Interferon lambda: opportunities, risks, and uncertainties in the fight against HCV

被引:21
作者
Laidlaw, Stephen M. [1 ]
Dustin, Lynn B. [1 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford OX1 3SY, England
基金
美国国家卫生研究院;
关键词
innate immunity; interferon lambda; hepatitis C virus; hepatocyte; chronic infection; HEPATITIS-C VIRUS; GENOME-WIDE ASSOCIATION; INNATE IMMUNE-RESPONSE; IFN-LAMBDA; GENETIC-VARIATION; STIMULATED GENES; LIFE-CYCLE; SPONTANEOUS CLEARANCE; SIGNAL-TRANSDUCTION; ANTIVIRAL ACTIVITY;
D O I
10.3389/fimmu.2014.00545
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate immunity is key to the fight against the daily onslaught from viruses that our bodies are subjected to. Essential to this response are the interferons (IFNs) that prime our cells to block viral pathogens. Recent evidence suggests that the Type III (lambda) IFNs are intimately associated with the immune response to hepatitis C virus (HCV) infection. Genome-wide association studies have identified polymorphisms within the IFN-lambda gene locus that correlate with response to IFN alpha-based antiviral therapy and with spontaneous clearance of HCV infection. The mechanisms for these correlations are incompletely understood. Restricted expression of the IFN-lambda receptor, and the ability of IFN-lambda to induce IFN-stimulated genes in HCV-infected cells, suggest potential roles for IFN-lambda in HCV therapy even in this era of directly acting antivirals. This review summarizes our current understanding of the IFN-lambda family and the role of IFNs in the natural history of HCV infection.
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页数:10
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