Production and concentration of pseudotyped HIV-1-based gene transfer vectors

Gene Therapy

Volumn 7, Issue 11, 2000, Pages 910-913

  Reiser, J ^a,b  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^b LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Gene therapy; Lentiviral vectors; Pseudotypes

Indexed keywords

VIRUS ENVELOPE PROTEIN; VIRUS GLYCOPROTEIN; VIRUS VECTOR;

ARTICLE; GENE TRANSFER; GENETIC TRANSFECTION; HUMAN IMMUNODEFICIENCY VIRUS 1; MOLONEY LEUKEMIA ONCOVIRUS; PRIORITY JOURNAL; RABIES VIRUS; ULTRACENTRIFUGATION; ULTRAFILTRATION; VESICULAR STOMATITIS VIRUS;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; MOLONEY MURINE LEUKEMIA VIRUS; MURINAE; ONCOVIRINAE; RABIES VIRUS; VESICULAR STOMATITIS VIRUS;

EID: 0034083194     PISSN: 09697128     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.gt.3301188     Document Type: Article

References (12)

1. Naldini L. Lentiviruses as gene transfer agents for delivery to non-dividing cells. Curr Opin Biotechnol 1998; 9: 457-463.
2. Naldini L, Verma IM. Lentiviral vectors. In: Friedmann T (ed). The Development of Human Gene Therapy. Cold Spring Harbor Laboratory Press: Cold Spring Harbor, 1999, pp 47-60.
3. Naldini L et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996; 272: 263-267.
4. 2 accumulation by a mechanism which differs from DNA damage checkpoint control. J Virol 1996; 70: 2324-2331.
5. Burns JC et al. 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 1993; 90: 8033-8037.
6. Reiser J et al. Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc Natl Acad Sci USA 1996; 93: 15266-15271.
7. Mochizuki H et al. High-titer immunodeficiency type 1-based vector systems for gene delivery into nondividing cells. J Virol 1998; 72: 8873-8883.
8. Cosset FL et al. High-titer packaging cells producing recombinant retroviruses resistant to human serum. J Virol 1995; 69: 7430-7436.
9. Chu TH, Dornburg R. Toward highly efficient cell-type-specific gene transfer with retroviral vectors displaying single-chain antibodies. J Virol 1997; 71: 720-725.
10. DuBridge RB et al. Analysis of mutation in human cells by using an Epstein-Barr virus shuttle system. Mol Cell Biol 1987; 7: 379-387.
11. Pear WS, Nolan GP, Scott ML, Baltimore D. Production of high-titer helper-free retroviruses by transient transfection. Proc Natl Acad Sci USA 1993; 90: 8392-8396.
12. Charneau P et al. HIV-1 reverse transcription. A termination step at the center of the genome. J Mol Biol 1994; 241: 651-662.