首页> 外文期刊>Liver international : >Identification of host and viral factors involved in a dissimilar resolution of a hepatitis C virus infection
【24h】

Identification of host and viral factors involved in a dissimilar resolution of a hepatitis C virus infection

机译:鉴定与丙型肝炎病毒感染不同解决方案有关的宿主和病毒因素

获取原文
获取原文并翻译 | 示例
           

摘要

Background & Aims: Hepatitis C virus (HCV) transmission from a chronic patient to a susceptible individual is a good opportunity to study viral and host factors that may influence the natural course of hepatitis C infection towards either spontaneous recovery or chronicity. To compare a documented case of a bottleneck event in the sexual transmission of HCV from a chronically infected patient to a recipient host that cleared infection. Methods: Host genetic components such as Class I and II HLA and IL28B polymorphism (rs12979860 SNPs) were identified by direct sequencing and LightMix analysis, respectively. Deep nucleotide sequence analysis of quasispecies complexity was performed using massive pyrosequencing platform (454 GS-FLX), and the CD4 specific immune response was characterized by ELISPOT. Results and Conclusions: Sequencing analysis and CD4 response highlighted several NS3-helicase domains in which an interplay between amino acid variability and CD4 immune response might have contributed either to chronicity in the donor patient or to viral clearance in the receptor (newly infected) patient.
机译:背景与目的:丙型肝炎病毒(HCV)从慢性患者到易感人群的传播是研究病毒和宿主因素的好机会,这些因素可能会影响丙型肝炎感染自然过程的自然恢复或慢性化。为了比较HCV从慢性感染患者到清除感染的宿主的性传播过程中出现瓶颈事件的记录案例。方法:分别通过直接测序和LightMix分析鉴定宿主遗传成分,如I类和II类HLA和IL28B多态性(rs12979860 SNP)。使用大规模焦磷酸测序平台(454 GS-FLX)对准物种复杂性进行了深核苷酸序列分析,并用ELISPOT表征了CD4特异性免疫反应。结果和结论:测序分析和CD4应答突出显示了几个NS3-解旋酶结构域,其中氨基酸变异性和CD4免疫应答之间的相互作用可能导致了供体患者的慢性或受体(新感染)患者的病毒清除。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号