Towards efficient cell targeting by recombinant retroviruses

Molecular Medicine Today

Volumn 3, Issue 9, 1997, Pages 396-403

  Marin, Mariana ^a   Noël, Danièle ^a   Piechaczyk, Marc ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

VIRUS VECTOR;

EXPRESSION VECTOR; GENE TARGETING; GENE TECHNOLOGY; GENETIC RECOMBINATION; HUMAN; NONHUMAN; RETROVIRUS; REVIEW;

GENE THERAPY; GENE TRANSFER TECHNIQUES; GENES, VIRAL; GENETIC ENGINEERING; GENETIC VECTORS; HUMANS; RETROVIRIDAE; VIRAL ENVELOPE PROTEINS;

ANIMALIA; UNIDENTIFIED RETROVIRUS;

EID: 0344505194     PISSN: 13574310     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-4310(97)01095-2     Document Type: Review

References (36)

1. Kay, M. and Woo, S. (1994) Gene therapy for metabolic disorders, Trends Genet. 10, 253-257
2. Crystal, R.G. (1995) Transfer of genes to humans: early lessons and obstacles to success, Science 270, 404-410
3. Vile, R. and Russell, S.J. (1994) Gene transfer technologies for the gene therapy of cancer, Gene Ther. 1, 88-98
4. Günzburg, W. and Salmons, B. (1995) Virus vector design in gene therapy, Mol. Med. Today 2, 410-417
5. Naldini, L. et al. (1996) In vivo gene delivery and stable transduction of non-dividing cells by a lentiviral vector, Science 272, 263-267
6. Miller, N. and Vile, R. (1995) Targeted vectors for gene therapy, FASEB J. 9, 190-199
7. Schnierle, B. and Groner, B. (1996) Retroviral targeted delivery, Gene Ther. 3, 1069-1073
8. Cosset, F-L. and Russell, S. (1996) Targeting retrovirus entry, Gene Ther. 3, 946-956
9. Weiss, R. (1993) Cellular receptors and viral glycoproteins involved in retrovirus entry, in The Retroviridae (Levy, J.A., ed.) pp. 1-108, Plenum Press
10. Weiss, R. and Tailor, C. (1995) Retrovirus receptors, Cell 82, 531-533
11. Rubin, H. (1965) Genetic control of cellular susceptibility to pseudotypes of Rous sarcoma virus. Virology 26, 270-275
12. Burns, J. et al. (1993) Vesicular stomatitis virus G-glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells, Proc. Natl. Acad. Sci. U. S. A. 90, 8033-8037
13. Reiser, J. et al. (1996) Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles, Proc. Natl. Acad. Sci. U. S. A. 93, 15266-15271
14. Roux, P., Jeanteur, P. and Piechaczyk, M. (1989) Cell targeting by recombinant retrovirus using bi-specific antibody complexes, in NATO Advanced Study Institute Series; subseries "Cell Biology", "Vectors as tools for the study of normal and abnormal growth and differentiation" 34, pp. 153-164, Springer-Verlag
15. Roux, P., Jeanteur, P. and Piechaczyk, M. (1989) A versatile and potentially general approach to the targeting of specific cells by retroviruses: application to the infection of human cells by means of major histocompatibility complex class I and class II antigens by mouse ecotropic murine leukemia virus-derived viruses, Proc. Natl. Acad. Sci. U. S. A. 86, 9079-9083
16. Etienne-Julan, M. et al. (1992) The efficiency of cell targeting by recombinant retroviruses depends on the nature of the receptor and the composition of the artificial cell-virus linker, J. Gen. Virol. 73, 3251-3255
17. Cosset, F-L. et al. (1995) Retroviral retargeting by envelopes expressing an N-terminal binding domain, J. Virol. 69, 6314-6322
18. Neda, H., Wu, C. and Wu, G. (1991) Chemical modification of an ecotropic murine leukemia virus results in redirection of its target cell specificity, J. Biol. Chem. 266, 14143-14146
19. Rein, A. et al. (1994) Function of the cytoplasmic domain of a retroviral transmembrane protein: p15E-p2E cleavage activates the membrane fusion capability of the murine leukemia virus Env protein, J. Virol. 68, 1773-1781
20. Kasahara, N., Dozy, A.M. and Kan, Y.W. (1994) Tissue-specific targeting of retroviral vectors through ligand-receptor interactions, Science 266, 1373-1376
21. Han, X., Kasahara, N. and Kan, Y.W. (1995) Ligand-directed retroviral targeting of human breast cancer cells, Proc. Natl. Acad. Sci. U. S. A. 92, 9747-9751
22. Matano, T. et al. (1995) Targeted infection of a retrovirus bearing a CD4-Env chimera into human cells expressing human immunodeficiency virus type 1, J. Gen. Virol. 76, 3165-3169
23. Kabat, D. (1995) Targeting retroviral vectors to specific cells, Science 269, 417
24. Chu, T-H. and Dornburg, R. (1997) Toward highly efficient cell-type-specific gene transfer with retroviral vectors displaying single-chain antibodies, J. Virol. 71, 720-725
25. Chu, T-H. and Dornburg, R. (1995) Retroviral vector particles displaying the antigen-binding site of an antibody enable cell-type-specific gene transfer, J. Virol. 69, 2659-2663
26. Chu, T-H. et al. (1994) Cell targeting with retroviral vector particles containing antibody-envelope fusion proteins, Gene Ther. 1, 292-299
27. Schnierle, B. et al. (1996) Expression of chimeric envelope proteins in helper cell lines and integration into Moloney murine leukemia virus particles. Gene Ther. 3, 334-342
28. Russell, S., Hawkins, R. and Winter, G. (1993) Retroviral vectors displaying functional antibody fragments, Nucleic Acids Res. 21, 1081-1085
29. Somia, N., Zoppé, M. and Verma, I. (1995) Generation of targeted retroviral vectors by using single-chain variable fragment: an approach to in vivo gene delivery, Proc. Natl. Acad. Sci. U. S. A. 92, 7570-7574
30. Marin, M. et al. (1996) Targeted infection of human cells via major histocompatibility complex class I molecules by Moloney murine leukemia virus-derived viruses displaying single-chain antibody fragment-envelope fusion proteins, J. Virol. 70, 2957-2062
31. Ager, S. et al. (1996) Retroviral display of antibody fragments; interdomain spacing strongly influences vector infectivity, Hum. Gene Ther. 7, 2157-2164
32. Valsesia, W.S. et al. (1994) Modifications in the binding domain of avian retrovirus envelope protein to redirect the host range of retroviral vectors, J. Virol. 68, 4609-4619
33. Nilson, B. et al. (1996) Targeting of retroviral vectors through protease-substrate interactions, Gene Ther. 3, 280-286
34. Arthur, L. et al. (1992) Cellular proteins bound to immunodeficiency virus: implications for pathogenesis and vaccines, Science 258, 1935-1938
35. Young, J. et al. (1990) Efficient incorporation of human CD4 protein into avian leukosis virus particles, Science 250, 1421-1423
36. D'Souza, P. and Harden, V. (1996) Chemokines and HIV-1 second receptors, Nat. Med. 2, 1293-1300