Center for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA.
Medical Scientist Training Program, College of Medicine and Public Health, The Ohio State University, Columbus, OH, 43210, USA.
Nat Commun. 2019 Mar 7;10(1):1113. doi: 10.1038/s41467-019-09105-0.
Efforts to develop an effective vaccine against the hepatitis C virus (HCV; human hepacivirus) have been stymied by a lack of small animal models. Here, we describe an experimental rat model of chronic HCV-related hepacivirus infection and its response to T cell immunization. Immune-competent rats challenged with a rodent hepacivirus (RHV) develop chronic viremia characterized by expansion of non-functional CD8 T cells. Single-dose vaccination with a recombinant adenovirus vector expressing hepacivirus non-structural proteins induces effective immunity in majority of rats. Resolution of infection coincides with a vigorous recall of intrahepatic cellular responses. Host selection of viral CD8 escape variants can subvert vaccine-conferred immunity. Transient depletion of CD8 cells from vaccinated rats prolongs infection, while CD4 cell depletion results in chronic viremia. These results provide direct evidence that co-operation between CD4 and CD8 T cells is important for hepacivirus immunity, and that subversion of responses can be prevented by prophylactic vaccination.
开发针对丙型肝炎病毒 (HCV; 人类嗜肝病毒) 的有效疫苗的努力因缺乏小动物模型而受阻。在这里,我们描述了一种慢性丙型肝炎相关嗜肝病毒感染的实验大鼠模型及其对 T 细胞免疫的反应。用啮齿动物嗜肝病毒 (RHV) 挑战免疫功能正常的大鼠会导致慢性病毒血症,其特征是无功能 CD8 T 细胞的扩增。单次接种表达丙型肝炎病毒非结构蛋白的重组腺病毒载体可诱导大多数大鼠产生有效免疫。感染的消除与肝内细胞反应的强烈回忆相一致。病毒 CD8 逃逸变体的宿主选择可以颠覆疫苗赋予的免疫。从接种疫苗的大鼠中短暂耗尽 CD8 细胞会延长感染,而 CD4 细胞耗尽则会导致慢性病毒血症。这些结果提供了直接证据,证明 CD4 和 CD8 T 细胞之间的合作对于嗜肝病毒免疫很重要,并且通过预防性疫苗接种可以防止反应的颠覆。