Design and Production of Human Immunodeficiency Virus-Derived Vectors

Cell Biology, Four-Volume Set

Volumn 1, Issue , 2006, Pages 425-434

  Salmon, Patrick ^a   Trono, Didier ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84884861865     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-012164730-8/50053-8     Document Type: Chapter

References (16)

1. Berkowitz R., Ilves H., Lin W.Y., Eckert K., Coward A., Tamaki S., Veres G., Plavec I. Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virus. J. Virol. 2001, 75:3371-3382.
2. Brummelkamp T.R., Bernards R., Agami R. A system for stable expression of short interfering RNAs in mammalian cells. Science 2002, 296:550-553.
3. Curran M.A., Kaiser S.M., Achaso P.L., Nolan G.P. Efficient transduction of nondividing cells by optimized feline immunodeficiency virus vectors. Mol. Ther. 2000, 1:31-38.
4. Dull T., Zufferey R., Kelly M., Mandel R.J., Nguyen M., Trono D., Naldini L. A third-generation lentivirus vector with a conditional packaging system. J Virol. 1998, 72:8463-8471.
5. Follenzi A., Ailles L.E., Bakovic S., Geuna M., Naldini L. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nature Genet. 2000, 25:217-222.
6. Klages N., Zufferey R., Trono D. A stable system for the high-titer production of multiply attenuated lentiviral vectors. Mol. Ther. 2000, 2:170-176.
7. Lois C., Hong E.J., Pease S., Brown E.J., Baltimore D. Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors. Science 2002, 295:868-872.
8. Mitrophanous K., Yoon S., Rohll J., Patil D., Wilkes F., Kim V., Kingsman S., Kingsman A., Mazarakis N. Stable gene transfer to the nervous system using a non-primate lentiviral vector. Gene Ther. 1999, 6:1808-1818.
9. Naldini L., Blomer U., Galley P., Ory D., Mulligan R., Gage F.H., Verma I.M., Trono D. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996, 272:263-267.
10. Negre D., Mangeot P.E., Duisit G., Blanchard S., Vidalain P.O., Leissner P., Winter A.J., Rabourdin-Combe C., Mehtali M., Moullier P., Darlix J.L., Cosset F.L. Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells. Gene Ther. 2000, 7:1613-1623.
11. Salmon P., Kindler V., Ducrey O., Chapuis B., Zubler R.H., Trono D. High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with imporved lentiviral vectors. Blood 2000, 96:3392-3398.
12. Sandrin V., Boson B., Salmon P., Gay W., Negre D., Le Grand R., Trono D., Cosset F.L. Lentiviral vectors pseudotyped with a modified RD114 envelope glycoprotein show increased stability in sera and augmented transduction of primary lymphocytes and CD34+ cells derived from human and nonhuman primates. Blood 2002, 100:823-832.
13. Zennou V., Petit C., Guetard D., Nerhbass U., Montagnier L., Charneau P. HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 2000, 101:173-185.
14. Zufferey R., Donello J.E., Trono D., Hope T.J. Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J. Virol. 1999, 73:2886-2892.
15. Zufferey R., Dull T., Mandel R.J., Bukovsky A., Quiroz D., Naldini L., Trono D. Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J. Virol. 1998, 72:9873-9880.
16. Zufferey R., Nagy D., Mandel R.J., Naldini L., Trono D. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nature Biotechnol. 1997, 15:871-875.