TTA AAA ATG TAT CAA GTT GAA TTT AAA ACTGCC TTG TGC TTG TCC TCC ATC TAC GAG GAC TTG AAGTAC CAG GTC GAG TTC AAG ACCGCA CTTCTT TCA TCA ATACTTGTAACAGCG CTCCTC TCG TCGCTCGTGACGCTACTA AGT AGTCTACTGCTG AGC AGCCTG 150160Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln Asn Met LeuATG AAY GCN AAA YTN YTN ATG GAY CCN AAA MGN CAA ATE TTY YTN GAY CAA AAY ATG YTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ATG AAT GCT AAA TTA TTA ATG GAT CCT AAA CGT CAA ATT TTT TTA GAT CAA AAT ATG TTAAAC GCC AAG TTG TTGGAC CCC AAG CGC CAG ATC TTC TTG GAC CAG AACTTGGCACTT CTTCCACGAATACTTCTTGCGCTC CTCCCGCGGCTCCTCCTA CTAAGACTACTACTG CTGAGGCTGCTG 170180Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro Gln LysGCN GTN ATE GAY GAA YTN ATG CAA GCN YTN AAY TTY AAY WSN GAA ACN GTN CCN CAA AAA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT GTT ATT GAT GAA TTA ATG CAA GCT TTA AAT TTT AAT TCT GAA ACT GTT CCT CAA AAAGCC GTC ATC GAC GAG TTGCAG GCC TTG AAC TTC AAC TCC GAG ACC GTC CCC CAG AAGGCA GTA ATACTTGCA CTTTCAACA GTA CCAGCG GTGCTCGCG CTCTCGACG GTG CCGCTACTAAGTCTGCTGAGC 190200Ser Ser Leu Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu HisWSN WSN YTN GAR GAR CCN GAY TTY TAY AAR ACN AAR ATH AAR YTN TGY ATH YTN YTN CAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TCT TCT TTA GAA GAA CCT GAT TTT TAT AAA ACT AAA ATT AAA TTA TGT ATT TTA TTA CATTCC TCC TTG GAG GAG CCC GAC TTC TAC AAG ACC AAG ATC AAG TTG TGC ATC TTG TTG CACTCA TCA CTTCCAACAATACTTATA CTT CTTTCG TCG CTCCCGACGCTCCTC CTCAGT AGT CTACTACTA CTAAGC AGC CTGCTGCTG CTG 210220Ala Phe Arg lie Arg Ala Val Thr Ile Asp Arg Val Thr Ser Tyr Leu Asn Ala Ser ***GCN TTY MGN ATH MGN GCN GTN ACN ATH GAY MGN GTN ACN WSN TAY YTN AAY GCN WSN TAA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT TTT CGT ATT CGT GCT GTT ACT ATT GAT CGT GTT ACT TCT TAT TTA AAT GCT TCT TAAGCC TTC CGC ATC CGC GCC GTC ACC ATC GAC CGC GTC ACC TCC TAC TTG AAC GCC TCC TAGGCACGA ATA CGA GCA GTA ACA ATACGA GTA ACA TCACTTGCA TCA TGAGCGCGGCGG GCG GTG ACGCGG GTG ACG TCGCTCGCG TCGAGAAGAAGAAGTCTAAGTAGGAGGAGGAGCCTGAGC

Sequences Encoding Human IL-12 p40 0174 First line: natural sequence (SEQ ID NO. 2) 0175 Second line: all codons optimized (SEQ ID NO. 3) 0176 Third line: all codons optimized except when same nucleic acids were too close/abundant (changes between second and third lines bolded) (SEQ ID NO. 4) 9ATG TGT CAC CAG CAG TTG GTC ATC TCT TGG TTT TCC CTG GTT TTT CTG GCA TCT CCC CTCATG TGC CAC CAG CAG CTG GTG ATC AGC TGG TTC AGC CTG GTG TTC CTG GCC AGC CCC CTGATG TGC CAC CAG CAG CTG GTG ATC AGC TGG TTC TCC CTG GTG TTT CTG GCC AGC CCC CTC GTG GCC ATA TGG GAA CTG AAG AAA GAT GTT TAT GTC GTA GAA TTG GAT TGG TAT CCG GATGTG GCC ATC TGG GAG CTG AAG AAG GAC GTG TAC GTG GTG GAG CTG GAC TGG TAC CCC GACGTG GCC ATC TGG GAG CTG AAG AAA GAC GTG TAC GTG GTC GAG CTG GAC TGG TAC CCC GAC GCC CCT GGA GAA ATG GTG GTC CTC ACC TGT GAC ACC CCT GAA GAA GAT GGT ATC ACC TGGGCC CCC GGC GAG ATG GTG GTG CTG ACC TGC GAC ACC CCC GAG GAG GAC GGC ATC ACC TGGGCC CCC GGC GAG ATG GTG GTC CTG ACC TGC GAC ACC CCC GAG GAA GAC GGC ATC ACC TGG ACC TTG GAC CAG AGC AGT GAG GTC TTA GGC TCT GGC AAA ACC CTG ACC ATC CAA GTC AAAACC CTG GAC CAG AGC AGC GAG GTG CTG GGC AGC GGC AAG ACC CTG ACC ATC CAG GTG AAGACC CTG GAC CAG AGC AGT GAG GTG CTG GGC TCC GGC AAG ACC CTG ACC ATC CAG GTG AAG GAG TTT GGA GAT GCT GGC CAG TAC ACC TGT CAC AAA GGA GGC GAG GTT CTA AGC CAT TCGGAG TTC GGC GAC GCC GGC CAG TAC ACC TGC CAC AAG GGC GGC GAG GTG CTG AGC CAC AGCGAG TTC GGC GAC GCC GGC CAG TAC ACC TGC CAC AAG GGA GGC GAG GTG CTG AGC CAC TCC CTC CTG CTG CTT CAC AAA AAG GAA GAT GGA ATT TGG TCC ACT GAT ATT TTA AAG GAC CAGCTG CTG CTG CTG CAC AAG AAG GAG GAC GGC ATC TGG AGC ACC GAC ATC CTG AAG GAC CAGCTC CTG CTG CTC CAC AAA AAG GAG GAC GGC ATC TGG AGC ACC GAC ATC CTG AAG GAC CAG AAA GAA CCC AAA AAT AAG ACC TTT CTA AGA TGC GAG GCC AAG AAT TAT TCT GGA CGT TTCAAG GAG CCC AAG AAC AAG ACC TTC CTG CGC TGC GAG GCC AAG AAC TAC AGC GGC CGC TTCAAG GAG CCC AAG AAC AAG ACC TTC CTG CGC TGC GAG GCC AAG AAC TAC AGC GGC CGC TTC ACC TGC TGG TGG CTG ACG ACA ATC AGT ACT GAT TTG ACA TTC AGT GTC AAA AGC AGC AGAACC TGC TGG TGG CTG ACC ACC ATC AGC ACC GAC CTG ACC TTC AGC GTG AAG AGC AGC AGGACC TGC TGG TGG CTG ACC ACG ATC AGC ACC GAC CTG ACC TTC AGT GTG AAG AGC AGC AGG GGC TCT TCT GAC CCC CAA GGG GTG ACG TGC GGA GCT GCT ACA CTC TCT GCA GAG AGA GTCGGC AGC AGC GAC CCC CAG GGC GTG ACC TGC GGC CCC GCC ACC CTG AGC GCC GAG CGC GTGGGC TCC AGC GAC CCC CAG GGC GTG ACC TGC GGC GCT GCC ACC CTG AGC GCC GAG CGC GTG AGA GGG GAC AAC AAG GAG TAT GAG TAC TCA GTG GAG TOC CAG GAG GAC AGT GCC TGC CCACGC GGC GAC AAC AAG GAG TAC GAG TAC AGC GTG GAG TGC CAG GAG GAC AGC GCC TGC CCCCGC GGC GAC AAC AAG GAG TAC GAG TAC AGC GTG GAG TGC CAG GAA GAC TCC GCC TGC CCC GCT GCT GAG GAG AGT CTG CCC ATT GAG GTC ATG GTG GAT GCC GTT CAC AAG CTC AAG TATGCC GCC GAG GAG AGC CTG CCC ATC GAG GTG ATG GTG GAC GCC GTC CAC AAG CTG AAG TACGCC GCT GAG GAG AGC CTG CCC ATC GAG GTG ATG GTG GAC GCC GTT CAC AAG CTG AAG TAC GAA AAC TAC ACC AGC AGC TTC TTC ATC AGG GAC ATC ATC AAA CCT GAC CCA CCC AAG AACGAG AAC TAC ACC AGC AGC TTC TTC ATC CGC GAC ATC ATC AAG CCC GAC CCC CCC AAG AACGAG AAC TAC ACC AGC AGC TTC TTC ATC CGC GAC ATC ATC AAG CCT GAC CCA CCC AAG AAC TTG CAG CTG AAG CCA TTA AAG AAT TCT CGG CAG GTG GAG GTC AGC TGG GAG TAC CCT GACCTG CAG CTG AAG CCC CTG AAG AAC AGC CGC CAG GTG GAG GTG AGC TGG GAG TAC CCC GACCTC CAG CTG AAG CCC CTC AAG AAC TCC CGC CAG GTG GAG GTG AGC TGG GAG TAC CCC GAC ACC TGG AGT ACT CCA CAT TCC TAC TTC TCC CTG ACA TTC TGC GTT CAG GTC CAG GGC AAGACC TGG AGC ACC CCC CAC AGC TAC TTC AGC CTG ACC TTC TGC GTG CAG GTG CAG GGC AAGACC TGG AGC ACG CCC CAC TCC TAC TTC TCC CTG ACC TTC TGC GTG CAG GTC CAG GGC AAG AGC AAG AGA GAA AAG AAA GAT AGA GTC TTC ACG GAC AAG ACC TCA GCC ACG GTC ATC TGCAGC AAG CGC GAG AAG AAG GAC CGC GTG TTC ACC GAC AAG ACC AGC GCC ACC GTG ATC TGCAGC AAG CGC GAG AAG AAA GAC COG GTG TTC ACC GAC AAG ACC AGC GCC ACC GTC ATC TGC CGC AAA AAT GCC AGC ATT AGC GTG CGG GCC CAG GAC CGC TAC TAT AGC TCA TCT TGG AGCCGC AAG AAC GCC AGC ATC AGC GTG CGC GCC CAG GAC CGC TAC TAC AGC AGC AGC TGG AGCCGC AAG AAC GCC AGC ATC AGC GTG CGC CCC CAG GAC CGC TAC TAT AGC TCC TCT TGG AGC GAA TGG GCA TCT GTG CCC TGC AGT TAGGAG TGG GCC AGC GTG CCC TGC AGC TAGGAG TGG GCC AGC GTG CCC TGC TCCTAG

