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PMID: 18272355 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

MDA5/RIG-I and virus recognition.

Current opinion in immunology ·Vol. 20 ·No. 1 ·2008-02-00 ·Pages 17-22

Takeuchi O, Akira S

Abstract

The innate immune system initially recognizes RNA virus infection and evokes antiviral responses by producing type I interferons (IFNs). Toll-like receptors (TLRs) and cytoplasmic retinoic acid-inducible gene I (RIG-I)-like helicases (RLHs) are the two major receptor systems for detecting RNA viruses. The RLH signaling pathways play essential roles in the recognition of RNA viruses in various cells, with the exception of plasmacytoid dendritic cells, which utilize TLRs for virus recognition. The route of infection determines the cell types responsible for type I IFN production. Recent studies have suggested that TLRs are critical for activation of adaptive immune responses against several virus infections, although it may be premature to draw such a conclusion for virus infections in general. In this review, we will discuss recent advances toward clarifying the signaling pathways activated by RLHs and TLRs.

MeSH Terms
Animals DEAD Box Protein 58 DEAD-box RNA Helicases/metabolism Immunity, Innate Interferon Type I/biosynthesis Interferon-Induced Helicase, IFIH1 Mice RNA Virus Infections/immunology Signal Transduction Toll-Like Receptors/metabolism
Chemicals
Interferon Type I Toll-Like Receptors Ddx58 protein, mouse Ifih1 protein, mouse DEAD Box Protein 58 DEAD-box RNA Helicases Interferon-Induced Helicase, IFIH1
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Takeuchi Osamu
Laboratory of Host Defense, WPI Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Akira Shizuo
Article Info
Journal
Current opinion in immunology
Abbr.
Curr Opin Immunol
ISSN
0952-7915
Published
2008-02-00
Epub
2008-00-12
Pages
17-22
Language
English
Region
England
NLM ID
8900118
Subset
IM
Grants
NIAID NIH HHS · P01 AI070167 · United States
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