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References
Andersen, J.K., Garber, D.A., Meaney, C.A., and Breakefield, X.O. (1992). “Gene transfer into mammalian central nervous system using herpes virus vectors: extended expression of bacterial lacZ in neurons using the neuron-specific enolase promoter”. Hum. Gene. Ther., 3(5), 487–499.
Boviatsis, E.J., Scharf, J.M., Chase, M., Harrington, K., Kowall, N.W., Breakefield, X.O., and Chiocca, E.A. (1994). “Antitumor activity and reporter gene transfer into rat brain neoplasms inoculated with herpes simplex virus vectors defective in thymidine kinase or ribonucleotide reductase”. Gene. Ther., 1(5), 323–331.
Chambers, R., Gillespie, G.Y., Soroceanu, L., Andreansky, S., Chatterjee, S., Chou, J., Roizman, B., and Whitley, R.J. (1995). “Comparison of genetically engineered herpes simplex viruses for the treatment of brain tumors in a scid mouse model of human malignant glioma”. Proc. Natl. Acad. Sci. U.S.A., 92(5), 1411–1415.
Chen, S., Li Chen, X.H., Wang, Y., Kosai, K., Finegold, M.J., Rich, S.S., and Woo, S.L. (1995). “Combination gene therapy for liver metastasis of colon carcinoma in vivo”. Proc. Natl. Acad. Sci., 92, 2577–2581.
Chiocca, E.A., Choi, B.B., Cai, W.Z., DeLuca, N.A., Schaffer, P.A., DiFiglia, M., Breakefield, X.O., and Martuza, R.L. (1990). “Transfer and expression of the lacZ gene in rat brain neurons by herpes simplex virus mutants”. New Biol., 2, 739–746.
Collins, M.K., Takeuchi, Y., Cosset, F.L., Tailor, C., and Weiss, R.A. (1994). “Development of recombinant retroviruses suitable for in vivo gene delivery”. Cold Spring Harbor Meeting: Gene Therapy, Sept. 1994, 97.
Dranoff, G., Jaffee, E., Lazenby, A., Golumbek, P., Levitsky, H., Brose, K., Jackson, V., Hamada, H., Pardoll, D., and Mulligan, R. (1993). “Vaccination with irradiated tumor cells engineered to secrete murine GM-CSF stimulates potent, specific and long lasting anti-tumor immunity”. Proc. Natl. Acad. Sci. (USA), 90, 3539–3543.
During, M.J., Naegele, J.R., O’Malley, K.L., and Geller, A.I. (1994). “Long-term behavioral recovery in Parkinsonian rats by an HSV vector expressing tyrosine hydroxylase”. Science, 266, 1399–1403.
Fearon, E.R., Pardoll, D.M., Itaya, T., Golumbek, P., Levitsky, H.I., Simons, J.W., Karasuyama, H., Vogelstein, B., and Frost, P. (1990). “Interleukin-2 production by tumor cells bypasses T helper function in the generation of an antitumor response”. Cell, 60, 397–403.
Galili, U., (1993). “Evolution and pathophysiology of the human natural anti-alpha-galactosyl IgG (anti-Gal) antibody”. Springer Semin Immunopathol, 15, 155.
Galili, U., and Latemple, D.C. (1997). “Natural anti-gal antibody as a universal augmentor of autologous tumor vaccine immunogenicity”. Immunol Today, 18, 281–285.
Galili, U., Shohet, S.B., Kobrin, E., Stults, C.L., and Macher, B.A. (1988). “Man, apes, and Old World monkeys differ from other mammals in the expression of alpha-galactosyl epitopes on nucleated cells”. J. Biol. Chem., 263(33), 17755–17762.
Galili, U, Tibell, A., Samuelsson, B., Rydberg, L., and Groth, C.G. (1995). “Increased anti-Gal activity in diabetic patients transplanted with fetal porcine islet cell clusters”. Transplantation, 59(11), 1549–1556.
