Interferon induction and function at the mucosal surface

被引:196
作者
Durbin, Russell K. [1 ]
Kotenko, Sergei V. [2 ]
Durbin, Joan E. [1 ]
机构
[1] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[2] Univ Med & Dent NJ, New Jersey Med Sch, Dept Biochem, Newark, NJ USA
关键词
interferon; influenza A virus; respiratory syncytial virus; rotavirus; IFN induction; Stat signaling; RESPIRATORY-SYNCYTIAL-VIRUS; INFLUENZA-A-VIRUS; NF-KAPPA-B; DOUBLE-STRANDED-RNA; IFN-LAMBDA-S; PHOSPHORYLATION-ACETYLATION SWITCH; PROTEIN-TYROSINE-PHOSPHATASE; PLASMACYTOID DENDRITIC CELLS; STIMULATED GENE-EXPRESSION; EPSILON IKK-EPSILON;
D O I
10.1111/imr.12101
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferons (IFNs) are produced in response to virus infection and induce an antiviral state in virtually all cell types. In addition to upregulating the transcription of genes that inhibit virus replication, type I (or -/) IFNs also act to orchestrate the adaptive immune response to virus infection. Recently a new family of antiviral cytokines, the type III (or -) IFNs, has been identified that activate the same antiviral pathways via a distinct receptor. Although the identical transcription factor, IFN-stimulated gene factor 3 is activated by either IFN-/ or IFN- signaling, differences in the induction and action of these two cytokine families are beginning to be appreciated. In this article, we review this emerging body of literature on the differing roles these cytokines play in host defense of the mucosal surface. Although many viruses enter the body through the respiratory and gastrointestinal tracts, we have focused the discussion on influenza A virus, respiratory syncytial virus, and rotavirus, three ubiquitous human pathogens that target the epithelial lining and are associated with a major disease burden.
引用
收藏
页码:25 / 39
页数:15
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