首页> 中文期刊> 《中华医学杂志(英文版)》 >Direct-acting Antiviral Agents Resistance-associated Polymorphisms in Chinese Treatment-na(i)ve Patients Infected with Genotype 1b Hepatitis C Virus

Direct-acting Antiviral Agents Resistance-associated Polymorphisms in Chinese Treatment-na(i)ve Patients Infected with Genotype 1b Hepatitis C Virus

         

摘要

Background:It has been reported that several baseline polymorphisms of direct-acting antivirals (DAAs) agents resistance-associated variants (RAVs) would affect the treatment outcomes of patients chronically infected with hepatitis C virus (CHC).The aim of this study is to investigate the prevalence of DAAs RAVs in treatment-na(i)ve GT1b CHC patients.Methods:Direct sequencing and ultra-deep sequencing of the HCV NS3,NS5A,and NS5B gene were performed in baseline serum samples of treatment-ha(i)ve patients infected with genotype lb hepatitis C virus (HCVs).Results:One hundred and sixty CHC patients were studied.Complete sequence information was obtained for 145 patients (NS3),148 patients (NS5A),and 137 patients (NS5B).Treatment-failure associated variants of DAAs were detected:56.6% (82/145) of the patients presented S122G for simeprevir (NS3 protease inhibitor);10.1% (14/148) of the patients presented Y93H for daclatasvir and ledipasvir (NS5A protein inhibitors);94.2% (129/137) of the patients presented C316N for sofosbuvir (NS5B polymerase inhibitor).Nearly,all of the DAAs RAVs detected by ultra-deep sequencing could be detected by direct sequencing.Conclusions:The majority of genotype lb CHC patients in China present a virus population carrying HCV DAAs RAVs.Pretreatment sequencing of HCV genome might need to be performed when patients infected with GTlb HCV receiving DAAs-containing regimens in China.Population sequencing would be quite quantified for the work.

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  • 来源
    《中华医学杂志(英文版)》 |2015年第19期|2625-2631|共7页
  • 作者单位

    Peking University People's Hospital,Peking University Hepatology Institute,Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease,Beijing 100044,China;

    Peking University People's Hospital,Peking University Hepatology Institute,Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease,Beijing 100044,China;

    Peking University People's Hospital,Peking University Hepatology Institute,Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease,Beijing 100044,China;

    Peking University People's Hospital,Peking University Hepatology Institute,Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease,Beijing 100044,China;

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  • 正文语种 eng
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