Innate Antiviral Defenses Independent of Inducible IFNα/β Production

被引:22
作者
Paludan, Soren R. [1 ,2 ]
机构
[1] Univ Aarhus, Dept Biomed, Aarhus, Denmark
[2] Univ Aarhus, Aarhus Res Ctr Innate Immunol, Aarhus, Denmark
基金
英国医学研究理事会;
关键词
PLASMACYTOID DENDRITIC CELLS; HERPES-SIMPLEX ENCEPHALITIS; INTERFERON-STIMULATED GENES; AICARDI-GOUTIERES SYNDROME; DOUBLE-STRANDED-RNA; I INTERFERON; POSITIVE FEEDBACK; TLR3; DEFICIENCY; DNA SENSOR; KAPPA-B;
D O I
10.1016/j.it.2016.06.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The type I interferons (IFNs) (IFN alpha and IFN beta) not only have potent antiviral activities, but also have pathological functions if produced at high levels or over a long time. Recent articles have described antiviral immune mechanisms that are activated in response to virus infection at epithelial surfaces independently of IFN alpha and IFN beta. This may allow the host to exert rapid local antiviral activity and only induce a full-blown, and potentially pathological, type I IFN response in situations where stronger protective immunity is needed. Here, I describe the emerging understanding of early antiviral defenses, which are independent of type I IFN responses, and also discuss how this enables tissues to exert rapid antiviral activities and to limit type I IFN production.
引用
收藏
页码:588 / 596
页数:9
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