Antibody-dependent cellular cytotoxicity in HIV infection

被引:0
|
作者
Forthal, Donald N. [1 ,2 ]
Finzi, Andres [3 ,4 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Med, Div Infect Dis, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Sch Biol Sci, Dept Mol Biol & Biochem, Irvine, CA 92717 USA
[3] Univ Montreal, Dept Microbiol Infect Dis & Immunol, Ctr Rech CHUM, Montreal, PQ, Canada
[4] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
关键词
antibody-dependent cellular cytotoxicity; CD4; Fc receptor; HIV; natural killer cell; phagocytosis; simian immunodeficiency virus; simian/human immunodeficiency virus; HUMAN-IMMUNODEFICIENCY-VIRUS; MUCOSAL SHIV CHALLENGE; NATURAL-KILLER-CELLS; NEUTRALIZING MONOCLONAL-ANTIBODIES; HIV-1/SIV CHIMERIC VIRUS; NEONATAL RHESUS MACAQUES; PRIMARY T-CELLS; PBL-SCID MICE; MEDIATED CYTOTOXICITY; IN-VITRO;
D O I
10.1097/QAD.00000000000002011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interactions between the Fc segment of IgG and its receptors (Fc gamma Rs) found on cells such as natural killer cells, monocytes, macrophages and neutrophils can potentially mediate antiviral effects in the setting of HIV and related infections. We review the potential role of Fc gamma R interactions in HIV, SIV and SHIV infections, with an emphasis on antibody dependent cellular cytotoxicity (ADCC). Notably, these viruses employ various strategies, including CD4 down-regulation and BST-2/tetherin antagonism to limit the effect of ADCC. Although correlative data suggest that ADCC participates in both protection and control of established infection, there is little direct evidence in support of either role. Direct evidence does, however, implicate an Fc gamma R-dependent function in augmenting the beneficial in-vivo activity of neutralizing antibodies. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:2439 / 2451
页数:13
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