Innate immune responses in hepatitis C virus infection

被引:65
|
作者
Li, Kui [1 ]
Lemon, Stanley M. [2 ,3 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Microbiol Immunol & Biochem, Memphis, TN 38163 USA
[2] Univ N Carolina, Div Infect Dis, Dept Med, Inflammatory Dis Inst, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
Interferon; RIG-I; Toll-like receptor; JaK-STAT pathway; Interferon-stimulated gene; Immune evasion; Hepatitis C virus; TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; PROTEIN-KINASE-R; ANTIVIRAL SIGNALING PROTEIN; INTERFERON-STIMULATED GENES; WEST NILE VIRUS; ENDOPLASMIC-RETICULUM STRESS; NONSTRUCTURAL 5A PROTEIN; NF-KAPPA-B; RIG-I;
D O I
10.1007/s00281-012-0332-x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatitis C virus (HCV) is a major causative agent of chronic hepatitis and hepatocellular carcinoma worldwide and thus poses a significant public health threat. A hallmark of HCV infection is the extraordinary ability of the virus to persist in a majority of infected people. Innate immune responses represent the front line of defense of the human body against HCV immediately after infection. They also play a crucial role in orchestrating subsequent HCV-specific adaptive immunity that is pivotal for viral clearance. Accumulating evidence suggests that the host has evolved multifaceted innate immune mechanisms to sense HCV infection and elicit defense responses, while HCV has developed elaborate strategies to circumvent many of these. Defining the interplay of HCV with host innate immunity reveals mechanistic insights into hepatitis C pathogenesis and informs approaches to therapy. In this review, we summarize recent advances in understanding innate immune responses to HCV infection, focusing on induction and effector mechanisms of the interferon antiviral response as well as the evasion strategies of HCV.
引用
收藏
页码:53 / 72
页数:20
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