RIG-I and Other RNA Sensors in Antiviral Immunity

被引:334
作者
Chow, Kwan T. [1 ]
Gale, Michael, Jr.
Loo, Yueh-Ming
机构
[1] Univ Washington, Ctr Innate Immun & Immune Dis, Seattle, WA 98109 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 36 | 2018年 / 36卷
关键词
RIG-I-like receptors; RLR; DExD/H box helicases; Toll-like receptors; TLR; RNA sensing; antiviral immunity; innate immune signaling; TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; PLASMACYTOID DENDRITIC CELLS; E3 UBIQUITIN LIGASE; ACID-SENSING TLRS; INDUCIBLE GENE-I; NUCLEIC-ACID; STRUCTURAL BASIS; ENDOPLASMIC-RETICULUM; MESSENGER-RNA;
D O I
10.1146/annurev-immunol-042617-053309
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Pattern recognition receptors (PRRs) survey intra- and extracellular spaces for pathogen-associated molecular patterns (PAMPs) within microbial products of infection. Recognition and binding to cognate PAMP ligand by specific PRRs initiates signaling cascades that culminate in a coordinated intracellular innate immune response designed to control infection. In particular, our immune system has evolved specialized PRRs to discriminate viral nucleic acid from host. These are critical sensors of viral RNA to trigger innate immunity in the vertebrate host. Different families of PRRs of virus infection have been defined and reveal a diversity of PAMP specificity for wide viral pathogen coverage to recognize and extinguish virus infection. In this review, we discuss recent insights in pathogen recognition by the RIG-I-like receptors, related RNA helicases, Toll-like receptors, and other RNA sensor PRRs, to present emerging themes in innate immune signaling during virus infection.
引用
收藏
页码:667 / 694
页数:28
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