Autophagy in HIV-Induced T Cell Death

被引:19
作者
Espert, Lucile [1 ]
Biard-Piechaczyk, Martine [1 ]
机构
[1] Univ Montpellier, Inst Biol, CPBS, CNRS UMR5236, F-34965 Montpellier 2, France
来源
AUTOPHAGY IN INFECTION AND IMMUNITY | 2009年 / 335卷
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; ACTIVE ANTIRETROVIRAL THERAPY; ENDOPLASMIC-RETICULUM STRESS; DEFICIENCY SYNDROME AIDS; HTLV-III/LAV ENVELOPE; PROTEASE INHIBITORS; ADAPTIVE IMMUNITY; IN-VIVO; TYPE-1; INFECTION; PLASMA-MEMBRANE;
D O I
10.1007/978-3-642-00302-8_15
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HIV infection leads to progressive CD4 T cell depletion, resulting in the development of AIDS. The mechanisms that trigger T cell death after HIV infection are still not fully understood, but a lot of data indicate that apoptosis of uninfected CD4 lymphocytes plays a major role. HIV directly modulates cell death using various strategies in which several viral proteins, in particular the envelope glycoproteins (Env), play an essential role. Importantly, Env, expressed on infected cells, triggers autophagy in uninfected CD4 T cells, leading to their apoptosis. Furthermore, HIV, like other viruses, has evolved strategies to inhibit this autophagic process in HIV-infected cells. This discovery further increases the level of complexity of the cellular processes involved in HIV-induced pathology. Interestingly, HIV protease inhibitors, currently used in highly active antiretroviral therapy (HAART), are able to induce autophagy in cancer cells, leading to a recent repositioning of these drugs as anticancer agents. This review presents an overview of the relationship between HIV, HAART, and autophagy.
引用
收藏
页码:307 / 321
页数:15
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