First Department of Medicine, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan.
Intervirology. 2010;53(1):66-9. doi: 10.1159/000252787. Epub 2010 Jan 5.
The aim of this study was to search hepatitis C virus (HCV) genetic elements determining the early response to peginterferon/ribavirin therapy using HCV genome-wide analysis. From a total of 88 chronic hepatitis C patients with HCV-1b treated with peginterferon/ribavirin, the whole HCV amino acid sequence was determined and analyzed according to the viral response during the treatment. Mutations in NS5A-ISDR (interferon sensitivity-determining region) are associated with rapid viral response at week 4, and the core arginine70glutamine (R70Q) mutation is associated with no early viral response at week 12, revealing that core 70 and NS5A are the most important factors determining the virological kinetics during peginterferon and ribavirin therapy.
本研究旨在通过 HCV 全基因组分析,寻找决定聚乙二醇干扰素/利巴韦林治疗早期应答的丙型肝炎病毒(HCV)遗传因素。对 88 例接受聚乙二醇干扰素/利巴韦林治疗的 HCV-1b 慢性丙型肝炎患者,根据治疗过程中的病毒应答情况,对整个 HCV 氨基酸序列进行了测定和分析。NS5A-ISDR(干扰素敏感性决定区)中的突变与第 4 周的快速病毒应答相关,核心区精氨酸 70 位谷氨酰胺(R70Q)突变与第 12 周无早期病毒应答相关,这表明核心区 70 位和 NS5A 是决定聚乙二醇干扰素和利巴韦林治疗期间病毒动力学的最重要因素。