Geller, A.I., and Breakefield, X.O. (1988). “A defective HSV-1 vector expresses Escherichia coli β-galactosidase in cultured peripheral neurons”. Science, 241, 1667–1669.
Geller, A.I., and Freese, A. (1990). “Infection of cultured central nervous system neurons with a defective herpes simplex virus 1 vector results in stable expression of Escherichia coli beta-galactosidase”. Proc. Natl. Acad. Sci. U.S.A., 87, 1149–1153.
Glorioso, J.C., DeLuca, N.A., and Fink, D.J. (1995). “Development and application of herpes simplex virus vectors for human gene therapy”. Annu. Rev. Microbiol., 49, 675–710.
Goldie, J.H., and Coldman, A.J. (1979). “A mathematic model for relating the drug sensitivity of tumors to their spontaneous mutation rate”. Cancer Treat. Rep., 63(11–12), 1727–1733.
Golumbek, P.T., Lazenby, A.J., Levitsky, H.I., Jaffee, L.M., Karasuyama, H., Baker, M., and Pardoll, D.M. (1991). “Treatment of established renal cancer by tumor cells engineered to secrete interleukin-4”. Science, 254, 713–716.
Ho, D., Mocarski, E., and Sapoloski, R. (1993). “Altering central nervous system physiology with a defective herpes simplex virus vector expressing the glucose transporter gene”. Proc. Natl. Acad. Sci. U.S.A., 90, 3655–3659.
Kwong, A.D., and Frenkel, N. (1984). “Herpes simplex virus amplicon: Effect of size on replication of constructed defective genomes containing eukaryotic DNA sequences”. J. Virol., 51, 595–603.
Kwong, A.D., and Frenkel, N. (1985). “The Herpes simplex virus amplicon. Efficient expression of a chimeric chicken ovalbumin gene amplified within defective virus genomes”. Virology, 142, 421–425.
Larsen, R.D., Rajan, V.P., Ruff, M.M., Kukowska-Latallo, J., Cummings, R.D., and Lowe, J.B. (1989). “Isolation of a cDNA encoding a murine UDPgalactose:beta-D-galactosyl-1,4-N-acetyl-D-glucosaminide alpha-1,3-galactosyltransferase: expression cloning by gene transfer”. Proc. Natl. Acad. Sci. U.S.A., 86(21), 8227–8231.
Larsen, R.D., Rivera-Marrero, C.A., Ernst, L.K., Cummings, R.D., and Lowe, J.B. (1990). “Frameshift and nonsense mutations in a human genomic sequence homologous to a murine UDP-Gal:beta-D-Gal(l,4)-D-GlcNAc alpha(l,3)-galactosyltransferase cDNA”. J. Biol. Chem., 265(12), 7055–7061.
Link, C.J., Levy, J.P., Seregina, T., Atchinson, R., and Moorman, D. (1997). “Protection of complement mediated lysis of murine vector producer cells by sCR1 and low molecular weight heparins”. Cancer Gene Therapy, H. Mazarakis and S.J. Swart, eds., 1BC Library Series, London, United Kingdom, 135–152.
Link, C.J., Jr., Moorman, D., Seregina, T, Levy, J.P., and Schabold, K.J. (1996). “A phase I trial of in vivo gene therapy with the herpes simplex thymidine kinase/ganciclovir system for the treatment of refractory or recurrent ovarian cancer”. Hum. Gene. Ther., 7(9), 1161–1179.
Link, C.J., Seregina, T.S., Atchison, R., Hall, A., Muldoon, R., and Levy, J.P. (1998). “Eliciting hyperacute xenograft response to treat uman cancer: α(1,3)galactosyltransferase gene therapy”. Anticancer Res., 18, 2301–2308.
Martuza, R.L., Malick, A., Markert, J.M., Ruffner, K.L., and Coen, D.M. (1991). “Experimental therapy of human glioma by means of a genetically engineered virus mutant”. Science, 252, 854–856.
