By Nancy Smyth Templeton
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Additional info for Gene and Cell Therapy: Therapeutic Mechanisms and Strategies, Second Edition, Revised and Expanded
Proc. Natl. Acad. Sci. USA 1998; 95:7063–7068. Boerger AL, Snitkovsky S, Young JA. Retroviral vectors preloaded with a viral receptor–ligand bridge protein are targeted to specific cell types. Proc. Natl. Acad. Sci. USA 1999; 96: 9867–9872. Mothes W, Boerger AL, Narayan S, Cunningham JM, Young JA. Retroviral entry mediated by receptor priming and low pH triggering of an envelope glycoprotein. Cell 2000; 103: 679–689. Hatziioannou T, Vasesia-Wittmann S, Russell S, Cosset F-L. Incorporation of fowl plague virus hemagglutinin into murine leukemia virus particles and analysis of the infectivity of the pseudotyped retroviruses.
B. In Vitro Studies The methods outlined above have been used to make a large number of first-generation E1מ, E3 מadenoviral vectors. Among the most widely used are those that express readily monitored reporter genes such as ␤-galactosidase, luciferase, chloramphenicol acetyl transferase, and green fluorescent protein (34,35). As a control, viruses with the same promoterdriving expression of no transgene (AdNull) are used. Using the reporter gene Ad vectors, there are many studies examining the ease of gene transfer to different primary cells and cell lines.
118) showed this theory to be correct and further demonstrated that the expected selectivity is maintained in vivo. In this context, the vector Av1AFPTK1 [expressing thymidine kinase from herpes simplex virus (HSV-TK) from the AFP promoter] can prevent tumor growth in gancyclovir-treated nude mice implanted with a AFP-expressing tumor cell line but not in identical mice implanted with a control (non-AFP expressing) tumor cell line. In contrast, the vector Av1TK1, which expresses HSV-TK from the Rous sarcoma virus promoter, protects gancyclovir-treated nude mice regardless of which cell line is used to transduce the tumor.