Additional Optimized Sequences Coding For IL-12 p40 Subunit 0177 First line: SEQ.ID.NO.1 0178 Second line: SEQ.ID.NO.25 0179 Third line: SEQ.ID.NO.32 0180 Fourth line: SEQ.ID.NO.33 0181 Fifth line: SEQ.ID.NO.34 0182 Sixth line: SEQ.ID.NO.35 0183 Seventh line: SEQ.ID.NO.36 0184 Eighth line: SEQ.ID.NO.37 101020Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu Ala Ser Pro LeuATG TGY CAY CAA CAA YTN GTN ATH WSN TGG TTY WSN YTN GTN TTY YTN GCN WSN CCN YTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ATG TGT CAT CAA CAA TTA GTT ATT TCT TGG TTT TCT TTA GTT TTT TTA GCT TCT CCT TTATGC CAC CAG CAG TTG GTC ATC TCCTTC TCC TTG GTC TTC TTG GCC TCC CCC TTGCTT GTA ATA TCATCA CTT GTACTT GCA TCA CCA CTTCTC GTGTCGTCG CTC GTGCTC GCG TCG CCG CTCCTAAGTAGT CTACTAAGTCTACTGAGCAGC CTGCTGAGCCTG 3040Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val Val Glu Leu Asp Trp Tyr Pro AspGTN GCN ATH TGG GAA YTN AAA AAA GAY GTN TAY GTN GTH GAA YTN GAY TGG TAY CCN GAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GTT GCT ATT TGG GAA TTA AAA AAA GAT GTT TAT GTT GTT GAA TTA GAT TGG TAT CCT GATGTC GCC ATCGAG TTG AAG AAG GAC GTC TAC GTC GTC GAG TTG GACTAC CCC GACGTA GCA ATACTTGTAGTA GTACTTCCAGTG GCGCTCGTGGTG GTGCTCCCGCTACTACTGCTG 5060Ala Pro Gly Glu Met Val Val Leu Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr TrpGCN CCH GGN GAA ATG GTN GTN YTN ACH TGY GAY ACN CCN GAA GAA GAY GGN ATH ACN TGG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT CCT GGT GAA ATG GTT GTT TTA ACT TGT GAT ACT CCT GAA GAA GAT GGT ATT ACT TGGGCC CCC GGC GAGGTC GTC TTG ACC TGC GAC ACC CCC GAG GAG GAC GGC ATC ACCGCA CCA GGAGTA GTA CTT ACAACA CCAGGA ATA ACAGCG CCG GGGGTG GTG CTC ACGACG CCGGGGACGCTACTG 7080Thr Leu Asp Gln Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val LysACN YTN GAY CAR WSN WSN GAR GTN YTN GGN WSN GGH AAR ACN YTN ACN ATH CAA GTN AAR--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ACT TTA GAT CAA TCT TCT GAA GTT TTA GGT TCT GGT AAA ACT TTA ACT ATT CAA GTT AAAACC TTG GAC CAG TCC TCC GAG GTC TTG GGC TCC GGC AAG ACC TTG ACC ATC CAG GTC AAGACA CTTTCA TCAGTA CTT GGA TCA GGAACA CTT ACA ATAGTAACG CTCTCG TCGGTG CTC GGG TCG GGGACG CTC ACGGTGCTAAGT AGTCTAAGTCTACTGAGC AGCCTGAGCCTG 90100Glu Phe Gly Asp Ala Gly Gln TYr Thr Cys His Lys Gly Gly Glu Val Leu Ser His SerGAR TTY GGN GAY GCN GGN CAR TAY ACN TGY CAY AAR GGN GGN GAR GTN YTN WSN CAY WSN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GAA TTT GGT GAT GCT GGT CAA TAT ACT TGT CAT AAA GGT GGT GAA GTT TTA TCT CAT TCTGAG TTC GGC GAC GCC GGC CAG TAC ACC TGC CAC AAG GGC GGC GAG GTC TTG TCC CAC TCCGGAGCA GGAACAGGA GGAGTA CTT TCGTCGGGGGCG GGGACGGGG GGGGTG CTC TCGAGTCTA AGTAGTCTG AGCAGC 110120Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp Ser Thr Asp Ile Leu Lys Asp GlnYTN YTN YTN YTN CAY AAR AAR GAR GAY GGN ATH TGG WSN ACN GAY ATH YTN AAR GAY CAR--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTA TTA TTA TTA CAT AAA AAA GAA GAT GGT ATT TGG TCT ACT GAT ATT TTA AAA GAT CAATTG TTG TTG TTG CAC AAG AAG GAG GAC GGC ATCTCC ACC GAC ATC TTG AAG GAC CAGCTT CTT CTT CTTGGA ATATCA ACAATA CTTCTC CTC CTC CTCGGGTCG ACGCTCCTA CTA CTA CTAAGTCTACTG CTG CTG CTGAGCCTG 130140Lys Glu Pro Lys Asn Lys Thr Phe Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg PheAAR GAR CCN AAR AAY AAR ACN TTY YTN MGN TGY GAR GCN AAR AAY TAY WSN GGN MGN TTY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---AAA GAA CCT AAA AAT AAA ACT TTT TTA CGT TGT GAA GCT AAA AAT TAT TCT GGT CGT TTTAAG GAG CCC AAG AAC AAG ACC TTC TTG CGC TGC GAG GCC AAG AAC TAC TCC GGC CGC TTCCCAACACTT CGAGCATCA GGA CGACCGACGCTC CGGGCGTCG GGG CGGCTA AGAAGTAGACTG AGGAGCAGG 150160Thr Cys Trp Trp Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser ArgACN TGY TGG TGG YTN ACN ACN ATH WSW ACN GAY YTN ACN TTY WSN GTN AAR WSN WSN MGN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ACT TGT TGG TGG TTA ACT ACT ATT TCT ACT GAT TTA ACT TTT TCT GTT AAA TCT TCT CGTACC TGCTTG ACC ACC ATC TCC ACC GAC TTG ACC TTC TCC GTC AAG TCC TCC CGCACACTT ACA ACA ATA TCA ACACTT ACATCA GTATCA TCA CGAACGCTC ACG ACGTCG ACGCTC ACGTCG GTGTCG TCG CGGCTAAGTCTAAGTAGT AGT AGACTGAGCCTGAGCAGC AGC AGG 170180Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser Ala Glu Arg ValGGN WSN WSN GAY CCN CAR GGN GTN ACN TGY GGN GCN GCN ACN YTN WSW GCN GAR MGN GTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GGT TCT TCT GAT CCT CAA GGT GTT ACT TGT GGT GCT GCT ACT TTA TCT GCT GAA CGT GTTGGC TCC TCC GAC CCC CAG GGC GTC ACC TGC GGC GCC GCC ACC TTG TCC GCC GAG CGC GTCGGA TCA TCACCAGGA GTA ACAGGA GCA GCA ACA CTT TCA GCACGA GTAGGG TCG TCGCCGGGG GTG ACGGGG GCG GCG ACG CTC TCG GCGCGG GTGAGT AGTCTA AGTAGAAGC AGCCTG AGCAGG 190200Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu Cys Gln Glu Asp Ser Ala Cys ProMGN GGN GAY AAY AAA GAA TAY GAA TAY WSN GTN GAA TGY CAA GAA GAY WSN GCN TGY CCN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---CGT GGT GAT AAT AAA GAA TAT GAA TAT TCT GTT GAA TGT CAA GAA GAT TCT GCT TGT CCTCGC GGC GAC AAC AAG GAG TAC GAG TAC TCC GTC GAG TGC CAG GAG GAC TCC GCC TGC CCCCGA GGATCA GTATCA GCACCACGG GGGTCG GTGTCG GCGCCGAGAAGTAGTAGGAGCAGC 210220Ala Ala Glu Glu Ser Leu Pro Ile Glu Val Met Val Asp Ala Val His Lys Leu Lys TyrGCN GCN GAA GAA WSN YTN CCN ATH GAA GTN ATG GTN GAY GCN GTN CAY AAA YTN AAA TAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT GCT GAA GAA TCT TTA CCT ATT GAA GTT ATG GTT GAT GCT GTT CAT AAA TTA AAA TATGCC GCC GAG GAG TCC TTG CCC ATC GAG GTCGTC GAC GCC GTC CAC AAG TTG AAG TACGCA GCATCA CTT CCA ATAGTAGTAGCA GTACTTGCG GCGTCG CTC CCGGTGGTGGCG GTGCTCAGT CTACTAAGC CTGCTG 230240Glu Asn Tyr Thr Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Lys AsnGAR AAY TAY ACN WSN WSN TTY TTY ATH MGN GAY ATH ATH AAA CCN GAY CCN CCN AAR AAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GAA AAT TAT ACT TCT TCT TTT TTT ATT CGT GAT ATT ATT AAA CCT GAT CCT CCT AAA AATGAG AAC TAC ACC TCC TCC TTC TTC ATC CGC GAC ATC ATC AAG CCC GAC CCC CCC AAG AACACA TCA TCAATA CGAATA ATACCACCA CCAACG TCG TCGCGGCCGCCG CCGAGT AGTAGAAGC AGCAGG 250260Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp Glu Tyr Pro AspYTN CAA YTN AAA CCN YTN AAA AAY WSN MGN CAA GTN GAA GTN WSN TGG GAA TAY CCN GAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTA CAA TTA AAA CCT TTA AAA AAT TCT CGT CAA GTT GAA GTT TCT TGG GAA TAT CCT GATTTG CAG TTG AAG CCC TTG AAG AAC TCC CCC CAG GTC GAG GTC TCCGAG TAC CCC GACCTTCTTCCA CTTTCA CGAGTAGTA TCACCACTCCTCCCG CTCTCG CGGGTGGTG TCGCCGCTACTACTAAGT AGAAGTCTGCTGCTGAGC AGGAGC 270280Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr Phe Cys Val Gln Val Gln Gly LysACN TGG WSN ACN CCN CAY WSN TAY TTY WSN YTN ACN TTY TGY GTN CAA GTN CAA GGN AAA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ACT TGG TCT ACT CCT CAT TCT TAT TTT TCT TTA ACT TTT TGT GTT CAA GTT CAA GCT AAAACCTCC ACC CCC CAC TCC TAC TTC TCC TTG ACC TTC TGC GTC CAG GTC CAG GGC AAGACATCA ACA CCATCATCA CTT ACAGTAGTAGGAACGTCG ACG CCGTCGTCG CTC ACGGTGGTGGGGAGTAGTAGT CTAAGCAGCAGC CTG 290300Ser Lys Arg Glu Lys Lys Asp Arg Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile CysWSN AAR MGN GAA AAA AAA GAY MGN GTN TTY ACN GAY AAA ACN WSN GCN ACN GTN ATH TGY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TCT AAA CGT GAA AAA AAA GAT CGT GTT TTT ACT GAT AAA ACT TCT GCT ACT GTT ATT TGTTCC AAG CGC GAG AAG AAG GAC CGC GTC TTC ACC GAC AAG ACC TCC GCC ACC GTC ATC TGCTCACGACGA GTAACAACA TCA GCA ACA GTA ATATCGCGGCGG GTGACGACG TCG GCG ACG GTGAGTAGAAGAAGTAGCAGGAGGAGC 310320Arg Lys Asn Ala Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp SerMGN AAR AAY GCN WSN ATE WSN GTN MGN GCN CAA GAY MGN TAY TAY WSN WSN WSN TGG WSN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---CGT AAA AAT GCT TCT ATT TCT GTT CGT GCT CAA GAT CGT TAT TAT TCT TCT TCT TGG TCTCGC AAG AAC GCC TCC ATC TCC GTC CGC GCC CAG GAC CGC TAC TAC TCC TCC TCCTCCCGAGCA TCA ATA TCA GTA CGA GCACGATCA TCA TCATCACGGGCG TCGTCG GTG CGG GCGCGGTCG TCG TCGTCGAGAAGTAGTAGAAGAAGT AGT AGTAGTAGGAGCAGCAGGAGGAGC AGC AGCAGC Glu Trp Ala Ser Val Pro Cys Ser ***GAR TGG GCN WSN GTN CCN TGY WSN TRR--- --- --- --- --- --- --- --- ---GAA TGG GCT TCT GTT CCT TGT TCT TAAGAGGCC TCC GTC CCC TGC TCC TAGGCA TCA GTA CCATCA TGAGCG TCG GTG CCGTCGAGTAGTAGCAGC

