Viral vectors: from virology to transgene expression

被引:250
作者
Bouard, D.
Alazard-Dany, N.
Cosset, F-L [1 ]
机构
[1] ENS Lyon, INSERM, Human Virol Dept, U758, F-69007 Lyon, France
关键词
viral vectors; gene therapy; AAV; Ad; HSV; lentivectors; pseudotyping; cell targeting; transcriptional targeting; vectors production; EFFICIENT GENE-TRANSFER; RECOMBINANT ADENOASSOCIATED VIRUS; ENGINEERED LENTIVIRAL VECTORS; DEPENDENT ADENOVIRAL VECTORS; TRANSDUCE AIRWAY EPITHELIA; SITE-SPECIFIC INTEGRATION; HSV-1 AMPLICON VECTORS; THYMIDINE KINASE GENE; RETROVIRAL VECTORS; IN-VIVO;
D O I
10.1038/bjp.2008.349
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the late 1970s, it was predicted that gene therapy would be applied to humans within a decade. However, despite some success, gene therapy has still not become a routine practise in medicine. In this review, we will examine the problems, both experimental and clinical, associated with the use of viral material for transgenic insertion. We shall also discuss the development of viral vectors involving the most important vector types derived from retroviruses, adenoviruses, herpes simplex viruses and adeno-associated viruses.
引用
收藏
页码:153 / 165
页数:13
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