中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Ifn-lambda 4 desensitizes the response to ifn-alpha treatment in chronic hepatitis c through long-term induction of usp18

文献类型:期刊论文

作者Fan, Weiguo1; Xie, Shiqi1,5; Zhao, Xinhao1; Li, Nan1,2; Chang, Chong1; Li, Li1; Yu, Ge3; Chi, Xiumei3; Pan, Yu3; Niu, Junqi3
刊名Journal of general virology
出版日期2016-09-01
卷号97页码:2210-2220
ISSN号0022-1317
DOI10.1099/jgv.0.000522
通讯作者Niu, junqi(junqiniu@aliyun.com) ; Zhong, jin(jzhong@sibs.ac.cn) ; Sun, bing(bsun@sibs.ac.cn)
英文摘要The recently discovered interferon lambda 4 (ifn-lambda 4) is a new member of the human type iii interferons which could induce a strong antiviral effect through the jak-stat cascade. however, hepatitis c virus (hcv) patients who are capable of expressing ifn-lambda 4 usually have poor response to ifn-alpha treatment, and the mechanism behind this paradox remains unknown. here, we reported that ifn-lambda 4 desensitized ifn-alpha-stimulated jak-stat signalling. microarray analysis revealed that ifn-lambda 4 could induce ubiquitin specific peptidase 18 (usp18), a known inhibitor of the type i ifn signalling pathway, in a more sustained pattern compared with type i interferon induction. moreover, only hcv genotype 1b but not 2a replicon cells pretreated with ifn-lambda 4 had an attenuated response to type i ifn treatment, which might be due to the different level of usp18 expression. consistently, knockdown of usp18 in hcv genotype 1b-containing replicon cells reversed the resistance induced by ifn-lambda 4 and promoted viral clearance. finally, ifn-lambda 4 is also strongly associated with the poor response to ifn-alpha in a chinese hcv genotype 1b cohort. in conclusion, these data indicate that ifn-lambda 4 attenuates the response of hcv genotype 1b to ifn-alpha therapy and inhibits the jak-stat signalling pathway by inducing usp18 expression.
WOS关键词HUMAN-LEUKOCYTE INTERFERON ; JAK-STAT PATHWAY ; VIRUS-REPLICATION ; INFECTION ; LAMBDA ; HEPATOCYTES ; CELLS ; HCV ; IDENTIFICATION ; EXPRESSION
WOS研究方向Biotechnology & Applied Microbiology ; Virology
WOS类目Biotechnology & Applied Microbiology ; Virology
语种英语
出版者MICROBIOLOGY SOC
WOS记录号WOS:000385291700018
URI标识http://www.irgrid.ac.cn/handle/1471x/2374813
专题中国科学院大学
通讯作者Niu, Junqi; Zhong, Jin; Sun, Bing
作者单位1.Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Mol Virol & Immunol,Inst Pasteur Shanghai, Shanghai 200031, Peoples R China
2.Shanghai Tech Univ, Sch Life Sci & Technol, Shanghai 200031, Peoples R China
3.Jilin Univ, Hosp 1, Hepatol Sect, Changchun 130021, Jilin, Peoples R China
4.Inst Biochem & Cell Biol, Lab Mol Cell Biol, Shanghai, Peoples R China
5.Univ Texas Southwestern Med Ctr Dallas, Dept Obstet & Gynecol, Cecil H & Ida Green Ctr Reprod Biol Sci, Dallas, TX 75390 USA
推荐引用方式
GB/T 7714
Fan, Weiguo,Xie, Shiqi,Zhao, Xinhao,et al. Ifn-lambda 4 desensitizes the response to ifn-alpha treatment in chronic hepatitis c through long-term induction of usp18[J]. Journal of general virology,2016,97:2210-2220.
APA Fan, Weiguo.,Xie, Shiqi.,Zhao, Xinhao.,Li, Nan.,Chang, Chong.,...&Sun, Bing.(2016).Ifn-lambda 4 desensitizes the response to ifn-alpha treatment in chronic hepatitis c through long-term induction of usp18.Journal of general virology,97,2210-2220.
MLA Fan, Weiguo,et al."Ifn-lambda 4 desensitizes the response to ifn-alpha treatment in chronic hepatitis c through long-term induction of usp18".Journal of general virology 97(2016):2210-2220.

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来源:中国科学院大学

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