Arriaga Maria E, Carr Jillian, Li Peng, Wang Bin, Saksena Nitin K
Retroviral Genetics Division, Center for Virus Research, Westmead Millennium Institute, Westmead Hospital, The University of Sydney, Sydney, Australia.
Curr HIV Res. 2006 Oct;4(4):401-9. doi: 10.2174/157016206778560063.
A variety of mechanisms of innate immunity that protect organisms from retroviral infections, including HIV, are known. Lentiviruses express viral infectivity factor (Vif) protein that has the ability to counter antiviral activity exhibited by the recently discovered host cytidine deaminases APOBEC3G and 3F. Although these host factors are present in diverse mammalian species and have been shown to act against various organisms, their importance in HIV infection has been highlighted because of their suggested activities against HIV in vivo and the strong conservation of the HIV vif gene encoding the Vif protein capable of countering this innate activity. The main purpose of this review is to provide a detailed overview on HIV-specific interaction of APOBEC3 subfamily of proteins and discuss its potential role in HIV pathogenesis.
已知多种先天性免疫机制可保护生物体免受包括HIV在内的逆转录病毒感染。慢病毒表达病毒感染因子(Vif)蛋白,该蛋白能够对抗最近发现的宿主胞苷脱氨酶APOBEC3G和3F所表现出的抗病毒活性。尽管这些宿主因子存在于多种哺乳动物物种中,并已显示出对各种生物体起作用,但其在HIV感染中的重要性已得到凸显,因为它们在体内对HIV具有推测的活性,且编码能够对抗这种先天性活性的Vif蛋白的HIV vif基因具有很强的保守性。本综述的主要目的是详细概述APOBEC3蛋白亚家族与HIV的特异性相互作用,并讨论其在HIV发病机制中的潜在作用。