| 1. |
DuBridge, R. B., Tang, P., Hsia, H. C., Leong, P. M., Miller, J. H., and Calos, M. P. (1987) Analysis of mutation in human
cells by using an Epstein-Barr virus shuttle system. Mol. Cell Biol.
7, 379–387.
|
| |
| 2. |
Soneoka, Y., Cannon, P. M., Ramsdale, E. E., et al. (1995) A transient three-plasmid expression system for the production
of high titer retroviral vectors. Nucleic Acids Res.
23, 628–633.
|
| |
| 3. |
Gluzman, Y. (1981) SV40-transformed simian cells support the replication of early SV40 mutants. Cell
23, 175–182.
|
| |
| 4. |
Stratton, M. R., Reeves, B. R., and Cooper, C. S. (1989) Misidentified cell. Nature
337, 311–312.
|
| |
| 5. |
Page, K. A., Landau, N. R., and Littman, D. R. (1990) Construction and use of a human immunodeficiency virus vector for analysis
of virus infectivity. J. Virol.
64, 5270–5276.
|
| |
| 6. |
Reiser, J., Harmison, G., Kluepfel-Stahl, S., Brady, R. O., Karlsson, S., and Schubert, M. (1996) Transduction of nondividing
cells using pseudotyped defective high-titer HIV type 1 particles. Proc. Natl. Acad. Sci. USA
93, 15,266–15,271.
|
| |
| 7. |
Chang, L. J., Urlacher, V., Iwakuma, T., Cui, Y., and Zucali, J. (1999) Efficacy and safety analyses of a recombinant human
immunodeficiency virus type 1 derived vector system. Gene Ther.
6, 715–728.
|
| |
| 8. |
Landau, N. R., Page, K. A., and Littman, D. R. (1991) Pseudotyping with human T-cell leukemia virus type I broadens the human
immunodeficiency virus host range. J. Virol.
65, 162–169.
|
| |
| 9. |
Akkina, R. K., Walton, R. M., Chen, M. L., Li, Q. X., Planelles, V., and Chen, I. S. (1996) High-efficiency gene transfer
into CD34+ cells with a human immunode-ficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis
virus envelope glycoprotein G. J. Virol.
70, 2581–2585.
|
| |
| 10. |
Naldini, L., Blömer, U., Gallay, P., et al. (1996) In vivo gene delivery and stable transduction of nondividing cells by a
lentiviral vector. Science
272, 263–267.
|
| |
| 11. |
Mochizuki, H., Schwartz, J. P., Tanaka, K., Brady, R. O., and Reiser, J. (1998) High-titer human immunodeficiency virus type
1-based vector systems for gene delivery into nondividing cells. J. Virol.
72, 8873–8883.
|
| |
| 12. |
Dull, T., Zufferey, R., Kelly, M., et al. (1998) A third-generation lentivirus vector with a conditional packaging system.
J. Virol.
72, 8463–8471.
|
| |
| 13. |
Hanawa, H., Kelly, P. F., Nathwani, A. C., et al. (2002) Comparison of various envelope proteins for their ability to pseudotype
lentiviral vectors and transduce primitive hematopoietic cells from human blood. Mol. Ther.
5, 242–251.
|
| |
| 14. |
Carroll, R., Lin, J. T., Dacquel, E. J., Mosca, J. D., Burke, D. S., and St Louis, D. C. (1994) A human immunodeficiency virus
type 1 (HIV-1)-based retroviral vector system utilizing stable HIV-1 packaging cell lines. J. Virol.
68, 6047–6051.
|
| |
| 15. |
Corbeau, P., Kraus, G., and Wong-Staal, F. (1996) Efficient gene transfer by a human immunodeficiency virus type 1 (HIV-1)-derived
vector utilizing a stable HIV packaging cell line. Proc. Natl. Acad. Sci. USA
93, 14,070–14,075.
|
| |
| 16. |
Kaplan, A. H. and Swanstrom, R. (1991) The HIV-1 gag precursor is processed via two pathways: implications for cytotoxicity.
Biomed. Biochim. Acta
50, 647–653.
|
| |
| 17. |
Rogel, M. E., Wu, L. I., and Emerman, M. (1995) The human immunodeficiency virus type 1 vpr gene prevents cell proliferation
during chronic infection. J. Virol.
69, 882–888.
|
| |
| 18. |
Li, Y., Drone, C., Sat, E., and Ghosh, H. P. (1993) Mutational analysis of the vesicular stomatitis virus glycoprotein G for
membrane fusion domains. J. Virol.
67, 4070–4077.
|
| |
| 19. |
Gossen, M. and Bujard, H. (1992) Tight control of gene expression in mammalian cells by tetracycline-responsive promoters.
