CMV-encoded Fcγ receptors: modulators at the interface of innate and adaptive immunity

被引:46
|
作者
Corrales-Aguilar, Eugenia [1 ]
Hoffmann, Katja [2 ]
Hengel, Hartmut [2 ]
机构
[1] Univ Costa Rica, Fac Microbiol, Virol CIET, San Jose 115012060, Costa Rica
[2] Univ Freiburg, Univ Med Ctr, Inst Virol, D-79104 Freiburg, Germany
关键词
Fc gamma Rs; Immune evasion; Cytomegalovirus; IgG; ADCC; HERPES-SIMPLEX-VIRUS; DEPENDENT CELLULAR CYTOTOXICITY; NATURAL-KILLER-CELLS; HUMAN CYTOMEGALOVIRUS GENOME; HUMAN NK CELLS; IMMUNOGLOBULIN-G; CRYSTAL-STRUCTURE; LATENT INFECTION; BINDING PROTEIN; DENDRITIC CELLS;
D O I
10.1007/s00281-014-0448-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The constant region of IgG antibodies mediates antiviral activities upon engaging host Fc gamma receptors (Fc gamma Rs) expressed by a variety of immune cells, such as antibody-dependent cellullar cytotoxcity (ADCC) executed by natural killer (NK)cells. Human cytomegalovirus (HCMV) is unique among viruses by encoding also an array of several Fc gamma-binding glycoproteins with cell surface disposition and concomitant incorporation into the virion. Evidence is increasing that the virus-encoded Fc gamma receptors differ in their Fc gamma binding mode but effectively operate as adversaries of host Fc gamma Rs since they are able to prevent IgG-mediated triggering of activating host Fc gamma Rs, i.e., Fc gamma RI, Fc gamma RIIA, and Fc gamma RIIIA. Here we discuss virus-encoded Fc gamma Rs as the first known HCMV inhibitors of IgG-mediated immunity which could account for the limited efficacy of HCMV hyperimmune globulin in clinical settings. A better understanding of their molecular mode of action opens up new perspectives for improving IgG therapies against HCMV disease.
引用
收藏
页码:627 / 640
页数:14
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