Approaches for generating recombinant adenovirus vectors

被引:41
作者
Mizuguchi, H
Kay, MA
Hayakawa, T
机构
[1] Natl Inst Hlth Sci, Div Biol Chem & Biol, Tokyo 1588501, Japan
[2] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
gene therapy; adenovirus vector; tetracycline; gene regulation; fiber; targeting;
D O I
10.1016/S0169-409X(01)00215-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Various methods have been developed to facilitate the generation of recombinant adenovirus vectors, and three commercially available methods have been most widely used: the homologous recombination method in E1-complement cell lines, the homologous recombination method in bacteria, and an in vitro ligation method based on simple routine plasmid construction. These methods can insert foreign genes not only into the E1 deletion region, but also into the E3 deletion region, thereby permitting the construction of a binary transgene expression system in which heterologous genes can be inserted into both the El and E3 regions. By modifying the latter two methods, fiber-mutant adenovirus vectors can be also constructed in order to modify vector tropism. In this paper, we review recent advances in the construction of first generation adenovirus vectors and fiber-modified adenovirus vectors. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:165 / 176
页数:12
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