期刊
FRONTIERS IN IMMUNOLOGY
卷 7, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2016.00628
关键词
hepatitis C; IFN-lambda 3; IFN-lambda 4; liver; SNP; HCV clearance; SVR
类别
资金
- Canadian Institutes of Health Research (CIHR) [MOP-133680]
- Alberta Innovates Health Solutions
- Canadian Liver Foundation
- American Liver Foundation
- Fonds de Recherche du Quebec-Sante (FRQS)
- Canadian Network on Hepatitis C (CanHepC)
- FRQS
- Alberta Innovates [201201140] Funding Source: researchfish
The interferon (IFN)-lambda family of type III cytokines includes the closely related interleukin (IL)-28A (IFN-lambda 2), IL-28B (IFN-lambda 3), and IL-29 (IFN-lambda 1). They signal through the Janus kinases (JAK)-signal transducers and activators of transcription pathway and promote an antiviral state by the induction of expression of several interferon-stimulated genes (ISGs). Contrary to type I IFNs, the effect of IFN-lambda cytokines is largely limited to epithelial cells due to the restricted pattern of expression of their specific receptor. Several genome-wide association studies have established a strong correlation between polymorphism in the region of IL-28B gene (encoding for IFN-lambda 3) and both spontaneous and therapeutic IFN-mediated clearance of hepatitis C virus (HCV) infection, but the mechanism(s) underlying this enhanced viral clearance are not fully understood. IFN-lambda 3 directly inhibits HCV replication, and in vitro studies suggest that polymorphism in the IFN-lambda 3 and its recently identified overlapping IFN-lambda 4 govern the pattern of ISGs induced upon HCV infection of hepatocytes. IFN-lambda can also be produced by dendritic cells, and apart from its antiviral action on hepatocytes, it can regulate the inflammatory response of monocytes/macrophages, thus acting at the interface between innate and adaptive immunity. Here, we review the current state of knowledge about the role of IFN-lambda cytokines in mediating and regulating the immune response during acute and chronic HCV infections.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据