Walker Christopher M, Grakoui Arash
Department of Pediatrics, Nationwide Children's Hospital and The Ohio State University School of Medicine, 700 Children's Drive, Columbus, OH 43004, United States.
Yerkes National Primate Research Center, Emory Vaccine Center, Emory University, Atlanta, GA 30329, United States; Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA 30322, United States.
Curr Opin Immunol. 2015 Aug;35:137-43. doi: 10.1016/j.coi.2015.06.010. Epub 2015 Aug 1.
Chronic hepatitis C virus infection is now curable by antiviral therapy but the global burden of liver disease is unlikely to diminish without a vaccine to prevent transmission. The objective of HCV vaccination is not to induce sterilizing immunity, but instead to prevent persistent infection. One vaccine that incorporates only non-structural HCV proteins is now in phase I/II efficacy trials to test the novel concept that T cell priming alone is sufficient for protection. Evidence also suggests that antibodies contribute to infection resolution. Vaccines comprised of recombinant envelope glycoproteins targeted by neutralizing antibodies have been assessed in humans for immunogenicity. Here, we discuss current concepts in protective immunity and divergent approaches to vaccination against a highly mutable RNA virus.
慢性丙型肝炎病毒感染现在可以通过抗病毒疗法治愈,但如果没有预防传播的疫苗,全球肝脏疾病负担不太可能减轻。丙型肝炎病毒疫苗接种的目标不是诱导无菌免疫,而是预防持续性感染。一种仅包含丙型肝炎病毒非结构蛋白的疫苗目前正处于I/II期疗效试验阶段,以测试仅T细胞启动就足以提供保护的新概念。证据还表明,抗体有助于感染的消除。由中和抗体靶向的重组包膜糖蛋白组成的疫苗已在人体中评估其免疫原性。在此,我们讨论保护性免疫的当前概念以及针对高度可变RNA病毒的不同疫苗接种方法。