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慢性丙型肝炎病毒感染期间内源性肝内干扰素刺激基因的上调

Upregulation of endogenous intrahepatic interferon stimulated genes during chronic hepatitis C virus infection.

作者信息

MacQuillan Gerry C, Mamotte Cyril, Reed William D, Jeffrey Gary P, Allan Jane E

机构信息

Department of Medicine, The University of Western Australia, Western Australia.

出版信息

J Med Virol. 2003 Jun;70(2):219-27. doi: 10.1002/jmv.10381.

Abstract

The success of interferon-alpha and ribavirin combination therapy for the treatment of chronic hepatitis C viral infection differs between patients. In an attempt to identify predictors of host response to therapy, the levels of mRNA for interferon (IFN) stimulated genes: MxA, PKR, 2'5' OAS, ISG15, and interleukin 8 (IL-8), were examined in liver by real-time RT-PCR prior to commencement of therapy. The levels of intrahepatic classical IFN stimulated genes, but not IL-8, in chronic HCV disease (n = 44) were found to be significantly upregulated (P < 0.001) compared to the control cohort (n = 12). The genotype of the infecting HCV strain did not influence IFN stimulated gene expression. These results suggest that the endogenous type 1 IFN antiviral effector pathway is broadly activated during chronic HCV disease, although the levels of mRNA for any of the IFN-stimulated genes tested did not predict the outcome of combination therapy.

摘要

α干扰素与利巴韦林联合治疗慢性丙型肝炎病毒感染的疗效在患者之间存在差异。为了确定宿主对治疗反应的预测指标,在治疗开始前,通过实时逆转录聚合酶链反应(RT-PCR)检测肝脏中干扰素(IFN)刺激基因:Mx A、PKR、2'5'寡腺苷酸合成酶(OAS)、ISG15和白细胞介素8(IL-8)的mRNA水平。与对照组(n = 12)相比,慢性丙型肝炎患者(n = 44)肝脏中经典的IFN刺激基因水平显著上调(P < 0.001),但IL-8水平未上调。感染的HCV毒株基因型不影响IFN刺激基因的表达。这些结果表明,在慢性丙型肝炎疾病期间,内源性1型IFN抗病毒效应途径被广泛激活,尽管所检测的任何IFN刺激基因的mRNA水平均不能预测联合治疗的结果。

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