Wild Type Sequence Coding for Interferon Alpha 0185

11918273645545ATG GCC TTG ACC TTT GCT TTA CTG GTG GCC CTC CTG GTG CTC AGC TGC AAG TCA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---MALTFALLVALLVLSCKS 6372819099108AGC TGC TCT GTG GGC TGT GAT CTG CCT CAA ACC CAC AGC CTG GGT AGC AGG AGG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---SCSVGCDLPQTHSLGSRR 117126135144153162ACC TTG ATG CTC CTG GCA CAG ATG AGG AGA ATC TCT CTT TTC TCC TGC TTG AAG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TLMLLAQMRRISLFSCLK 171180189198207216GAC AGA CAT GAC TTT GGA TTT CCC CAG GAG GAG TTT GGC AAC CAG TTC CAA AAG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---DRHDFGFPQEEFGNQFQK 225234243252261270GCT GAA ACC ATC CCT GTC CTC CAT GAG ATG ATC CAG CAG ATC TTC AAT CTC TTC--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---AETIPVLHEMIQQIFNLF 279288297306315324AGC ACA AAG GAC TCA TCT GCT GCT TGG GAT GAG ACC CTC CTA GAC AAA TTC TAC--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---STKDSSAAWDETLLDKFY 333342351360369378ACT GAA CTC TAC CAG CAG CTG AAT GAC CTG GAA GCC TGT GTG ATA CAG GGG GTG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TELYQQLNDLEACVIQGV 387396405414423432GGG GTG ACA GAG ACT CCC CTG ATG AAG GAG GAC TCC ATT CTG GCT GTG AGG AAA--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GVTETPLMKEDSILAVAK 441450459468477486TAC TTC CAA AGA ATC ACT CTC TAT CTG AAA GAG AAG AAA TAC AGC CCT TGT GCC--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---YFQRITLYLKEKKYSPCA 495504513522531540TGG GAG GTT GTC AGA GCA GAA ATC ATG AGA TCT TTT TCT TTG TCA ACA AAC TTG--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---WEVVRAEIMRSFSLSTNL 549558567CAA GAA AGT TTA AGA AGT AAG GAA TGA 3--- --- --- --- --- --- --- --- ---QESLRSKE*

Interferon Alpha Coding Sequence with all Codons Optimized (SEQ ID NO:11) 0186

12ATG GCC CTG ACC TTC GCC CTG CTG GTG GCC CTG CTG GTG CTG AGC TGC AAG AGC AGC TGC TCC GTG GOG TGC GAC CTG CCC CAG ACC CAC AGC CTG GGG AGC CGG CGG ACC CTG ATG CTG CTG GCC CAG ATG CGG CGG ATC AGC CTG TTC AGC TGC CTG AAG GAC CGG CAC GAC TTC GGG TTC CCC CAG GAG GAG TTC GGG AAC CAG TTC CAG AAG GCC GAG ACC ATC CCC GTG CTG CAC GAG ATG ATC CAG CAG ATC TTC AAC CTG TTC AGC ACC AAG GAC AGC AGC GCC GCC TGG GAC GAG ACC CTG CTG GAC AAG TTC TAC ACC GAG CTG TAC CAG CAG CTG AAC GAC CTG GAG GCC TGC GTG ATC CAG GGG GTG GGG GTG ACC GAG ACC CCC CTG ATG AAG GAG GAC AGC ATC CTG GCC GTG CGG AAG TAC TTC CAG CGG ATC ACC CTG TAC CTG AAG GAG AAG AAG TAC TCC CCC TGC GCC TGG GAG GTG GTG CGG GCC GAG ATC ATG CGG AGC TTC AGC CTG AGC ACC AAC CTG CAG GAG AGC CTG CGG AGC AAG GAG TGA

Additional/Semi Optimized Sequence Coding for Interferon Alpha 0187 First line: SEQ.ID.NO.9 0188 Second line: SEQ.ID.NO.12 0189 Third line: SEQ.ID.NO.38 0190 Fourth line: SEQ.ID.NO.39 0191 Fifth line: SEQ.ID.NO.40 0192 Sixth line: SEQ.ID.NO.41 0193 Seventh line: SEQ.ID.NO.42 0194 Eighth line: SEQ.ID.NO.43 131020MET ALA LEU THR PHE ALA LEU LEU VAL ALA LEU LEU VAL LEU SER CYS LYS SER SER CYSATG GCN YTN ACN TTY GCN YTN YTN GTN GCN YTN YTN GTN YTN WSN TGY AAR WSN WSN TGY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---ATC GCT TTA ACT TTT GCT TTA TTA GTT GCT TTA TTA GTT TTA TCT TGT AAA TCT TCT TGTGCC TTG ACC TTC GCC TTG TTG GTC GCC TTG TTG GTC TTG TCC TGC AAG TCC TCC TGCGCA CTT ACAGCA CTT CTT GTA GCA CTT CTT GTA CTT TCATCA TCAGCG CTC ACGGCG CTC CTC GTG GCG CTC CTC GTG CTC TCGAGT AGTCTACTA CTACTA CTACTA AGTAGT AGTCTGCTG CTGCTG CTGCTG AGCAGC AGC 3040SER VAL GLY CYS ASP LEU PRO GLN THR HIS SER LEU GLY SER ARG ARG THR LEU MET LEUWSN GTN GGN TGY GAY YTN CCN CAR ACN CAY WSN YTN GGN WSN MGN MGN ACN YTN ATG YTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TCT GTT GGT TGT GAT TTA CCT CAA ACT CAT TCT TTA GGT TCT CGT CGT ACT TTA ATG TTATCC GTC GGC TGC GAC TTG CCC CAG ACC CAC TCC TTG GGC TCC CGC CGC ACC TTGTTGTCA GTA GGACTT CCAACATCA CTT GGA TCA CGA CGA ACA CTTCTTTCG GTG GGGCTC CCGACGTCG CTC GGG TCG CGG CGG ACG CTCCTCAGTCTAAGT CTAAGT AGA AGACTACTAAGCCTGAGC CTGAGC AGG AGGCTGCTG 5060LEU ALA GLN MET ARG ARG ILE SER LEU PHE SER CYS LEU LYS ASP ARG HIS ASP PHE GLYYTN GCN CAR ATG MGN MGN ATH WSN YTN TTY WSN TGY YTN AAR GAY MGN CAY GAY TTY GGN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTA GCT CAA ATG CGT CGT ATT TCT TTA TTT TCT TGT TTA AAA GAT CGT CAT GAT TTT GGTTTG GCC CAGCGC CGC ATC TCC TTG TTC TCC TGC TTG AAG GAC CGC CAC GAC TTC GGCCTT GCACGA CGA ATA TCA CTTTCACTTCGAGGACTC GCGCGG CGGTCG CTCTCGCTCCGGGGGCTAAGA AGAAGT CTAAGTCTAAGACTGAGG AGGAGC CTGAGCCTGAGG 7080PHE PRO GLN GLU GLU PHE GLY ASN GLN PHE GLN LYS ALA GLU THR ILE PRO VAL LEU HISTTY CCN CAR GAR GAR TTY GGN AAY CAR TTY CAR AAR GCN GAR ACN ATH CCN GTN YTN CAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TTT CCT CAA GAA GAA TTT GGT AAT CAA TTT CAA AAA GCT GAA ACT ATT CCT GTT TTA CATTTC CCC CAG GAG GAG TTC GGC AAC CAG TTC CAG AAG GCC GAG ACC ATC CCC GTC TTG CACCCAGGAGCAACA ATA CCA GTA CTTCCGGGGGCGACGCCG GTG CTCCTACTG 90100GLU MET ILE GLN GLN ILE PHE ASN LEU PHE SER THR LYS ASP SER SER ALA ALA TRP ASPGAR ATG ATH CAR CAR ATH TTY AAY YTN TTY WSN ACN AAR GAY WSN WSN GCN GCN TGG GAY--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GAA ATG ATT CAA CAA ATT TTT AAT TTA TTT TCT ACT AAA GAT TCT TCT GCT GCT TGG GATGAGATC CAG CAG ATC TTC AAC TTG TTC TCC ACC AAG GAC TCC TCC GCC GCCGACATAATACTTTCA ACATCA TCA GCA GCACTCTCG ACGTCG TCG GCG GCGCTAAGTAGT AGTCTGAGCAGC AGC 110120GLU THR LEU LEU ASP LYS PHE TYR THR GLU LEU TYR GLN GLN LEU ASN ASP LEU GLU ALAGAR ACN YTN YTN GAY AAR TTY TAY ACN GAR YTN TAY CAR CAR YTN AAY GAY YTN GAR GCN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GAA ACT TTA TTA GAT AAA TTT TAT ACT GAA TTA TAT CAA CAA TTA AAT GAT TTA GAA GCTGAG ACC TTG TTG GAC AAG TTC TAC ACC GAG TTG TAC CAG CAG TTG AAC GAC TTG GAG GCCACA CTT CTTACACTTCTTCTTGCAACG CTC CTCACGCTCCTCCTCGCGCTA CTACTACTACTACTGCTG CTGCTGCTGCTG 130140CYS VAL ILE GLN GLY VAL GLY VAL THR GLU THR PRO LEU MET LYS GLU ASP SER ILE LEUTGY GTN ATH CAR GGN GTN GGN GTN ACN GAR ACN CCN YTN ATG AAR GAR GAY WSN ATH YTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TGT GTT ATT CAA GGT GTT GGT GTT ACT GAA ACT CCT TTA ATG AAA GAA GAT TCT ATT TTATGC GTC ATC CAG GGC GTC GGC GTC ACC GAG ACC CCC TTGAAG GAG GAC TCC ATC TTGGTA ATAGGA GTA GGA GTA ACAACA CCA CTTTCA ATA CTTGTGGGG GTG GGG GTG ACGACG CCG CTCTCGCTCCTAAGTCTACTGAGCCTG 150160ALA VAL ARG LYS TYR PHE GLN ARG ILE THR LUE TYR LEU LYS GLU LYS LYS TYR SER PROGCN GTN MGN AAR TAY TTY CAR MGN ATH ACN YTN TAY YTN AAR GAR AAR AAR TAY WSN CCN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---GCT GTT CGT AAA TAT TTT CAA CGT ATT ACT TTA TAT TTA AAA GAA AAA AAA TAT TCT CCTGCC GTC CGC AAG TAC TTC CAG CGC ATC ACC TTG TAC TTG AAG GAG AAG AAG TAC TCC CCCGCA GTA CGACGA ATA ACA CTTCTTTCA CCAGCG GTG CGGCGGACG CTCCTCTCG CCGAGAAGACTACTAAGTAGGAGGCTGCTGAGC 170180CYS ALA TRP GLU VAL VAL ARG ALA GLU ILE MET ARG SER PHE SER LEU SER THR ASN LEUTGY GCN TGG GAR GTN GTN MGN GCN GAR ATH ATG MGN WSN TTY WSN YTN WSN ACN AAY YTN--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---TGT GCT TGG GAA GTT GTT CGT GCT GAA ATT ATG CGT TCT TTT TCT TTA TCT ACT ATT TTATGC GCCGAG GTC GTC CGC GCC GAG ATCCGC TCC TTC TCC TTG TCC ACC AAC TTGGCAGTA GTA CGA GCAATACGA TCATCA CTT TCA ACACTTGCGGTG GTG CGG GCGCGG TCGTCG CTC TCG ACGCTCAGAAGA AGTAGT CTA AGTCTAAGGAGG AGCAGC CTG AGCCTG GLN GLU SER LEU ARG SER LYS GLU ***CAR GAR WSN YTN MGN WSN AAR GAR TRR--- --- --- --- --- --- --- --- ---CAA GAA TCT TTA CGT TCT AAA GAA TAACAG GAG TCC TTG CGC TCC AAG GAG TAGTCA CTT CGA TCATGATCG CTC CGG TCGAGT CTA AGA AGTAGC CTG AGG AGC

