Evasion of adaptive and innate immune response mechanisms by γ-herpesviruses

被引:21
|
作者
Feng, Pinghui [1 ]
Moses, Ashlee [2 ]
Frueh, Klaus [2 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90089 USA
[2] Oregon Hlth & Sci Univ, Vaccine & Gene Therapy Inst, Beaverton, OR 97006 USA
关键词
SARCOMA-ASSOCIATED-HERPESVIRUS; EPSTEIN-BARR-VIRUS; NF-KAPPA-B; RHESUS MACAQUE RHADINOVIRUS; MURINE GAMMAHERPESVIRUS 68; INTERFERON REGULATORY FACTORS; PRIMARY EFFUSION LYMPHOMA; K7 PROTEIN TARGETS; T-CELL IMMUNITY; HLA-CLASS-I;
D O I
10.1016/j.coviro.2013.05.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
gamma-Herpesviral immune evasion mechanisms are optimized to support the acute, lytic and the longterm, latent phase of infection. During acute infection, specific immune modulatory proteins limit, but also exploit, the antiviral activities of cell intrinsic innate immune responses as well as those of innate and adaptive immune cells. During latent infection, a restricted gene expression program limits immune targeting and cis-acting mechanisms to reduce the antigen presentation as well as antigenicity of latency-associated proteins. Here, we will review recent progress in our understanding of gamma-herpesviral immune evasion strategies.
引用
收藏
页码:285 / 295
页数:11
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