Genomic analysis of the host response to hepatitis C virus infection

被引:527
作者
Su, AI
Pezacki, JP
Wodicka, L
Brideau, AD
Supekova, L
Thimme, R
Wieland, S
Bukh, J
Purcell, RH
Schultz, PG
Chisari, FV [1 ]
机构
[1] The Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] The Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[3] Novartis Res Fdn, Genomics Inst, San Diego, CA 92121 USA
[4] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
[5] NIH, Hepatitis Viruses Sect, Infect Dis Lab, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.202608199
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have examined the progression of hepatitis C virus (HCV) infections by gene expression analysis of liver biopsies in acutely infected chimpanzees that developed persistent infection, transient viral clearance, or sustained clearance. Both common responses and outcome-specific changes in expression were observed. All chimpanzees showed gene expression patterns consistent with an IFN-alpha response that correlated with the magnitude and duration of infection. Transient and sustained viral clearance were uniquely associated with induction of IFN-gamma-induced genes and other genes involved in antigen processing and presentation and the adaptive immune response. During the early stages of infection, host genes involved in lipid metabolism were also differentially regulated. We also show that drugs that affect these biosynthetic pathways can regulate HCV replication in HCV replicon systems. Our results reveal genome-wide transcriptional changes that reflect the establishment, spread, and control of infection, and they reveal potentially unique antiviral programs associated with clearance of HCV infection.
引用
收藏
页码:15669 / 15674
页数:6
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