0195 Delivery and expression of nucleic acids in many formulations is limited due to degradation of the nucleic acids by components of organisms, such as nucleases. Thus, protection of the nucleic acids when delivered in vivo can greatly enhance the resulting expression, thereby enhancing a desired pharmacological or therapeutic effect. It was found that certain types of compounds which interact with a nucleic acid (e.g., DNA) in solution but do not condense the nucleic acid provide in vivo protection to the nucleic acid, and correspondingly enhance the expression of an encoded gene product. 0196 We have described the use of delivery systems designed to interact with plasmids and protect plasmids from rapid extracellular nuclease degradation Mumper, R. J., et al., 1996, Pharm. Res. 13:701-709; Mumper, R. J., et al., 1997. Submitted to Gene Therapy. A characteristic of the PINC systems is that they are non-condensing systems that allow the plasmid to maintain flexibility and diffuse freely throughout the muscle while being protected from nuclease degradation. While the PINC systems are primarily discussed below, it will be understood that cationic lipid based systems and systems utilizing both PINCS and cationic lipids are also within the scope of the present invention. 0197 A common structural component of the PINC systems is that they are amphiphilic molecules, having both a hydrophilic and a hydrophobic portion. The hydrophilic portion of the PINC is meant to interact with plasmids by hydrogen bonding (via hydrogen bond acceptor or donor groups), Van der Waals interactions, or/and by ionic interactions. For example, PVP and N-methyl-2-pyrrolidone (NM2P) are hydrogen bond acceptors while PVA and PG are hydrogen bond donors. 0198 All four molecules have been reported to form complexes with various (poly)anionic molecules Buhler V., BASF Aktiengescellschaft Feinchemie, Ludwigshafen, pp 39-42; Galaev Y, et al., J. Chrom. A. 684:45-54 (1994); Tarantino R, et al. J. Pharm. Sci. 83:1213-1216 (1994); Zia, H., et al., Pharm. Res. 8:502-504 (1991);. The hydrophobic portion of the PINC systems is designed to result in a coating on the plasmid rendering its surface more hydrophobic. Kabanov et al. have described previously the use of cationic polyvinyl derivatives for plasmid condensation designed to increase plasmid hydrophobicity, protect plasmid from nuclease degradation, and increase its affinity for biological membranes Kabanov, A. V., and Kabanov, V. A., 1995, Bioconj. Chem. 6:7-20; Kabanov, A. V., et al., 1991, Biopolymers 31:1437-1443; Yaroslavov, A. A., et al., 1996, FEBS Letters 384:177-180. 0199 Substantial protective effect is observed; up to at least a one log enhancement of gene expression in rat muscle over plasmid formulated in saline has been demonstrated with these exemplary PINC systems. We have also found that the expression of reporter genes in muscle using plasmids complexed with the PINC systems was more reproducible than when the plasmid was formulated in saline. For example, the coefficient of variation for reporter gene expression in muscle using plasmid formulated in saline was 9635% (n20 studies; 8-12 muscles/study) whereas with coefficient of variation with plasmids complexed with PINC systems was 4019% (n30 studies; 8-12 muscles/study). The high coefficient of variation for reporter gene expression with plasmid formulated in saline has been described previously 1-5 Davis, H. L., et al., 1993, Hum. Gene Ther. 4:151-9. In addition, in contrast with the results for DNA:saline, there was no significant difference in gene expression in muscle when plasmid with different topologies were complexed with polyvinyl pyrrolidone (PVP). This suggests that PVP is able to protect all forms of the plasmid from rapid nuclease degradation. 0200 1. Summary of Interactions Between a PINC Polymer (PVP) and Plasmid 0201 We have demonstrated using molecular modeling that an exemplary PINC polymer, PVP, forms hydrogen bonds with the base pairs of a plasmid within its major groove and results in a hydrophobic surface on the plasmid due to the vinyl backbone of PVP. These interactions are supported by the modulation of plasmid zeta potential by PVP as well as by the inhibition of ethidium bromide intercalation into complexed plasmid. We have correlated apparent binding between PVP and plasmid to pH and salt concentration and have demonstrated the effect of these parameters on -gal expression after intramuscular injection of plasmid/PVP complexes Mumper, R. J., et al., 1997. Submitted to Gene Therapy. A summary of the physico-chemical properties of plasmid/PVP complexes is listed in Table I below. 14TABLE ISummary of the Physico-Chemical Propertiesof Plasmid/PVP ComplexesMethodResultMolecular modelingHydrogen bonding and hydrophobicplasmid surface observedFourier-transformedHydrogen bonding demonstratedInfra-redDNase I challengeDecreased rate of plasmid degradationin the presence of PVPMicrotitrationPositive heats of reaction indicativeCalorimetryof an endothermic processPotentiometric titrationOne unit pH drop when plasmid and PVPare complexedDynamic DialysisRate of diffusion of PVP reduced in thepresence of plasmidZeta potential modulationSurface charge of plasmid decreased byPVPEthidium bromideEthidium bromide intercalation reducedIntercalationby plasmid/PVP complexationOsmotic pressureHyper-osmotic formulation (i.e., 340mOsm/kg H2O)Luminescence SpectroscopyPlasmid/PVP binding decreased in saltand/or at pH 7

0202 2. Histology of Expression in Muscle 0203 Immunohistochemistry for -gal using a slide scanning technology has revealed the uniform distribution of -gal expression sites across the whole cross-sections of rat tibialis muscles. Very localized areas were stained positive for -gal when CMV--gal plasmid was formulated in saline. -gal positive cells were observed exclusively around the needle tract when plasmid was injected in saline. This is in agreement with previously published results Wolff, J. A., et al., 1990, Science 247:1465-68; Davis, H. L., et al., 1993, Hum. Gene Ther. 4:151-9; Davis, H. L., et al., 1993, Hum. Gene Ther. 4:733-40. 0204 In comparison, immunoreactivity for -gal was observed in a wide area of muscle tissue after intramuscular injection of CMV-p-gal plasmid/PVP complex (1:17 w/w) in 150 mM NaCl. It appeared that the majority of positive muscle fibers were located at the edge of muscle bundles. Thus, staining for -gal in rat muscle demonstrated that, using a plasmid/PVP complex, the number of muscle fibers stained positive for -gal was approximately 8-fold greater than found using a saline formulation. Positively stained muscle fibers were also observed over a much larger area in the muscle tissue using the plasmid/PVP complex providing evidence that the injected plasmid was widely dispersed after intramuscular injection. 0205 We conclude that the enhanced plasmid distribution and expression in rat skeletal muscle was a result of both protection from extracellular nuclease degradation due to complexation and hyper-osmotic effects of the plasmid/PVP complex. However, Dowty and Wolff et al. have demonstrated that osmolarity, up to twice physiologic osmolarity, did not significantly effect gene expression in muscle Dowty, M. E., and Wolff, J. A. In: J. A. Wolff (Ed.), 1994, Gene Therapeutics: Methods and Applications of Direct Gene Transfer. Birkhauser, Boston, pp. 82-98. This suggests that the enhanced expression of plasmid due to PVP complexation is most likely due to nuclease protection and less to osmotic effects. Further, the surface modification of plasmids by PVP (e.g., increased hydrophobicity and decreased negative surface charge) may also facilitate the uptake of plasmids by muscle cells. 0206 3. Structure-Activity Relationship of PINC Polymers 0207 We have found a linear relationship between the structure of a series of co-polymers of vinyl pyrrolidone and vinyl acetate and the levels of gene expression in rat muscle. We have found that the substitution of some vinyl pyrrolidone monomers with vinyl acetate monomers in PVP resulted in a co-polymer with reduced ability to form hydrogen bonds with plasmids. The reduced interaction subsequently led to decreased levels of gene expression in rat muscle after intramuscular injection. The expression of -gal decreased linearly (R0.97) as the extent of vinyl pyrrolidone monomer (VPM) content in the co-polymers decreased. 0208 These data demonstrate that pH and viscosity are not the most important parameters effecting delivery of plasmid to muscle cells since these values were equivalent for all complexes. These data suggest that enhanced binding of the PINC polymers to plasmid results in increased protection and bioavailability of plasmid in muscle. 0209 4. Additional PINC Systems 0210 The structure-activity relationship described above can be used to design novel co-polymers that will also have enhanced interaction with plasmids. It is expected that there is an interactive window of opportunity whereby enhanced binding affinity of the PINC systems will result in a further enhancement of gene expression after their intramuscular injection due to more extensive protection of plasmids from nuclease degradation. It is expected that there will be an optimal interaction beyond which either condensation of plasmids will occur or triplex type formation, either of which can result in decreased bioavailability in muscle and consequently reduced gene expression. 0211 As indicated above, the PINC compounds are generally amphiphilic compounds having both a hydrophobic portion and a hydrophilic portion. In many cases the hydrophilic portion is provided by a polar group. It is recognized in the art that such polar groups can be provided by groups such as, but not limited to, pyrrolidone, alcohol, acetate, amine or heterocyclic groups such as those shown on pp. 2-73 and 2-74 of CRC Handbook of Chemistry and Physics (72nd Edition), David R. Lide, editor, including pyrroles, pyrazoles, imidazoles, triazoles, dithiols, oxazoles, (iso)thiazoles, oxadiazoles, oxatriazoles, diaoxazoles, oxathioles, pyrones, dioxins, pyridines, pyridazines, pyrimidines, pyrazines, piperazines, (iso)oxazines, indoles, indazoles, carpazoles, and purines and derivatives of these groups, hereby incorporated by reference. 0212 Compounds also contain hydrophobic groups which, in the case of a polymer, are typically contained in the backbone of the molecule, but which may also be part of a non-polymeric molecule. Examples of such hydrophobic backbone groups include, but are not limited to, vinyls, ethyls, acrylates, acrylamides, esters, celluloses, amides, hydrides, ethers, carbonates, phosphazenes, sulfones, propylenes, and derivatives of these groups. The polarity characteristics of various groups are quite well known to those skilled in the art as illustrated, for example, by discussions of polarity in any introductory organic chemistry textbook. 0213 The ability of such molecules to interact with nucleic acids is also understood by those skilled in the art, and can be predicted by the use of computer programs which model such intermolecular interactions. Alternatively or in addition to such modeling, effective compounds can readily be identified using one or more of such tests as 1) determination of inhibition of the rate of nuclease digestion, 2) alteration of the zeta potential of the DNA, which indicates coating of DNA, 3) or inhibition of the ability of intercalating agents, such as ethidium bromide to intercalate with DNA. 0214 5. Targeting Ligands 0215 In addition to the nucleic acid/PINC complexes described above for delivery and expression of nucleic acid sequences, in particular embodiments it is also useful to provide a targeting ligand in order to preferentially obtain expression in particular tissues, cells, or cellular regions or compartments. 0216 Such a targeted PINC complex includes a PINC system (monomeric or polymeric PINC compound) complexed to plasmid (or other nucleic acid molecule). The PINC system is covalently or non-covalently attached to (bound to) a targeting ligand (TL) which binds to receptors having an affinity for the ligand. Such receptors may be on the surface or within compartments of a cell. Such targeting provides enhanced uptake or intracellular trafficking of the nucleic acid. 0217 The targeting ligand may include, but is not limited to, galactosyl residues, fucosal residues, mannosyl residues, carnitine derivatives, monoclonal antibodies, polyclonal antibodies, peptide ligands, and DNA-binding proteins. Examples of cells which may usefully be targeted include, but are not limited to, antigen-presenting cells, hepatocytes, myocytes, epithelial cells, endothelial cells, and cancer cells. 0218 Formation of such a targeted complex is illustrated by the following example of covalently attached targeting ligand (TL) to PINC system: 0219 TL-PINCPlasmidTL-PINC::::::Plasmid 0220 Formation of such a targeted complex is also illustrated by the following example of non-covalently attached targeting ligand (TL) to PINC system 0221 TL::::::PINCPlasmidTL::::::PINC::::::Plasmid 0222 or alternatively, 0223 PINCPlasmidPINC::::::::PlasmidTLTL::::::PINC:::::::Plasmid 0224 In these examples :::::::: is non-covalent interaction such as ionic, hydrogen-bonding, Van der Waals interaction, hydrophobic interaction, or combinations of such interactions. 0225 A targeting method for cytotoxic agents is described in Subramanian et al., International Application No. PCT/US96/08852, International Publication No. WO 96/39124, hereby incorporated by reference. This application describes the use of polymer affinity systems for targeting cytotoxic materials using a two-step targeting method involving zip polymers, i.e., pairs of interacting polymers. An antibody attached to one of the interacting polymers binds to a cellular target. That polymer then acts as a target for a second polymer attached to a cytotoxic agent. As referenced in Subramanian et al., other two-step (or multi-step) systems for delivery of toxic agents are also described. 0226 In another aspect, nucleic acid coding sequences can be delivered and expressed using a two-step targeting approach involving a non-natural target for a PINC system or PINC-targeting ligand complex. Thus, for example, a PINC-plasmid complex can target a binding pair member which is itself attached to a ligand which binds to a cellular target (e.g., a MAB). Binding pairs for certain of the compounds identified herein as PINC compounds as identified in Subramanian et al. Alternatively, the PINC can be complexed to a tareting ligand, such as an antibody. That antibody can be targeted to a non-natural target which binds to, for example, a second antibody. 0227 III. Model Systems for Evaluation of Interferon Alpha Constructs and Formulations 0228 In accord with the concept of using interferon alpha expressing plasmid constructs and formulations in anti-cancer treatment, murine model systems were utilized based on murine tumor cell lines. The line primarily used was S.C. VII/SF, which is a cell line derived from murine squamous cell carcinoma (S.C.). 0229 Squamous cell carcinoma of the head and neck begins with the cells lining the oral and pharyngeal cavities. Clinical disease progresses via infiltration and spreads into the underlying tissues and lymphatics. The undifferentiated, in vivo passage tumor line S.C. VII/SF displays this typical growth pattern. In addition, its rapid growth rate provides a relatively short test period for individual experiments. Other murine tumor cell lines include another SCC line KLN-205, a keratinocyte line 1-7, and a colon adenocarcinoma line MC-38. 0230 An optimal model system preferably satisfies the criteria based on having tumor growth rate in vivo (i.e., tumors are ready for treatment in 4-10 days post implant), invasiveness, and local spread similar to those observed in clinical disease, and providing accessibility for experimental treatment. As indicated, the SCC VII/SF cell line was utilized as the primary model system cell line. This cell line typically grows rapidly, resulting in death of untreated syngeneic mice 14-17 days after tumor cell implantation. 0231 This cell line can be utilized in a variety of ways to provide model system suitable for a variety of different tests. Four such possibilities are described below. 0232 First, SCCVII cells can be utilized in cell culture to provide an in vitro evaluation of interferon alpha expression construct and formulation characteristics, such as expression levels and cellular toxicities. 0233 Second, the cells can be implanted subcutaneously in mice. This system can be utilized in tests in which accessibility of the implant site is beneficial. As an example, the method was utilized in evaluations of expression efficiencies based on the expression of chloramphenicol acetyltransferase (CAT). 0234 Third, the cells can be implanted transcutaneously into the fascia of digastric muscle. 0235 Fourth, the cells can be implanted transcutaneously into digrastric/mylohyoid muscles. The important features of models 3 and 4 are shown in the table below. 15TABLE IComparison of submandibular tumor modelsFeatureMouse Tumor Model 3Mouse Tumor Model 4Tumor implant procedure2-4 105 cells transcutaneously into5 105 transcutaneously intofascia of digastric muscledigastric/mylohyoid musclesTumor growth andProminent submandibular bulge;More variable, invasion ofinvasiveness characteristicsinvasion of digastric/mylohyoiddigastric/mylohyoid muscles andmuscles and lymphaticslymphaticsTreatment procedureTranscutaneous, needle inserted andLower jaw skin flap raised to expose(primary treatment)moved within tumor to produce a 4tumor, needle inserted and movedquadrant distribution of genewithin tumor to produce a 4 quadrantmedicinedistribution of gene medicineDays treated (post-implant)Day 5, day 10 (bothDay 5 (tumor exposed), day 8transcutaneously)(transcutaneously)Measurement procedureExternal calipering 2-3 per weekFirst caliper when tumor exposed foruntil deathtreatment, second caliper at sacrificeAdvantagesNon-surgical, closed model allowsSurgical, open model allows directlarger experiments and more frequenttreatment of exposed tumor; Localtreatments; Sacrifice unnecessary toinflammation from surgery maycaliper ( more time points)additionally stimulate immuneresponse; More like clinical situationfor protocol developmentDisadvantagesTranscutaneous treatment isLabor intensive; Smaller, fewerpotentially less accurate andexperiments possible; Tumors deeperintensive; less like expected clinicaland more difficult to treattreatments than surgical approachestranscutaneously (for secondarytreatments); Fewer treatments andcaliperings possible

