Unlocking HIV-1 Env: implications for antibody attack

被引:6
|
作者
Richard, Jonathan [1 ,2 ]
Ding, Shilei [1 ,2 ]
Finzi, Andres [1 ,2 ,3 ]
机构
[1] CHUM, Ctr Rech, 900 St Denis St, Montreal, PQ H2X 0A9, Canada
[2] Univ Montreal, Dept Microbiol Infectiol & Immunol, Montreal, PQ, Canada
[3] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
来源
AIDS RESEARCH AND THERAPY | 2017年 / 14卷
关键词
HIV-1; Env; gp120; ADCC; Nef; Vpu; BST-2; CD4; CD4-mimetics; RV144; CELL-MEDIATED CYTOTOXICITY; BROADLY NEUTRALIZING ANTIBODIES; GP120 ENVELOPE GLYCOPROTEIN; VACCINE EFFICACY TRIAL; HIV-1-INFECTED CELLS; ADCC; EPITOPES; BINDING; CONFORMATION; RESPONSES;
D O I
10.1186/s12981-017-0168-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Collective evidence supporting a role of Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC) in controlling HIV-1 transmission and disease progression emerged in the last few years. Non-neutralizing antibodies (nnAbs) recognizing conserved CD4-induced epitopes on Env and able to mediate potent ADCC against HIV-1-infected cells exposing Env in its CD4-bound conformation have been shown to be present in some RV144 vaccinees and most HIV-1-infected individuals. HIV-1 evolved sophisticated strategies to decrease exposure of this Env conformation by downregulating CD4 and by limiting the overall amount of cell-surface Env. In this review, we will summarize our contribution to this rapidly evolving field, discuss how structural properties of HIV-1 Env might have contributed to the modest efficacy of the RV144 trial and how we recently used this knowledge to develop new strategies aimed at sensitizing HIV-1-infected cells to ADCC mediated by easy to elicit nnAbs.
引用
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页数:5
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