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接受利巴韦林单药治疗的慢性丙型肝炎病毒感染患者中丙型肝炎病毒基因组的演变。

Evolution of hepatitis C virus genome in chronically infected patients receiving ribavirin monotherapy.

作者信息

Querenghi F, Yu Q, Billaud G, Maertens G, Trépo C, Zoulim F

机构信息

INSERM Unit 271, 151 cours Albert Thomas, 69003 Lyon, France.

出版信息

J Viral Hepat. 2001 Mar;8(2):120-31. doi: 10.1046/j.1365-2893.2001.00265.x.

Abstract

Recent results of clinical trials suggest that combination of interferon and ribavirin exhibits an enhanced antiviral effect in the treatment of chronic hepatitis C. To investigate the effect of ribavirin on hepatitis C virus (HCV) infection, we analysed the evolution of the genetic heterogeneity of HCV in relation to the anti-HCV humoral response in patients treated by ribavirin alone. The study population included 35 patients with liver biopsy proven chronic hepatitis C infected with HCV genotype 1. Among them, 26 were treated with ribavirin for at least 12 months and nine untreated patients served as a control group. Serum samples were analysed before and at 6 and 12 months of therapy. Three regions of the HCV genome, i.e. HVR1, a domain of NS5A including part of the interferon sensitivity determining region (ISDR), and a segment of NS5B, were amplified by RT-PCR using specific primers. The PCR products were then studied using single-strand conformation polymorphism (SSCP) analysis followed by either direct sequencing, or cloning and sequencing. In parallel, the humoral anti-E1 response was studied using an ELISA (Innotest HCV E1Ab, Innogenetics). The results of HCV genome analysis showed no significant effect on the amino acid sequence evolution of the HVR1, NS5A and NS5B regions of HCV. Analysis of a phylogenetic tree from the major quasispecies variants showed the absence of correlation with ribavirin response, and the absence of selection of viral strains during ribavirin treatment. A trend towards a decrease in the anti-E1 Ab response was also observed. Altogether these results suggest that ribavirin may not exhibit a direct antiviral effect, but may trigger a favourable response to interferon by modulating the immune response against HCV.

摘要

近期临床试验结果表明,干扰素与利巴韦林联合使用在治疗慢性丙型肝炎时具有增强的抗病毒效果。为了研究利巴韦林对丙型肝炎病毒(HCV)感染的影响,我们分析了单独接受利巴韦林治疗的患者中HCV基因异质性的演变与抗HCV体液反应的关系。研究人群包括35例经肝活检证实感染HCV 1型的慢性丙型肝炎患者。其中,26例接受利巴韦林治疗至少12个月,9例未治疗患者作为对照组。在治疗前以及治疗6个月和12个月时对血清样本进行分析。使用特异性引物通过逆转录聚合酶链反应(RT-PCR)扩增HCV基因组的三个区域,即高变区1(HVR1)、包含部分干扰素敏感性决定区(ISDR)的NS5A结构域以及NS5B片段。然后使用单链构象多态性(SSCP)分析研究PCR产物,随后进行直接测序或克隆及测序。同时,使用酶联免疫吸附测定法(ELISA,Innotest HCV E1Ab,Innogenetics)研究体液抗E1反应。HCV基因组分析结果显示,对HCV的HVR1、NS5A和NS5B区域的氨基酸序列演变没有显著影响。对主要准种变体的系统发育树分析表明,与利巴韦林反应无关,并且在利巴韦林治疗期间没有选择病毒株。还观察到抗E1抗体反应有下降趋势。总之,这些结果表明,利巴韦林可能不具有直接抗病毒作用,但可能通过调节针对HCV的免疫反应引发对干扰素的良好反应。

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