0236 The tumor size treated in the mouse models is generally 20-50 mm3. A 50 mm3 mouse tumor is approximately equivalent to 150 cc3 human tumor having an average diameter of about 6.6 cm. This tumor size is approximately 10-fold larger than the size proposed to be treated in the phase I clinical trials. This indicates that the mouse models are strongly biased towards over estimating the expected tumor burden in human patients. 0237 IV. Formulations for in vivo Delivery 0238 A. General 0239 While expression systems such as those described above provide the potential for expression when delivered to an appropriate location, it is beneficial to provide the expression system construct(s) in a delivery system which can assist both the delivery and the cellular uptake of the construct. Thus, this invention also provides particular formulations which include one or more expression system constructs (e.g., DNA plasmids as described above), and a protective, interactive non-condensing compound. 0240 An additional significant factor relating to the plasmid construct is the percentage of plasmids which are in a supercoiled (SC) form rather than the open circular (OC) form. 0241 B. Delivery and Expression 0242 A variety of delivery methods can be used with the constructs and formulations described above, in particular, delivery by injection to the site of a tumor can be used. The submandibular tumor models utilized injection into four quadrants of the tumor being treated. 0243 C. Anti-Cancer Efficacy of Human Interferon Alpha Formulations 0244 The effects of the administration of the interferon alpha formulations described above were evaluated using the S.C. VII mouse tumor models. Plasmid constructs as described above were incorporated in delivery formulations. The formulations were delivered by injection. 0245 D. Synergistic Effects of Interferon Alpha Plasmid and IL-12 Plasmid and Effect of Human Interferon Alpha Formulation Administration on Production of Secondary Cytokines 0246 The effects of the expression of the human interferon alpha plasmids in tumor cells on the progress of the mouse tumors demonstrates that such interferon alpha expression is effective against such tumors. However, it was also shown that IL-12 can act synergistically with the interferon alpha expression to exercise the antitumor effect (see FIG. 9). 0247 E. Toxicity Evaluation of Exemplary Formulations 0248 The exemplary formulations do not show high cellular toxicity at the concentrations tested, suggesting that the formulations do not significantly kill cells by direct toxic action in vivo. Moreover, the anti-tumor activity induced by IFN gene therapy is dependent upon activation of the immune system, which is demonstrated by depletion studies in vivo. Removal of a specific T lymphocyte population (CD8) abrogates the anti-tumor activity elicited by IFN gene therapy. 0249 V. Administration 0250 Administration as used herein refers to the route of introduction of a plasmid or carrier of DNA into the body. In addition to the methods of delivery described above, the expression systems constructs and the delivery system formulations can be administered by a variety of different methods. 0251 Administration can be directly to a target tissue or by targeted delivery to the target tissue after systemic administration. In particular, the present invention can be used for treating disease by administration of the expression system or formulation to the body in order to establishing controlled expression of any specific nucleic acid sequence within tissues at certain levels that are useful for gene therapy. 0252 The preferred means for administration of vector (plasmid) and use of formulations for delivery are described above. The preferred embodiments are by direct injection using needle injection. 0253 The route of administration of any selected vector construct will depend on the particular use for the expression vectors. In general, a specific formulation for each vector construct used will focus on vector uptake with regard to the particular targeted tissue, followed by demonstration of efficacy. Uptake studies will include uptake assays to evaluate cellular uptake of the vectors and expression of the DNA of choice. Such assays will also determine the localization of the target DNA after uptake, and establishing the requirements for maintenance of steady-state concentrations of expressed protein. Efficacy and cytotoxicity can then be tested. 0254 Toxicity will not only include cell viability but also cell function. 0255 Muscle cells have the unique ability to take up DNA from the extracellular space after simple injection of DNA particles as a solution, suspension, or colloid into the muscle. Expression of DNA by this method can be sustained for several months. 0256 Delivery of formulated DNA vectors involves incorporating DNA into macromolecular complexes that undergo endocytosis by the target cell. Such complexes may include lipids, proteins, carbohydrates, synthetic organic compounds, or inorganic compounds. Preferably, the complex includes DNA, a cationic lipid, and a neutral lipid in particular proportions. The characteristics of the complex formed with the vector (size, charge, surface characteristics, composition) determines the bioavailability of the vector within the body. Other elements of the formulation function as ligand which interact with specific receptors on the surface or interior of the cell. Other elements of the formulation function to enhance entry into the cell, release from the endosome, and entry into the nucleus. 0257 Delivery can also be through use of DNA transporters. DNA transporters refers to molecules which bind to DNA vectors and are capable of being taken up by epidermal cells. DNA transporters contain a molecular complex capable of noncovalently binding to DNA and efficiently transporting the DNA through the cell membrane. It is preferable that the transporter also transport the DNA through the nuclear membrane. See, e.g., the following applications all of which (including drawings) are hereby incorporated by reference herein: (1) Woo et al., U.S. Ser. No. 07/855,389, entitled A DNA Transporter System and Method of Use, filed Mar. 20, 1992, now abandoned; (2) Woo et al., PCT/US93/02725, International Publ. WO93/18759, entitled A DNA Transporter System and Method of Use, (designating the U.S. and other countries) filed Mar. 19, 1993; (3) continuation-in-part application by Woo et al., entitled Nucleic Acid Transporter Systems and Methods of Use, filed Dec. 14, 1993, U.S. Ser. No. 08/167,641; (4) Szoka et al. , U.S. Ser. No. 07/913,669, entitled Self-Assembling Polynucleotide Delivery System, filed Jul. 14, 1992 and (5) Szoka et al., PCT/US93/03406, International Publ. WO93/19768 entitled Self-Assembling Polynucleotide Delivery System, (designating the U.S. and other countries) filed Apr. 5, 1993. A DNA transporter system can consist of particles containing several elements that are independently and non-covalently bound to DNA. Each element consists of a ligand which recognizes specific receptors or other functional groups such as a protein complexed with a cationic group that binds to DNA. Examples of cations which may be used are spermine, spermine derivatives, histone, cationic peptides and/or polylysine. One element is capable of binding both to the DNA vector and to a cell surface receptor on the target cell. Examples of such elements are organic compounds which interact with the asialoglycoprotein receptor, the folate receptor, the mannose-6-phosphate receptor, or the carnitine receptor. A second element is capable of binding both to the DNA vector and to a receptor on the nuclear membrane. The nuclear ligand is capable of recognizing and transporting a transporter system through a nuclear membrane. An example of such ligand is the nuclear targeting sequence from SV40 large T antigen or histone. A third element is capable of binding to both the DNA vector and to elements which induce episomal lysis. Examples include inactivated virus particles such as adenovirus, peptides related to influenza virus hemagglutinin, or the GALA peptide described in the Szoka patent cited above. 0258 Transfer of genes directly into a tumor has been very effective. Experiments show that administration by direct injection of DNA into tumor cells results in expression of the gene in the area of injection. Injection of plasmids containing human interferon alpha results in expression of the gene for 5 days following a single intra-tumoral injection. Human IFN production was highest in tumors harvested 1 day post-tumor injection and steadily declined thereafter. The injected DNA appears to persist in an unintegrated extrachromosomal state. This means of transfer is a preferred embodiment. 0259 Administration may also involve lipids as described in preferred embodiments above. The lipids may form liposomes which are hollow spherical vesicles composed of lipids arranged in unilamellar, bilamellar, or multilamellar fashion and an internal aqueous space for entrapping water soluble compounds, such as DNA, ranging in size from 0.05 to several microns in diameter. Lipids may be useful without forming liposomes. Specific examples include the use of cationic lipids and complexes containing DOPE which interact with DNA and with the membrane of the target cell to facilitate entry of DNA into the cell. 0260 Gene delivery can also be performed by transplanting genetically engineered cells. For example, immature muscle cells called myoblasts may be used to carry genes into the muscle fibers. Myoblast genetically engineered to express recombinant human growth hormone can secrete the growth hormone into the animal's blood. Secretion of the incorporated gene can be sustained over periods up to 3 months. 0261 Myoblasts eventually differentiate and fuse to existing muscle tissue. Because the cell is incorporated into an existing structure, it is not just tolerated but nurtured. Myoblasts can easily be obtained by taking muscle tissue from an individual who needs gene therapy and the genetically engineered cells can also be easily put back with out causing damage to the patient's muscle. Similarly, keratinocytes may be used to delivery genes to tissues. Large numbers of keratinocytes can be generated by cultivation of a small biopsy. The cultures can be prepared as stratified sheets and when grafted to humans, generate epidermis which continues to improve in histotypic quality over many years. The keratinocytes are genetically engineered while in culture by transfecting the keratinocytes with the appropriate vector. Although keratinocytes are separated from the circulation by the basement membrane dividing the epidermis from the dermis, human keratinocytes secrete into circulation the protein produced. 0262 The chosen method of delivery should result in expression of the gene product encoded within the nucleic acid cassette at levels which exert an appropriate biological effect. The rate of expression will depend upon the disease, the pharmacokinetics of the vector and gene product, and the route of administration, but should be in the range 0.001-100 mg/kg of body weight/day, and preferably 0.01-10 mg/kg of body weight/day. This level is readily determinable by standard methods. It could be more or less depending on the optimal dosing. The duration of treatment will extend through the course of the disease symptoms, possibly continuously. The number of doses will depend upon the disease, delivery vehicle, and efficacy data from clinical trials.

