Center for Vaccines and Immunity, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.
Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH 43210, USA.
Viruses. 2021 May 8;13(5):861. doi: 10.3390/v13050861.
Hepatitis A virus (HAV) infection is a common cause of acute viral hepatitis worldwide. Despite decades of research, the pathogenic mechanisms of hepatitis A remain incompletely understood. As the replication of HAV is noncytopathic in vitro, a widely accepted concept has been that virus-specific cytotoxic T cells are responsible for liver injury. However, accumulating evidence suggests that natural killer (NK) cells, NKT cells, and even non-HAV-specific CD8 T cells contribute to liver damage during HAV infection. In addition, intrinsic death of virus-infected hepatocytes has been implicated as a cause of liver injury in a murine model of hepatitis A. Furthermore, genetic variations in host factors such as T cell immunoglobulin-1 (TIM1) and IL-18 binding protein (IL-18BP) have been linked to hepatitis A severity. This review summarizes the current knowledge of the mechanisms of hepatocellular injury in hepatitis A. Different mechanisms may be involved under different conditions and they are not necessarily mutually exclusive. A better understanding of these mechanisms would aid in diagnosis and treatment of diseases associated with HAV infection.
甲型肝炎病毒(HAV)感染是全球范围内急性病毒性肝炎的常见病因。尽管已经进行了数十年的研究,但甲型肝炎的发病机制仍不完全清楚。由于 HAV 在体外的复制是非细胞病变的,因此一个被广泛接受的概念是,病毒特异性细胞毒性 T 细胞是导致肝损伤的原因。然而,越来越多的证据表明,自然杀伤(NK)细胞、NKT 细胞,甚至非 HAV 特异性 CD8 T 细胞在 HAV 感染期间有助于肝损伤。此外,在甲型肝炎的小鼠模型中,已发现感染的肝细胞内在死亡是肝损伤的一个原因。此外,宿主因素(如 T 细胞免疫球蛋白-1(TIM1)和白细胞介素-18 结合蛋白(IL-18BP))中的遗传变异与甲型肝炎的严重程度有关。本综述总结了甲型肝炎中肝细胞损伤的机制的现有知识。不同的机制可能在不同的条件下涉及,它们不一定相互排斥。更好地了解这些机制将有助于诊断和治疗与 HAV 感染相关的疾病。