Inserm, U748, Strasbourg, France.
Université de Strasbourg, Strasbourg, France.
Gastroenterology. 2012 Jul;143(1):223-233.e9. doi: 10.1053/j.gastro.2012.04.006. Epub 2012 Apr 10.
BACKGROUND & AIMS: The development of vaccines and other strategies to prevent hepatitis C virus (HCV) infection is limited by rapid viral evasion. HCV entry is the first step of infection; this process involves several viral and host factors and is targeted by host-neutralizing responses. Although the roles of host factors in HCV entry have been well characterized, their involvement in evasion of immune responses is poorly understood. We used acute infection of liver graft as a model to investigate the molecular mechanisms of viral evasion.
We studied factors that contribute to evasion of host immune responses using patient-derived antibodies, HCV pseudoparticles, and cell culture-derived HCV that express viral envelopes from patients who have undergone liver transplantation. These viruses were used to infect hepatoma cell lines that express different levels of HCV entry factors.
By using reverse genetic analyses, we identified altered use of host-cell entry factors as a mechanism by which HCV evades host immune responses. Mutations that alter use of the CD81 receptor also allowed the virus to escape neutralizing antibodies. Kinetic studies showed that these mutations affect virus-antibody interactions during postbinding steps of the HCV entry process. Functional studies with a large panel of patient-derived antibodies showed that this mechanism mediates viral escape, leading to persistent infection in general.
We identified a mechanism by which HCV evades host immune responses, in which use of cell entry factors evolves with escape from neutralizing antibodies. These findings advance our understanding of the pathogenesis of HCV infection and might be used to develop antiviral strategies and vaccines.
疫苗和其他预防丙型肝炎病毒(HCV)感染的策略的发展受到病毒快速逃逸的限制。HCV 进入是感染的第一步;这一过程涉及几种病毒和宿主因素,并受到宿主中和反应的靶向作用。尽管宿主因素在 HCV 进入中的作用已得到很好的描述,但它们在逃避免疫反应中的作用知之甚少。我们使用肝移植后的急性感染作为模型来研究病毒逃逸的分子机制。
我们使用来自接受过肝移植的患者的患者源性抗体、HCV 假病毒和细胞培养衍生的 HCV,研究了导致宿主免疫反应逃避的因素。这些病毒用于感染表达不同水平 HCV 进入因子的肝癌细胞系。
通过使用反向遗传学分析,我们确定了改变宿主细胞进入因子的使用是 HCV 逃避宿主免疫反应的一种机制。改变 CD81 受体使用的突变也使病毒能够逃避中和抗体。动力学研究表明,这些突变会影响 HCV 进入过程中结合后步骤中的病毒-抗体相互作用。使用大量患者源性抗体的功能研究表明,这种机制介导了病毒逃逸,导致普遍的持续性感染。
我们确定了 HCV 逃避宿主免疫反应的一种机制,其中细胞进入因子的使用随着中和抗体的逃逸而演变。这些发现加深了我们对 HCV 感染发病机制的理解,并可能用于开发抗病毒策略和疫苗。