EXAMPLES 0263 The present invention will be more fully described in conjunction with the following specific examples which are not to be construed in any way as limiting the scope of the invention. As shown below, mIFN- gene medicine reduces the growth of tumors in syngeneic murine tumor models. Lipid formulations of mIFN- gene medicine display anti tumor activity in both SCC-VII and MC-38 tumor models. PINC and peptide formulations of mIFN- gene medicine display anti tumor effects in the MC-38 tumor model. The anti tumor effects of mIFN- gene medicine are dose dependent. In addition, the examples demonstrate that treatment of tumors with the combination of IFN and IL-12 gives an unanticipated more than additive (synergystic) anti-tumor activity using either a PINC or a lipid formulation.

Example 1 0264 A plasmid expression system encoding murine IFN4 and formulated in a polymeric delivery system was used for in vivo immunotherapeutic activity against an immunogenic murine renal cell carcinoma, Renca, and a non-immunogenic mammary adenocarcinoma, TS/A. Mice bearing established tumors were treated with IFN/polyvinyl-pyrrolidone (PVP) expression complexes via direct intra-tumoral injection. Up to 100% tumor growth inhibition was observed in the treated mice. By using an optimal dose of 96 and 48 g of formulated IFN- plasmid for the treatment of Renca and TS/A respectively, 30% (Renca) and 10% (TS/A) of the treated animals remained tumor-free. Tumor inhibition was dependent upon activation of the immune system. The anti-tumor activity elicited by IFN- gene therapy was abrogated when mice were selectively depleted of CD8 T cells. By contrast, removal of CD4 resulted in increased tumor rejection following IFN-/PVP treatments. Finally, mice that remained tumor-free following IFN- gene therapy displayed immune resistance to a subsequent challenge of tumor. These data provide evidence that non-viral IFN gene therapy can be used to induce an efficient anti-tumor response. 0265 Local presence of cytokines in tumors can activate an immune response that in some cases leads to induction of specific long-lasting anti-tumor immunity. By direct intra-tumoral injection of plasmid encoding murine IFN4 and formulated in a polymeric delivery system, tumor-bearing mice develop an immune response, which leads to inhibition and eradication of the tumor. We have shown by depletion studies in vivo that the immune response induced by IFN is mainly CD8-mediated and that this treatment results in a long-term immunity in mice demonstrating complete tumor regression. Thus, non-viral IFN gene therapy may be an effective alternative to IFN protein therapy for human cancers. 0266 Transduction of tumor cells with cytokine genes has proven to be a very efficient technique to induce cytokine-mediated anti-tumor immunity. In experimental models, the local presence of IL-2, IL-1, IL-4, IL-6, IL-7, IL-12, IFNs and CSFs (i.e., GM-CSF) at the site of the tumor can result in significant tumor growth inhibition (Colombo et al., Local Cytokine Availability Elicits Tumor Rejection and Systemic Immunity Through Granulocyte-T-Lymphocyte Cross-Talk, Cancer Research, 52, 4853-4857 (1992)). In these systems, cytokines have limited effect on tumor proliferation directly but are capable of activating a rapid and potent anti-tumor immune response, which impedes tumor progression. Established parental tumors, however, are difficult to eradicate with ex vivo cytokine-transduced tumor cells because efficacy of vaccination is highly dependent on the size, growth rate and invasiveness of the tumor. 0267 To overcome these problems, cytokine-based gene therapy approaches, which can deliver transgenic cytokines locally and induce an anti-tumor immune response, have been recently evaluated by a number of investigators (Formi et al., Cytokine-Induced Immunogenicity: From Exogenous Cytokines to Gene Therapy, Journal of Immunotherapy, 14, 253-257, (1993); Pericle et al., An Efficient Th2-type Memory Follows Cd8 Lymphocyte-driven and Eosinophil-mediated Rejection of a Spontaneous Mouse Mamary Adenocarcicoma Engineered to Release II-4, The Journal of Immunology, 153, 5660-5673. (1994); Pardoll et al., Gene Modified Tumor Vaccines, In Cytokine-Induced Tumor Immunogenicity, eds. Academic Press, London, p. 71-86. (1994); and Musiani et al., Cytokines, Tumor-cell Death and Immunogenicity: A Question of Choice, Immunology Today. 1, 32-36 (1997)). Technological breakthroughs in gene therapy using adenoviral, retroviral, and liposomal vectors have provided powerful tools with which to study the biological effects of specific cytokine mediators as well as to develop novel and clinically applicable anti-tumor immunotherapies (Pardoll, Paracrine Cytokine Adjuvants in Cancer Immunotherapy, Annu. Rev. Immunol. 13, 399-415 (1995); Bramson et al., Direct Intratumoral Injection of an Adenovirus Expressing Interleukin-12 Induces Regression and Long-lasting Immunity That Is Associated with Highly Localized Expression of Interleukin-12, Hum. Gene Ther., 7, 1995-2002 (1996); Rao et al., II-12 Is an Effective Adjuvant to Recombinant Vaccinia Virus-based Tumor Vaccines, J. Immunol. 156, 3357-3365. 1996; Rakhmilevich et al., Gene Gun-mediated Skin Transfection with Interleukin 12 Gene Results in Regression of Established Primary and Metastatic Murine Tumors, Proc. Natl. Acad. Sci. USA. 93, 6291-6296 (1996); and Rakhmilevich et al, Cytokine Gene Therapy of Cancer Using Gene Gun Technology: Superior Antitumor Activity of Interleukin-12, Hum. Gene Ther. 8, 1303-1311, (1997)). 0268 A gene therapy approach utilizing an interactive polymeric gene delivery system that increases protein expression by protecting plasmid DNA (pDNA) from nucleases and controlling the dispersion and retention of pDNA in muscle cells is described in Mumper et al., 1996. These polymeric interactive non-condensing (PINC) systems routinely result in a greater amount of gene expression from tissues as compared to delivery of unformulated plasmid in saline (Mumper et al., 1996). By using a plasmid that encodes human insulin growth factor-i (hIGF-1) and formulated as a PINC complex, production of biologically active h IGF-1 in vivo following intramuscular injection has been shown (Alila et al., Expression of Biologically Active Human Insulin-Like Growth Factor-i Following Intramuscular Injection of a Formlated Plasmid in Rats, Human Gene Therapy, 8, 1785-1795 (1997)). The specific objective of this study was to determine whether a plasmid expression system encoding murine IFN4 and formulated as a complex with PVP could induce an anti-tumor immune response following direct injection into subcutaneous murine tumors. 0269 The IFN family consists of three major glycoproteins, IFN, IFN and IFN. Although IFNs were first developed as antiviral agents, it is now clear that they also control cell growth and differentiation, and modulate various aspects of host immunity (Gresser et al., Antitumor effects of interferon, Acta Oncol. 28, 347-353 (1989)). Clinical data concluded that systemic chronic administration of IFN could produce regression of vascular tumors, including Kaposi's sarcoma, pulmonary hemangiomastosis, and hemangiomas (Singh et al., Interferons A and B Down-regulate the Expression of Basic Fibroblast Growth Factor in Human Carcicomas, Proc. Natl. Acad. Sci. USA. 92, 4562-4566 (1995)). Although IFN was the first cytokine to be used in clinical trials that proved to be effective against certain types of human cancer, only recently has this cytokine been considered as a candidate for gene therapy (Ogura et al. 1993, Belldegrun et al., Human Renal Carcinoma Line Transfected With Interleukin-2 and/or Interferon Gene(s): Implications for Live Cancer Vaccines, Journal of the National Cancer Institute, 85, 207-216 (1993). 0270 Initial studies have shown that the injection of genetically modified tumor cells producing IFN into syngeneic mice induces tumor growth inhibition and elicits a tumor-specific immune memory (Ferrantini et al., Interferon Alpha-1-Interferon Gene Transfer into Metastatic Friend Lukemia Cells Abrogated Tumorigenicity in Immunocompetent Mice: Antitumor Therapy by Means of interferon-Producing Cells; Cancer Res. 53, 1107-4615 (1993); Ferrantini et al., Ifn-1 Gene Expression into a Metastatic Murine Adenocarcicoma (Ts/a) Results in Cd8 T Cell-Mediated Tumor Rejection and Development of Antitumor Immunity: Comparative Studies with Ifn--producing Ts/a Cells Journal of Immunology, 153, 4604-4615, (1994); Musiani et al. 1997). However, the real value of this potential form of vaccine in inducing the regression of established tumors remains to be demonstrated. 0271 In this study we present evidence that direct injection of IFN plasmid formulated in PVP into subcutaneous murine tumors results in a host-dependent tumor rejection, primarily mediated by CD8 T cells, and elicits a protective immunity against subsequent tumor re-challenge. 0272 Materials and Methods 0273 Plasmid Construction and Formulation. 0274 A plasmid expression system containing an expression cassette for mIFN-4 was constructed as follows. The coding sequence of the murine IFN-4 gene (Genebank X01973 M15456 M23830 X01967) was amplified by PCR from mouse genomic DNA. The amplified mIFN-4 sequence was then subcloned into a plasmid backbone, and the sequence fidelity was verified by DNA sequence analysis (data not shown). The coding sequence for mIFN-4 was then subcloned as an XbaI-BamH1fragment into the expression plasmid pIL0697 to create the mIFN-4 expression system pIF0836. Plasmid pVC0612 (empty plasmid, EP) contains expression elements including the cytomegalovirus immediate early promoter and the 3 UTR/poly(A) signal from the bovine growth gene in the pVC0289 backbone described by Alila et al. (1997). Plasmid pVC0612 was used as a control plasmid in all in vivo experiments. Plasmids for intra-tumoral injection were grown under kanamycin selection in E. coli host strains DH5 and purified using conventional alkaline lysis and chromatographic methods. Purified plasmid utilized for intra-tumoral injections had the following specifications: endotoxin (<500 Eu/mg plasmid); protein (<1%); and chromosomal DNA (<20%). Purified pIF0836 and control plasmids were formulated at a concentration of 3 mg DNA/ml in a solution of 5% w/v polyvinyl-pyrrolidone (Plasdone C-30, ISP Technologies, Wayne, N.J.), 150 mM NaCl on the day of injection, as described previously (Mumper et al., 1996). 0275 Western Blot Analysis and Bioassay for mIFN. 0276 HeLa cells were plated in 6 well plates at 3105 cells per well, and transfected using 1 g of mouse IFN4 plasmid pIF0836C and 3 g of Lipofectamine (Life Technologies, Inc., Gaithersburg, Md.) in serum-free DMEM. Same supernatants were harvested 24 hours later and immunoprecipitated using anti-mouse interferon / polyclonal antibody (BioSource International, Camarillo, Calif.) and protein A and G agarose (Boehringer Mannheim, Indianapolis, Ind.). Samples were run on a 12% Tris-glycine gel and electroblotted to Millipore PVDF membrane. Anti-mouse interferon / polyclonal antibody was used at 1:1000, followed by anti-sheep Ig HRP (Boehringer Mannheim) at 1:1000. Biotinylated molecular weight markers were detected using Streptavidin-HRP (Amersham, Arlington Heights, Ill.). Detection was performed using the Amersham ECL kit. Supernatants were also tested for IFN biological activity using L929 cells treated with encephalomyocarditis virus, in parallel with a NIH mouse IFN reference reagent (Access Biomedical, San Diego, Calif.). 0277 Animals 0278 Normal 8-week-old female BALB/c mice were purchased from Harlan Laboratories, Houston, Tex. Mice were maintained on ad libitum rodent feed and water at 23 C., 40% humidity, and a 12-h/12-h light-dark cycle. Animals were acclimated for at least 4 days before the start of the study. 0279 Tumors 0280 Three established mouse tumor models were used in this study. TS/A is a tumor cell line established by Dr. P. Nanni, University of Bologna, Italy, from the first in vivo transplant of a moderately differentiated mammary adenocarcinoma that spontaneously arose in a BALB/c mouse (Nanni et al., 1983). A number of pre-immunization-challenge experiments suggested that TS/A does not elicit a long-lasting anti-tumor immunity (Fomi et al., 1987). TS/A was generously provided by Dr. Guido Fomi, University of Turin, Italy. Renca, a spontaneously arising murine renal cell carcinoma, and CT-26, a colon adenocarcinoma, were generously provided by Dr. Drew M. Pardoll, John Hopkins Hospital, Baltimore, Md. Tumor cell cultures were maintained in sterile disposable flasks from Coming (Corning, N.Y.) at 37 C. in a humidified 5% CO2 atmosphere, using RPMI 1640 supplemented with 10% FBS, 100 U/ml penicillin, 100 U/ml streptomycin and 50 g/ml gentamycin; all from Life Technologies. 