Innate Antiviral Response: Role in HIV-1 Infection

被引:25
作者
Pitha, Paula M. [1 ,2 ,3 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD 21231 USA
[2] Johns Hopkins Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
来源
VIRUSES-BASEL | 2011年 / 3卷 / 07期
关键词
virus; HIV-1; interferon; IRF; innate immune response; INTERFERON REGULATORY FACTOR; VIRUS TYPE-1 INFECTION; NF-KAPPA-B; TOLL-LIKE RECEPTORS; RIG-I; TRANSCRIPTIONAL ACTIVITY; DENDRITIC CELLS; FACTOR FAMILY; ACCESSORY PROTEINS; UBIQUITIN LIGASE;
D O I
10.3390/v3071179
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As an early response to infection, cells induce a profile of the early inflammatory proteins including antiviral cytokines and chemokines. Two families of transcriptional factors play a major role in the transcriptional activation of the early inflammatory genes: The well-characterized family of NFkB factors and the family of interferon regulatory factors (IRF). The IRFs play a critical role in the induction of type I interferon (IFN) and chemokine genes, as well as genes mediating antiviral, antibacterial, and inflammatory responses. Type I IFNs represent critical components of innate antiviral immunity. These proteins not only exert direct antiviral effects, but also induce maturation of dendritic cells (DC), and enhance functions of NK, T and B cells, and macrophages. This review will summarize the current knowledge of the mechanisms leading to the innate antiviral response with a focus on its role in the regulation of HIV-1 infection and pathogenicity. We would like this review to be both historical and a future perspective.
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页码:1179 / 1203
页数:25
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