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Manipulation of the nuclear factor-κB pathway and the innate immune response by viruses
被引:213
作者:
Hiscott, J.
Nguyen, T-L A.
Arguello, M.
Nakhaei, P.
Paz, S.
机构:
[1] McGill Univ, Lady Davis Inst Med Res, Terry Fox Mol Oncol Grp, Montreal, PQ, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] McGill Univ, Dept Med & Oncol, Montreal, PQ, Canada
来源:
基金:
加拿大健康研究院;
关键词:
NF-kappaB;
innate immunity;
interferons;
viral evasion;
Toll-like receptors;
D O I:
10.1038/sj.onc.1209941
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Viral and microbial constituents contain specific motifs or pathogen-associated molecular patterns (PAMPs) that are recognized by cell surface-and endosome-associated Toll-like receptors (TLRs). In addition, intracellular viral double-stranded RNA is detected by two recently characterized DExD/H box RNA helicases, RIG-I and Mda-5. Both TLR-dependent and -independent pathways engage the I kappa B kinase (IKK) complex and related kinases TBK-1 and IKK epsilon. Activation of the nuclear factor kappa B (NF-kappa B) and interferon regulatory factor (IRF) transcription factor pathways are essential immediate early steps of immune activation; as a result, both pathways represent prime candidates for viral interference. Many viruses have developed strategies to manipulate NF-kappa B signaling through the use of multifunctional viral proteins that target the host innate immune response pathways. This review discusses three rapidly evolving areas of research on viral pathogenesis: the recognition and signaling in response to virus infection through TLR-dependent and -independent mechanisms, the involvement of NF-kappa B in the host innate immune response and the multitude of strategies used by different viruses to short circuit the NF-kappa B pathway.
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页码:6844 / 6867
页数:24
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