0281 In vivo Evaluation of Tumor Growth and Treatments 0282 BALB/c mice were challenged s.c. in the middle of the left flank with 30 l of a single-cell suspension contained the specified number of cells. Seven days later when the tumor size reached approximately 10 mm3, treatments with IFN/PVP or EP/PVP started and were repeated at 1-2 day intervals for 2 weeks (total of 8 treatments: 4/week). Tumor volume was measured with electronic caliper in the two perpendicular diameters and in the depth. Measurements of the tumor masses (mm3) were performed twice a week for 40-50 days. All mice bearing tumor masses exceeding 1 cm3 volume were sacrificed for humane reasons. When depletion of immunocompetent cells in vivo was required, a group of mice received i.v 0.5 ml of -CD4 (GK1.5 hybridoma, 207-TIB, ATCC, Rockville, Md.) ascite (1:10), or -CD8 (2.43 hybridoma, 210-TIB, ATCC) ascite (1:100) or i.p. 100 g -GR1 (RB6-8C5 hybridoma, Pharmingen, San Diego, Calif.). Control mice received i.v. 0.5 ml isotype control IgG (Pharmingen). Antibody treatments were performed twice: first injection 1 day before starting the gene therapy treatment and the second injection (i.p at the same dosage) 7 days later. 0283 CTL Assay. 0284 A standard 6-hour 51-chromium (51Cr)-release assay was performed following 5 days of in vitro effector cell stimulation. Single cell suspensions of splenocytes were prepared 3 weeks following tumor challenge by mashing the spleens in RPMI 1640 medium (Life Technologies) and passing the cells through 70 m nylon mesh cell strainers (Falcon, Becton Dickinson, Lincoln Park, N.J.) into 50 ml centrifuge tubes (Falcon). After centrifugation, red blood cells were lysed with ACK Lysing Buffer (Biofluids, Inc., Rockville, Md.) and the splenocytes washed twice with RPMI. In vitro stimulation cultures contained 3106 splenocytes/effectors per ml with 6105 mitomycin-C-treated Renca/stimulator cells per ml and 10 Units per ml recombinant murine IL-2 (Genzyme, Cambridge, Mass.) in RPMI containing 10% FBS, 22 mM HEPES buffer (Research Organics Inc., Cleveland Ohio), Penn-Streptomycin, 5105 M 2--mercapto-ethanol (Life Technologies), OPI media supplement (Sigma, St. Louis, Mo.), and essential and non-essential amino acids (Life Technologies) (for a 5:1 responder: stimulator ratio). Stimulators were prepared by incubating Renca cells at 3107 per ml in RPMI with 30 g per ml mitomycin-C (Sigma) at 37 C. for 60 minutes, followed by four washes in HBSS with 2.5% FBS. After 5 days at 37 C., effector cells were pelleted, resuspended in complete RPMI, counted, and mixed with 51Cr-labeled targets in a 96 well V-bottomed plate (Costar/Corning, Cambridge, Mass.). Renca and CT26 targets were labeled by incubating them at 2106 cells per ml in complete RPMI with 150 uCi 51Cr (Amersham) for 2.5 hours. Targets were washed 3 times in HBSS with 2.5% FBS and resuspended in complete RPMI before addition to the assay. After mixing effectors and targets (in triplicate wells) and a brief pelleting, plates were placed at 37 C. for 6 hours. Approximately 90% of the supernatants were then collected from each well with the Skatron Harvesting Press and Supernatant Collection System (Skatron Instruments, Norway). 51Cr release was detected using a WALLAC 1470 Wizard automatic gamma counter (WALLAC Inc., Gaithersburg Md.). Specific release was determined with the following equation: (experimental cpmspontaneous cpm)/(total cpmspontaneous cpm)100. Spontaneous release from the targets was less than 18%, and the standard error of the triplicate experimental counts was less than 14%. 0285 Statistical Analysis. 0286 Data for the effects of mIFN-. gene therapy on tumor growth were analyzed by repeated measures analysis. Individual treatment means were compared using Duncan's multiple range test when the main effect was significant. Data for the effect of mIFN- gene therapy on tumor rejection were analyzed by ANOVA. In all cases a p value of less than 0.05 was considered to be statistically significant. 0287 Results 0288 Expression of mIFN-0289 Murine IFN- expression plasmid (pIF0836) was transfected into Cos-1 cells, and the resulting conditioned media was assayed for mIFN- by Western blot and by bioassay. Western blot analysis of conditioned media indicated that the recombinant mIFN- expressed from pIF0836 template was present as a single band with an approximate molecular weight of 23 kDa. This band was not observed in conditioned media from mock-transfected cells and likely represents a glycosylated form of mIFN-. Recombinant mIFN- ran with an approximate molecular weight of 18 kDa, which corresponds to the predicted molecular weight of non-glycosylated mIFN-. Assay of conditioned media using an anti-viral bioassay for mIFN- indicated that approximately 175103 IU/ml mIFN- were present. 0290 Anti-tumor activity of IFN- gene therapy. The anti-tumor effect of murine IFN4 plasmid formulated as a complex with PVP (IFN/PVP) was tested in a syngeneic murine renal cell carcinoma (Renca) and a mammary adenocarcinoma (TS/A) tumor model. BALB/c mice were challenged subcutaneously with 7105 Renca or 1105 CT26 cells, and IFN/PVP injections were initiated 7 days later when tumors reached approximately 10 mm3 size. Each group of mice received at interval of 1-2 days 8 treatments (4 injections/week) of IFN/PVP at scalar doses (from 12 to 96 g/mouse), EP/PVP (96 g/mouse) or no treatments for control (ctrl). Tumor size increased progressively in mice injected with EP/PVP (Renca, TS/A) or low doses of IFN/PVP (TS/A), while tumors in mice injected with each dose of IFN/PVP (Renca) or high dose of IFN/PVP (TS/A) showed marked growth inhibition. 0291 Tumor Growth Inhibition is Associated to Systemic Immune Response. 0292 Treatments of Renca and TS/A tumors with IFN/PVP at 96 g/mouse and 48 g/mouse respectively, induced complete regression in 6 out of 20 (Renca) and 2 out of 20 (TS/A) of challenged mice. To test whether the rejection of these tumors leads to specific immune memory, mice with no tumors for 40-50 days following IFN treatments were re-challenged with a greater number of fresh tumors in the right flank. All mice that rejected primary tumors displayed protection against the second tumor challenge whereas mice used as the control group and injected for the first time with same number of tumor cells (1106 Renca or 2105 TS/A) developed tumors. 0293 To evaluate the requirements for the induction of anti-tumor immune memory, Renca and TS/A were injected into BALB/c rendered immunosuppressed by treatment with anti-CD4, anti-CD8 or anti-polymorphonuclear cells (PMN). Depletion of CD8 T cells allowed both Renca and TS/A to grow in all animals following IFN/PVP treatments, showing that this population is crucial for the immune response induced by IFN gene therapy. No increase in tumor growth was found in mice treated with anti-PMN (-GR1) monoclonal Ab (mAb). Increase in tumor rejection was observed in mice depleted of CD4 T and treated with IFN/PVP suggesting that depletion of CD4 T cells can enhance the anti-tumor effect of IFN gene therapy. 0294 Expression of IFN- within the tumor induces a CTL response. To assess whether CD8 tumor specific CTL were induced in vivo by IFN/PVP treatments, splenocytes from Renca tumor-challenged mice were tested for their cytolytic activity following IFN gene therapy. Cytotoxic activity against Renca, and not against CT26 cells used as control for tumor specificity, was found in 2 of 4 mice that had received IFN gene therapy. Moreover, splenocytes from mice depleted of CD4 T cells and treated with IFN/PVP demonstrated potent CTL activity against Renca cells. By contrast, little CTL activity against Renca cells was evident from splenocytes isolated from mice treated with EP/PVP. 0295 Discussion 0296 The data reported herein demonstrate that direct administration of IFN gene formulated in a polymeric delivery system into subcutaneous renal cell carcinoma and mammary adenocarcinoma inhibits tumor growth and induces a long-lasting immunity to secondary tumor challenges. Of considerable significance is the fact that the anti-tumor response was observed against both an immunogenic carcinoma as well a more aggressive and poorly immunogenic adenocarcinoma, a phenotype which is similar to many spontaneously arising tumors in man. 0297 A variety of genetic abnormalities arise in human cancers that contribute to neoplastic transformation and malignancy. Despite increasing understanding of the molecular basis of cancer, many malignancies remain resistant to established forms of treatment. More recently, molecular genetic interventions have been designed in an attempt to improve the efficacy of immunotherapy. While numerous experimental studies have been performed in murine models with tumor cells transduced with cytokine-gene ex vivo, a major limitation in the translation of this strategy to large-scale human tumor vaccine therapy is the labor intensity and variability of establishing each individual tumor in culture and transducing it with an appropriate vector (i.e., retrovirus). Our approach to this problem is to use a non-viral delivery system to modify tumor cells in vivo with cytokine cDNAs so that the tumor cells can supply the cytokine of interest in a paracrine fashion to the anti-tumor responder cells present within the tumor. 0298 Using a plasmid containing IFN4 gene and formulated in PVP, we have shown that intra-tumoral injections of this DNA-PINC complex can lead to complete tumor regression in 30% of the cases (Renca model) with an overall response rate of 100% tumor growth inhibition. These results are in agreement with a recent study that described an anti-tumor activity elicited by genetically modified TS/A cells producing murine IFN-1 (Ferrantini et al., 1994). Although the anti-tumor effect of IFN using cytokine-gene transduced tumor cells has been described (Scarpa et al., Extracellular Matrix Remodelling in a Murine Mamary Adenocarcicoma Transfected with the Interferon-alpha1 Gene, Journal of Pathology. 181, 116-123 1997), the real value of IFN gene therapy in blocking or inhibiting advanced tumors remains to be explored. The advantage of using a non-viral IFN gene delivery system over retrovirus is that tumor cells could be transduced directly in vivo without the need of first establishing tumor cells in vitro. Moreover, IFN has a potent anti-viral activity limiting the use of this gene in combination with viral vectors. 0299 Therapeutic levels of gene expression for IGF-I using a similar interactive PVP-based delivery system have previusly been described (Alila et al., 1997). Direct intra-tumor injection of the same PINC delivery system as a complex with IFN gene, resulted in dispersion in vivo of plasmid into target cells inducing an IFN-specific anti-tumor activity. Tumors treated with the same plasmid but in the absence of IFN coding region and formulated as a complex with PVP, did not respond to this treatment and grew in a similar rate to untreated tumors. By using an optimal dose of IFN/PVP, tumor-bearing mice were able to reject the tumors mounting a specific long-lasting tumor immunity. Although, the numbers of mice rejecting a second tumor challenge was low, this observation indicates that a considerable portion of the activity of IFN in inducing the rejection of established tumors is not anti-angiogenic or anti-proliferative but immunostimulatory. Our result demonstrating that IFN-induced regression of advanced tumors was prevented by in vivo administration of anti-CD8 mAb provides direct evidence for a key role of CD8 T cells in the anti-tumor effect of IFN. 0300 Depletion of CD4 T cells in tumor-bearing mice treated with IFN gene therapy significantly enhanced the therapeutic effect of IFN, resulting in tumor regression and prolonged survival of up to 80% of treated mice. A CD4-mediated suppression during tumor progression has been previously reported and it has also been shown that depletion of CD4 T cells in tumor-bearing mice results in augmentation of anti-tumor therapy with either IL-2 or IL-12 (Rackmilevich et al., 1994 and Martinotti et al., Cd4 T Cells Inhibit in Vivo the Cd8-Mediated Immune Response Against Murine Colon Carcinoma Cells Transducted with Interleukin-12 Genes, Eur. J. Immunol, 25, 137-146. (1995)). They have shown that depletion of CD4 T cells in tumor-bearing mice in the absence of treatment did not affect the growth of tumor itself suggesting that removal of CD4 T cells does not deprive the tumor of growth factors (Rackmilevich et al., 1994). A possible explanation for this phenomenon is that depletion of CD4 T cells from tumor-bearing mice augments the anti-tumor efficacy of IFN-activated CD8 T cells by releasing them from immunosuppression. The mechanism driving CD4 suppression is poorly understood, although Th2 type cytokines, directly or through B cell activation, may inhibit cell-mediated immunity (Mossmani et al., 1989; Powrie et al., Eur-J-Immunol, 23(11):3043-9 (1993)). CTL can be generated in both CD4-depleted and non-depleted mice from lymphocytes obtained from spleens by in vitro re-stimulation with mitomycin-treated Renca cells and rIL-2. Thus, CD4-mediated suppression appears to be exerted on CD8 expansion and not priming. In accord with the in vivo results, stronger CTL activity was observed from mice depleted of CD4 and treated with IFN/PVP suggesting CD4 T cells inhibit an IFN-mediated CD8 T cell response in vivo. This study suggests that direct administration of cytokine genes, like IFN, into tumors, which have been found to suppress malignancy growth, provide a new therapeutic option for the treatment of human cancers.