Proc. Natl. Acad. Sci. USA
89, 5547–5551.
|
| |
| 20. |
No, D., Yao, T. P., and Evans, R. M. (1996) Ecdysone-inducible gene expression in mammalian cells and transgenic mice. Proc. Natl. Acad. Sci. USA
93, 3346–3351.
|
| |
| 21. |
Yu, H., Rabson, A. B., Kaul, M., Ron, Y., and Dougherty, J. P. (1996) Inducible human immunodeficiency virus type 1 packaging
cell lines. J. Virol.
70, 4530–4537.
|
| |
| 22. |
Kaul, M., Yu, H., Ron, Y., and Dougherty, J. P. (1998) Regulated lentiviral packaging cell line devoid of most viral cis-acting
sequences. Virology
249, 167–174.
|
| |
| 23. |
Kafri, T., van Praag, H., Ouyang, L., Gage, F. H., and Verma, I. M. (1999) A packaging cell line for lentivirus vectors. J. Virol.
73, 576–584.
|
| |
| 24. |
Klages, N., Zufferey, R., and Trono, D. (2000) A stable system for the high-titer production of multiply attenuated lentiviral
vectors. Mol. Ther.
2, 170–176.
|
| |
| 25. |
Xu, K., Ma, H., McCown, T. J., Verma, I. M., and Kafri, T. (2001) Generation of a stable cell line producing high-titer self-inactivating
lentiviral vectors. Mol. Ther.
3, 97–104.
|
| |
| 26. |
Pacchia, A. L., Adelson, M. E., Kaul, M., Ron, Y., and Dougherty, J. P. (2001) An inducible packaging cell system for safe,
efficient lentiviral vector production in the absence of HIV-1 accessory proteins. Virology
282, 77–86.
|
| |
| 27. |
Farson, D., Witt, R., McGuinness, R., et al. (2001) A new-generation stable inducible packaging cell line for lentiviral vectors.
Hum. Gene Ther.
12, 981–997.
|
| |
| 28. |
Sparacio, S., Pfeiffer, T., Schaal, H., and Bosch, V. (2001) Generation of a flexible cell line with regulatable, high-level
expression of HIV Gag/Pol particles capable of packaging HIV-derived vectors. Mol. Ther.
3, 602–612.
|
| |
| 29. |
Canivet, M., Hoffman, A. D., Hardy, D., Sernatinger, J., and Levy, J. A. (1990) Replication of HIV-1 in a wide variety of
animal cells following phenotypic mixing with murine retroviruses. Virology
178, 543–551.
|
| |
| 30. |
Lusso, P., di Marzo Veronese, F., Ensoli, B., et al. (1990) Expanded HIV-1 cellular tropism by phenotypic mixing with murine
endogenous retroviruses. Science
247, 848–852.
|
| |
| 31. |
Chesebro, B., Wehrly, K., and Maury, W. (1990) Differential expression in human and mouse cells of human immunodeficiency
virus pseudotyped by murine retroviruses. J. Virol.
64, 4553–4557.
|
| |
| 32. |
Spector, D. H., Wade, E., Wright, D. A., et al. (1990) Human immunodeficiency virus pseudotypes with expanded cellular and
species tropism. J. Virol.
64, 2298–2308.
|
| |
| 33. |
Zhu, Z. H., Chen, S. S., and Huang, A. S. (1990) Phenotypic mixing between human immunodeficiency virus and vesicular stomatitis
virus or herpes simplex virus. J. Acquir. Immune Defic. Syndr.
3, 215–219.
|
| |
| 34. |
Landau, N. R. and Littman, D. R. (1992) Packaging system for rapid production of murine leukemia virus vectors with variable
tropism. J. Virol.
66, 5110–5113.
|
| |
| 35. |
Sutton, R. E. and Littman, D. R. (1996) Broad host range of human T-cell leukemia virus type 1 demonstrated with an improved
pseudotyping system. J. Virol.
70, 7322–7326.
|
| |
| 36. |
Stitz, J., Buchholz, C. J., Engelstadter, M., et al. (2000) Lentiviral vectors pseudotyped with envelope glycoproteins derived
from gibbon ape leukemia virus and murine leukemia virus 10A1. Virology
273, 16–20.
|
| |
| 37. |
Christodoulopoulos, I. and Cannon, P. M. (2001) Sequences in the cytoplasmic tail of the gibbon ape leukemia virus envelope
protein that prevent its incorporation into lentivirus vectors. J. Virol.
75, 4129–4138.
|
| |
| 38. |
Lewis, B. C., Chinnasamy, N., Morgan, R. A., and Varmus, H. E. (2001) Development of an avian leukosis-sarcoma virus subgroup
A pseudotyped lentiviral vector. J. Virol.
