Intrinsic host restrictions to HIV-1 and mechanisms of viral escape

被引:211
|
作者
Simon, Viviana [1 ]
Bloch, Nicolin [2 ]
Landau, Nathaniel R. [2 ]
机构
[1] Icahn Sch Med Mt Sinai, Global Hlth & Emerging Pathogens Inst, Dept Microbiol, New York, NY 10029 USA
[2] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; AICARDI-GOUTIERES SYNDROME; ANCIENT ADAPTIVE EVOLUTION; TYPE-1 VPU PROTEIN; CBF-BETA; INHIBITS HIV-1; PARTICLE RELEASE; SAMHD1; RESTRICTS; ANTIRETROVIRAL ACTIVITY; PRIMATE LENTIVIRUSES;
D O I
10.1038/ni.3156
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To replicate in their hosts, viruses have to navigate the complexities of the mammalian cell, co-opting mechanisms of cellular physiology while defeating restriction factors that are dedicated to halting their progression. Primate lentiviruses devote a relatively large portion of their coding capacity to counteracting restriction factors by encoding accessory proteins dedicated to neutralizing the antiviral function of these intracellular inhibitors. Research into the roles of the accessory proteins has revealed the existence of previously undetected intrinsic defenses, provided insight into the evolution of primate lentiviruses as they adapt to new species and uncovered new targets for the development of therapeutics. This Review discusses the biology of the restriction factors APOBEC3, SAMHD1 and tetherin and the viral accessory proteins that counteract them.
引用
收藏
页码:546 / 553
页数:8
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