Miller, A.D., and Buttimore, C. (1986). “Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production”. Molec. Cell Biol., 6, 2895–2902.
Miller, D.G., Adam, M.A., and Miller, A.D. (1990). “Gene transfer by retrovirus vectors occurs in cells that are actively replicating at the time of infection”. Mol. Cell Biol., 10, 4139–4242.
Mineta, T., Markert, J.M., Takamiya, Y., Coen, D.M., Rabkin, S.D., and Martuza, R.L. (1994). “CNS tumor therapy by attenuated herpes simplex viruses”. Gene. Ther., 1(1).
Nabel, G.J., Nabel, E., Yang, Z., Fox, B.A., Plautz, G.E., Gao, X., Huang, L., Shu, S., Gordon, D., and Chang, A.E. (1993). “Direct gene transfer with DNA-liposome complexes in melanoma: Expression, biologic activity, and lack of toxicity in humans”. Proc. Natl. Acad. Sci. (USA), 90, 11307–11311.
Palella, T.D., Hidaka, Y., Silverman, L.J., Levine, M., Glorioso, J., and Kelley, W.N. (1989). “Expression of human HPRT mRNA in brains of mice infected with a recombinant herpes simplex type 1 vector”. Gene., 80, 137–144.
Parker, S.L., Tong, T., Bolden, S., and Wingo, P.A. (1997). “Cancer statistics, 1997”. CA, Cancer J. for Clinicians, 47, 5–27.
Platt, J.L., Vercellotti, G.M., Dalmasso, A.P., Matas, A.J., Bolman, R.M., Najarian, J.S., and Bach, F.H. (1990). “Transplantation of discordant xenografts: a review of progress”. Immunol. Today, 17, 450–457.
Pruitt, S.K., Kirk, A.D., Bollinger, R.R., Marsh, J., Henry, C., Collins, B.H., Levin, J.L., Mault, J.R., Heinle, J.S., Ibrahim, S., Rudolph, A.R., Baldwin, I., William, M., and Sanfilippo, F. (1994). “The effect of soluble complement receptor type 1 on hyperacute rejection of porcine xenografts”. Transplantation, 57, 363–370.
Ram, Z., Culver, K.W., Oshiro, E.M., Viola, J.J., DeVroom, H.L., Otto, E., Long, Z., Chiang, Y., McGarrity, G.J., Muul, L.M., Katz, D., Blaese, R.M., and Oldfield, E.H. (1997). “Therapy of malignant brain tumors by intratumoral implantation of retroviral vector-producing cells [see comments]”. Nat. Med., 3(12), 1354–1361.
Reeves, M.E., Royal, R.E., Lam, J.S., Rosenberg, S.A., and Hwu, P. (1996). “Retroviral transduction of human dendritic cells with a tumor-associated antigen gene”. Cancer Res., 56(24), 5672–5677.
Reisman, D., Yates, J., and Sugden, B. (1985). “A putative origin of replication of plasmids derived from Epstein-Barr virus is composed of two cis-acting components”. Mol. Cell. Biol., 5, 1822–1832.
Roth, J.A., Cristiano, R.J., Roth, J.A., and Cristiano, R.J. (1997). “Gene therapy for cancer: what have we done and where are we going?” J. Natl. Cancer Inst., 89(1), 21–39.
Rother, R.P., Fodor, W.L., Springhorn, J.P., Birks, C.W., Setter, E., Sandrin, M.S., Squinto, S.P., and Rollins, S.A. (1995a). “A novel mechanism of retrovirus inactivation in human serum mediated by anti-alpha-galactosyl natural antibody”. J. Exp. Med., 182(5), 1345–1355.
Rother, R.P., Squinto, S.P., Mason, J.M., and Rollins, S.A. (1995b). “Protection of retroviral vector particles in human blood through complement inhibition”. Hum. Gene. Ther., 6(4), 429–435.