75, 9339–9344.
|
| |
| 39. |
Beyer, W. R., Westphal, M., Ostertag, W., and von Laer, D. (2002) Oncoretrovirus and lentivirus vectors pseudotyped with lymphocytic
choriomeningitis virus glycoprotein: generation, concentration, and broad host range. J. Virol.
76, 1488–1495.
|
| |
| 40. |
Kobinger, G. P., Weiner, D. J., Yu, Q. C., and Wilson, J. M. (2001) Filovirus-pseudotyped lentiviral vector can efficiently
and stably transduce airway epithelia in vivo. Nat. Biotechnol.
19, 225–230.
|
| |
| 41. |
Chan, S. Y., Speck, R. F., Ma, M. C., and Goldsmith, M. A. (2000) Distinct mechanisms of entry by envelope glycoproteins of
Marburg and Ebola (Zaire) viruses. J. Virol.
74, 4933–4937.
|
| |
| 42. |
Burns, J. C., Friedmann, T., Driever, W., Burrascano, M., and Yee, J. K. (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. USA
90, 8033–8037.
|
| |
| 43. |
Bartz, S. R. and Vodicka, M. A. (1997) Production of high-titer human immuno-deficiency virus type 1 pseudotyped with vesicular
stomatitis virus glycoprotein. Methods
12, 337–342.
|
| |
| 44. |
Reiser, J. (2000) Production and concentration of pseudotyped HIV-1-based gene transfer vectors. Gene Ther.
7, 910–913.
|
| |
| 45. |
VandenDriessche, T., Naldini, L., Collen, D., and Chuah, M. K. (2002) Oncoretroviral and lentiviral vector-mediated gene therapy.
Methods Enzymol.
346, 573–589.
|
| |
| 46. |
Stein, C. S. and Davidson, B. L. (2002) Gene transfer to the brain using feline immunodeficiency virus-based lentivirus vectors.
Methods Enzymol.
346, 433–454.
|
| |
| 47. |
Nomura, T., Yabe, T., Mochizuki, H., Reiser, J., Becerra, S. P., and Schwartz, J. P. (2001) Survival effects of pigment epithelium-derived
factor expressed by a lentiviral vector in rat cerebellar granule cells. Dev. Neurosci.
23, 145–152.
|
| |
| 48. |
Cui, Y., Golob, J., Kelleher, E., Ye, Z., Pardoll, D., and Cheng, L. (2002) Targeting transgene expression to antigen-presenting
cells derived from lentivirus-transduced engrafting human hematopoietic stem/progenitor cells. Blood
99, 399–408.
|
| |
| 49. |
Pham, L., Ye, H., Cosset, F. L., Russell, S. J., and Peng, K. W. (2001) Concentration of viral vectors by co-precipitation
with calcium phosphate. J. Gene Med.
3, 188–194.
|
| |
| 50. |
Zhang, B., Xia, H. Q., Cleghorn, G., Gobe, G., West, M., and Wei, M. Q. (2001) A highly efficient and consistent method for
harvesting large volumes of high-titre lentiviral vectors. Gene Ther.
8, 1745–1751.
|
| |
| 51. |
Scherr, M., Battmer, K., Blömer, U., et al. (2002) Lentiviral gene transfer into peripheral blood-derived CD34+ NOD/SCID-repopulating
cells. Blood
99, 709–712.
|
| |
| 52. |
Cosset, F. L., Takeuchi, Y., Battini, J. L., Weiss, R. A., and Collins, M. K. (1995) High-titer packaging cells producing
recombinant retroviruses resistant to human serum. J. Virol.
69, 7430–7436.
|
| |
| 53. |
Reiser, J., Lai, Z., Zhang, X. Y., and Brady, R. O. (2000) Development of multigene and regulated lentivirus vectors. J. Virol.
74, 10,589–10,599.
|
| |
| 54. |
Wu, X., Wakefield, J. K., Liu, H., Xiao, H., Kralovics, R., Prchal, J. T., and Kappes, J. C. (2000) Development of a novel
trans-lentiviral vector that affords predictable safety. Mol. Ther.
2, 47–55.
|
| |
| 55. |
Sakoda, T., Kasahara, N., Hamamori, Y., and Kedes, L. (1999) A high-titer lentiviral production system mediates efficient
transduction of differentiated cells including beating cardiac myocytes. J. Mol. Cell Cardiol.
31, 2037–2047.
|
| |
| 56. |
Higashikawa, F. and Chang, L. (2001) Kinetic analyses of stability of simple and complex retroviral vectors. Virology
280, 124–131.
|
| |