Su Andrew I, Pezacki John P, Wodicka Lisa, Brideau Amy D, Supekova Lubica, Thimme Robert, Wieland Stefan, Bukh Jens, Purcell Robert H, Schultz Peter G, Chisari Francis V
Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15669-74. doi: 10.1073/pnas.202608199. Epub 2002 Nov 19.
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.
我们通过对急性感染黑猩猩肝脏活检样本进行基因表达分析,研究了丙型肝炎病毒(HCV)感染的进展情况,这些黑猩猩分别出现了持续感染、短暂病毒清除或持续病毒清除。我们观察到了共同的反应以及表达上的结果特异性变化。所有黑猩猩都表现出与干扰素α反应一致的基因表达模式,该反应与感染的程度和持续时间相关。短暂和持续的病毒清除与干扰素γ诱导基因以及其他参与抗原加工呈递和适应性免疫反应的基因的诱导存在独特关联。在感染早期,参与脂质代谢的宿主基因也受到了差异调节。我们还表明,影响这些生物合成途径的药物可以在HCV复制子系统中调节HCV复制。我们的结果揭示了全基因组转录变化,这些变化反映了感染的建立、传播和控制,并且揭示了与HCV感染清除相关的潜在独特抗病毒程序。