Understudied Factors Influencing Fc-Mediated Immune Responses against Viral Infections

被引:14
|
作者
Anand, Sai Priya [1 ,2 ]
Finzi, Andres [1 ,2 ,3 ]
机构
[1] CHUM, Ctr Rech, Montreal, PQ H2X 0A9, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
[3] Univ Montreal, Dept Microbiol Infectiol & Immunol, Montreal, PQ H2X 0A9, Canada
关键词
antibodies; Fc-mediated effector functions; ADCC; ADCP; ADCML; viruses; DEPENDENT CELLULAR CYTOTOXICITY; HIV-1 ENVELOPE GLYCOPROTEIN; GP120 INNER DOMAIN; EBOLA-VIRUS GLYCOPROTEIN; MUCOSAL SHIV CHALLENGE; MONOCLONAL-ANTIBODIES; ANTI-HIV-1; ANTIBODIES; HUMAN IGG1; NONNEUTRALIZING ANTIBODIES; EFFECTOR FUNCTION;
D O I
10.3390/vaccines7030103
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibodies play a crucial role in host defense against viruses, both by preventing infection and by controlling viral replication. Besides their capacity to neutralize viruses, antibodies also exert their antiviral effects by crystallizable fragment (Fc)-mediated effector mechanisms. This involves a bridge between innate and adaptive immune systems, wherein antibodies form immune complexes that drive numerous innate immune effector functions, including antibody-dependent cellular cytotoxicity, antibody-dependent complement-mediated lysis, and antibody-dependent phagocytosis. Here, we review certain mechanisms that modulate these antibody-mediated effector functions against virally infected cells, such as viral glycoprotein shedding, viral glycoprotein internalization, antibody cooperativity, and antibody glycosylation. These mechanisms can either protect viral replication or enhance infected cell clearance. Here we discuss the importance of these understudied factors in modulating Fc-mediated effector functions.
引用
收藏
页数:14
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