Sandrin, M.S., Vaughan, H.A., Dabkowski, PL., and McKenzie, I.F. (1993). “Anti-pig IgM antibodies in human serum react predominantly with Gal(alpha l-3)Gal epitopes”. Proc. Natl. Acad. Sci. U.S.A., 90(23), 11391–11395.
Schwartz, R.S., Silberstein, L.E., and Berkman, E.M. (1995). “Autoimmune hemolytic anemia”. Hematology Basic Principles and Practice, R. Hoffman, E.J. Benz, S.J. Shattil, B. Furie, H.J. Cohen, and L.E. Silberstein, eds., Churchill Livingstone, New York, 723–724.
Seregina, T., Levy, J., and Link, C. “Development of ganciclovir resistance in cells transduced with the HStk gene”. Fourth International Conference on the Gene Therapy of Cancer, San Diego, CA, A332.
Short, M.P., Choi, B.C., Lee, J.K., Malick, A., Breakefield, X.O., and Martuza, R.L. (1990). “Gene delivery to glioma cells in rat brain by grafting of a retrovirus packaging cell line”. J. Neurosci. Res., 27, 427–439.
Spaete, R.R., and Frenkel, N. (1982). “The herpes simplex virus amplicon: A new eukaryotic defective-virus cloning-amplifying vector”. Cell, 30, 295–304.
Sugden, B., Marsh, K., and Yates, J. (1985). “A vector that replicates as a plasmid and can be efficiently selected in B-lymphoblasts transformed by Epstein-Barr virus”. Molec Cell Biol, 5(2), 410–413.
Takamiya, Y., Short, M.P., Ezzeddine, Z.D., Moolten, F.L., Breakefield, X.O., and Martuza, R.L. (1992). “Gene therapy of malignant brain tumors: a rat glioma line bearing the herpes simplex virus type 1-thymidine kinase gene and wild type retrovirus kills other tumor cells”. J. Neurosci Res., 33(3), 493–503.
Vaughan, H.A., McKenzie, I.F., and Sandrin, M.S. (1995). “Biochemical studies of pig xenoantigens detected by naturally occurring human antibodies and the galactose alpha( l-3)galactose reactive lectin”. Transplantation, 59(1), 102–109.
Wang, S., and Vos, J. (1996). “A hybrid infectious vector based on Epstein-Barr virus and Herpes simplex virus type I for gene transfer into Human Gene”. J Virol, 70, 8422–8430.
Wang, S., Young, W.-B., Jacobson, C., and Link, C.J. (1997). “A novel Herpesvirus amplicon system for in vivo gene therapy”. Gene. Ther., 4, 1132–1141.
Welsh, R.M., Cooper, N.R., Jensen, F.C., and Oldstone, M.B. (1975). “Human serum lyses RNA tumor viruses”. Nature, 257, 612–614.
Witzig, T.E., Ingle, J.N., Schaid, D.J., Wold, L.E., Barlow, J.F., Gonchoroff, N.J., Gerstner, J.B., Krook, J.E., Grant, C.S., and Katzmann, J.A. (1993). “DNA ploidy and percent S-phase as prognostic factors in node-positive breast cancer: results from patients enrolled in two prospective randomized trials”. J. Clin. Oncol., 11(2), 351–359.
Wood, C., Kabat, E.A., Murphy, L.A., and Goldstein, I.J. (1979). “Immunochemical studies on the cpmbining site of two isolectins A4 and B4 isolated from Bandeirea simpliciflia”. Arch. Biochem. Biophys., 198, 1–11.
Yates, J.L., Warren, N., and Sugden, B. (1985). “Stable replication of plasmids derived from Epstein-Barr virus in various mammalian cells”. Nature, 313, 812–815.
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Link, C.J., Hellrung, D.J., Seregina, T., Wang, S. (2002). Eliciting Hyperacute Rejection as a Tumor Killing Strategy. In: Habib, N.A. (eds) Cancer Gene Therapy. Advances in Experimental Medicine and Biology, vol 465. Springer, New York, NY. https://doi.org/10.1007/0-306-46817-4_20
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