The Journal of Gene Medicine · 2005 · 77 citations · 42 references
Life SciencesBiotechnologyGene ExpressionMolecular VirologyVirologyVector ProductionViral Gene ExpressionConstitutive Expression SystemsConstitutive Gene ExpressionLentiviral Vector ManufacturingLentiviral VectorsRetroviral Vector ManufacturingScale-up Of Vector ProductionStable Cell Line GenerationViral Vector Production
BACKGROUND: A stable packaging cell line facilitates large-scale lentivirus vector manufacture. However, it has been difficult to produce clinical-scale HIV-1-based lentiviral vectors using a packaging cell line, in part due to toxicity of packaging genes, and gene silencing that occurs during the long culture period necessary for sequential addition of packaging constructs. METHODS: To avoid these problems, we developed a three-level cascade gene regulation system designed to remove tetracycline transactivator (tTA) from cytomegalovirus immediate early promoter (CMV)-controlled expression to reduce cytotoxicity from constitutive expression of tTA and leaky expression of packaging genes. We also performed a one-step integration of the three packaging plasmids to shorten the culture time for clonal selection. RESULTS: Although leaky expression of p24 and vector production still occurred despite the three-level regulation system, little cytotoxicity was observed and producer cells could be expanded for large-scale production. Producer cells yielded remarkably stable vector production over a period greater than 11 days with the highest titer 3.5 x 10(7) transducing units (TU)/ml and p24 300 ng/ml, yielding 2.2 x 10(11) TU and 1.8 milligram (mg) p24 from one cell factory. No replication-competent lentivirus (RCL) was detected. Long-term analysis demonstrated that, although the cells are genetically stable, partial gene silencing occurs after 2-3 months in culture; however, the one-step construct integration allowed prolonged vector production before significant gene silencing. Concentrated vector resulted in 90% transduction in CD4+ lymphocytes at 20 TU per cell. CD34+ progenitor cells were transduced at 41-46% efficiency, and long-term initiating culture (LTC-IC) was transduced at 45-51%. CONCLUSIONS: These results demonstrate for the first time HIV-1-based lentiviral vector production on the large scale using a packaging cell line.
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David Garrick, Steven Fiering, David I. K. Martin et al. · Nature Genetics · 1998 · 897 citations
Negative effect of the transcriptional activator GAL4
Grace Gill, Mark Ptashne · Nature · 1988 · 683 citations
Regulation by HIV Rev depends upon recognition of splice sites
David Chang, Phillip A. Sharp · Cell · 1989 · 516 citations
Penny E. Shockett, Michael J. Difilippantonio, Nathan E. Hellman et al. · Proceedings of the National Academy of Sciences · 1995 · 380 citations