Example 2

Pharmacology of mIFN- Gene Medicine in Syngeneic Tumor Models 0301 Gene expression systems encoding either mIFN-2 or mIFN-4 were tested for anti tumor activity when formulated in either cationic lipid, peptide, or PINC delivery systems and injected intratumorally into subcutaneous squamous cell carcinoma (SCC-VII) or adenocarcinoma (MC-38) tumors. 0302 Experimental Design and Treatment Regimen 0303 Experiments to test the anti tumor activity of mIFN- gene medicine were conducted in either SCC-VII or MC-38 tumor models. Tumor cells (4105) were injected subcutaneously into the flank region of mice, and treatment was initiated when tumor volume reached approximately 50 mm3. Treatment was begun approximately 6 days (SCC-VII tumors) and 10 days (MC-38 tumors) after tumor initiation and repeated at 3 to 5 day intervals. 0304 All formulations of mIFN- gene medicine were administered in a dose volume of 50 l. The faster growing SCC-VII tumors typically received 3 treatments, whereas the relatively slower growing MC-38 tumors typically received 4 treatments. Experiments were terminated when lactose vehicle control tumors reached approximately 1000 mm3. 0305 The anti-tumor effects of murine IFN gene medicine (IFN/PVP) was tested in syngeneic murine renal cell carcinoma (Renca) and mammary adenocarcinoma (TS/A) tumor model. BALB/c mice were challenged subcutaneously with 7105 or 1105 CT26, and IFN/PVP injections were initiated 7 days later when tumors reached approximately 10 mm3 size. Each group of mice received 8 treatments (4 injections for 2 weeks) of IFN/PVP at scalar doses (from 12 to 96 g/mouse), empty plasmid/PVP (EP/PVP, 96 g/mouse) or no treatments for control (ctrl). Tumor size increased progressively in mice injected with EP/PVP (Renca, TS/A) or low doses of IFN/PVP (TS/A), while tumors in mice injected with each dose of IFN/PVP (Renca) or high dose of IFN/PVP (TS/A) showed marked growth inhibition.

Example 3

mIFN- Gene Medicine Formulated in Cationic Lipid Reduces the Growth of SCC-VII Tumors 0306 Experiments were conducted in the SCC-VII tumor model as described in the preceding example. mIFN- gene medicine formulated in cationic lipid, peptide, and PINC delivery systems was tested. Results show that cationic lipid formulations significantly reduce the growth of SCC-VII tumors relative both to lactose vehicle injected tumors and to tumors injected with control (non coding) plasmid formulated in cationic lipid. The effect of mIFN- gene medicine formulated in cationic lipid is dose dependent and there is no effect of mIFN- gene medicine when formulated in PVA. In addition, analysis of tumors from this experiment using immunohistochemical methods revealed infiltration of CD8 lymphocytes in tumors injected with cationic lipid formulations, but not in tumors injected with PVA formulations. 0307 mIFN- gene medicine significantly reduces the growth of SCC-VII tumors as compared to control plasmid or lactose injected tumors. Differences between control plasmid and mIFN- plasmid were consistent across formulation. Plasmid dose was 46 g/treatment. Growth of tumors injected with control plasmid was compared to that of tumors injected with mIFN- gene medicine using repeated measures analysis. mIFN- reduced SCC-VII tumor growth relative to control plasmid (p0.035).

Example 4

mIFN- Gene Medicine Reduces the Growth of MC-38 Tumors 0308 Experiments were carried out as described in the preceding examples. The effects of various prototype formulations of mIFN- gene medicine on the growth of subcutaneous MC-38 tumors were compared. mIFN- gene medicine elicited reduced tumor growth in all formulations tested (cationic lipid, peptide, and PINC). Subsequent experiments in the MC-38 tumor model have shown similar results.

Example 5

Dose Responses 0309 After demonstrating anti tumor effects of mIFN- gene medicine, the dose response for these effects was investigated in the MC-38 tumor model. Both cationic lipid (DOTMA:Chol) and PINC (PVA) delivery systems were evaluated. Results clearly show that mIFN- gene medicine elicited a dose dependent reduction in tumor growth. Tumor volume in this experiment was maximally reduced by approximately 50% with mIFN-/DOTMA:Chol and 60% with mIFN-/PVA after 4 treatments. Maximal reduction in tumor volume was observed at a plasmid dose of approximately 50 g/treatment (cumulative dose of approximately 200 g). These experiments will be conducted primarily in the MC-38 tumor model because it provides a broader treatment window than does the SCC-VII model.

Example 6

IFN-Alpha Formulations 0310 The formulations for the IFN- are: (1) PVP 4 vial, (2) PVP three vial, (3) PVP two vial. The details are listed below: 0311 PVP 4 Vial 0312 Materials: 25% PVP (50 kDa) stock solution, plasmid stock solution, 5 M NaCl stock solution, and water. 0313 Method: Add in order of water, plasmid, 25% PVP and 5 M NaCl into a vial to make a plasmid in 5% PVP in saline formulation. The final concentration of PVP and NaCl are fixed (5% and 150 mM) and plasmid concentration could be varied (but based on the IGF-1 data, 3 mg DNA/ml in 5% PVP in saline should be the best formulation). The quality of the formulation is characterized by pH, DNA concentration, osmolality, and gel electrophoresis. The DNA concentration could be varied from 0.1-5 mg/ml. The pH may be varied from 3-5, osmolality may be 250-400 mOsm. 0314 Three Vial 0315 Material: lyophilized PVP, plasmid stock solution (4 mg/ml), 115 mM Na-Citrate/5% NaCl stock buffer (pH4). 0316 Method: Add in order of plasmid and buffer into the PVP to make final 3 mg DNA/ml in 5% PVP in 25 mM citrate/saline buffer (pH4). DNA expression is higher in saline than in the citrate buffer. 0317 Two Vial 0318 Materials: Co-lyophilized plasmid and PVP, saline. Add saline into the co-lyophilized DNA and PVP to make final 3 mg/ml DNA in 5% PVP in saline. 0319 The final formulation is 3 mg/mL DNA, 5% PVP as a single vial. The formulation is prepared by adding (5%) PVP to (4 mg/mL) DNA and recirculating the two components for a finite period of time (using static mixer). Then the formulation is lyophilized and rehydrated with 0.9% sodium chloride, to obtain a final composition of 3 mg/mL, 5%PVP in saline.

Example 7

Treatment of Human Tumors 0320 The murine studies are predictive of the response of Human tumors to therapy using a plasmid construct encoding the human IFN alpha gene sequence such as that depicted in SEQ ID NO: 10, 11 or 12. A patient in need of anti-cancer therapy is injected with up to 3 mg of plasmid formulation at daily intervals. The plasmid formulation may contain INF alpha plasmid alone or optionally a mixture of IFN-alpha encoding plasmid and an additional plasmid coding for a cytokine. The preffered cytokine is IL-12. The treatments are continued and the patient monitored as is the usual practice for anti-cancer chemotherapeutic regimes. 0321 One skilled in the art would readily appreciate that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The molecular complexes and the methods, procedures, treatments, molecules, specific compounds described herein are presently representative of preferred embodiments are exemplary and are not intended as limitations on the scope of the invention. Changes therein and other uses will occur to those skilled in the art which are encompassed within the spirit of the invention are defined by the scope of the claims. 0322 It will be readily apparent to one skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention. All patents and publications mentioned in the specification are indicative of the levels of those skilled in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.