Cell-type specific gene transfer using retroviral vectors contai

Chemistry: molecular biology and microbiology – Vector – per se

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536 234, 536 2353, 536 2372, C12N 1586

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active

061468851

ABSTRACT:
The present invention pertains to retroviral vector particles having target cell specificity which comprise a retroviral vector having an antigen binding site of an antibody fused to the envelope protein of the retroviral vector, wherein the antigen binding site of the antibody replaces the natural viral receptor binding site.

REFERENCES:
Orpin et al., "Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy", Dec. 7, 1995.
Verma et al., Nature, vol. 389, pp. 239-242, Sep. 18, 1997.
Eliot Marshall, "Gene Therapy's Growing Pains", Science, vol. 269, Aug. 25, 1995, pp. 1050-1055.
Russell et al., "Retroviral Vectors Displaying Functional Antibody, Fragments", Nucleic Acids Res., vol. 21, No. 5, 1993, pp. 1081-1085.
Kewalramani, V.N., et al. "Spleen Necrosis Virus, an avian innunossupressive retrovirus, shares a receptor with the type D simian retroviruses", Journal of Virology, vol. 66, No. 5, May 1992, pp. 3026-3031.
Riley, S.C., et al. "Preferential expression of variable region heavy chain gene segments by predominant 2,4-dinitrophenyl-specific BALB/c neonatal antibody clonotypes," Proceedings of the National Academy of Sciences of USA, vol. 83, No. 8, Apr. 1986, pp. 2589-2593.
Te-Hua, T.C., et al. "Cell targeting with retroviral vector particles containing antibody-envelope fusion proteins," Gene Therapy, vol. 1, No. 5, Sep. 1994, pp. 292-299.

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