Lentiviral vectors

被引:0
|
作者
P. V. Spirin
A. E. Vilgelm
V. S. Prassolov
机构
[1] Russian Academy of Sciences,Engelhardt Institute of Molecular Biology
来源
Molecular Biology | 2008年 / 42卷
关键词
gene transfer; gene expression; retroviruses; lentiviruses; human immunodeficiency virus type 1; lentiviral vectors; gene therapy;
D O I
暂无
中图分类号
学科分类号
摘要
The delivery of genetic material to mammalian cells is of great importance for modern fundamental biology, biomedicine, biotechnology, agriculture, and veterinary medicine. The development of new efficient techniques of gene transfer to human cells led to the advent of gene therapy, a novel approach to treating severe metabolic disorders, some viral infections (including HIV infection), autoimmune diseases, and genetic defects causing cancer. The review considers the main principles of constructing gene transfer and expression systems based on lentiviruses, a powerful tool for human gene therapy and transgenic research, with a special focus on the genome structure and life cycle of lentiviruses and the design and safety of lentiviral vector systems.
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页码:814 / 825
页数:11
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