Colasanti Ombretta, Yu Hosun, Lohmann Volker, Shin Eui-Cheol
Heidelberg University, Medical Faculty Heidelberg, Department of Infectious Diseases, Molecular Virology, Section Virus-Host-Interactions, Center for Integrative Infectious Disease Research, Heidelberg, Germany.
Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Exp Mol Med. 2025 Apr;57(4):714-723. doi: 10.1038/s12276-025-01431-2. Epub 2025 Apr 2.
Despite the development of effective vaccines against hepatitis A virus (HAV) infection, outbreaks of acute hepatitis A still occur globally, such that HAV remains a major cause of acute viral hepatitis. Most patients with acute hepatitis A recover spontaneously; however, some adult cases result in acute liver failure due to immune-mediated liver damage. Previous studies suggested that HAV evades the innate immune response through strong counteractive mechanisms, and that HAV-specific CD8 T cells contribute to liver damage in patients with acute hepatitis A. However, recent research findings have led to revisions of old hypotheses. Here we will describe the most current knowledge regarding the innate immune response to HAV and the HAV-mediated counteractions against innate immune responses. Additionally, we will discuss the roles of various types of T cells in viral clearance and liver injury in patients with acute hepatitis A.
尽管已经开发出针对甲型肝炎病毒(HAV)感染的有效疫苗,但全球范围内仍会发生甲型肝炎急性暴发,因此HAV仍然是急性病毒性肝炎的主要病因。大多数甲型肝炎急性患者会自发康复;然而,一些成年病例会因免疫介导的肝损伤而导致急性肝衰竭。先前的研究表明,HAV通过强大的对抗机制逃避先天免疫反应,并且HAV特异性CD8 T细胞会导致甲型肝炎急性患者的肝损伤。然而,最近的研究结果导致了对旧假说的修正。在此,我们将描述关于对HAV的先天免疫反应以及HAV介导的针对先天免疫反应的对抗作用的最新知识。此外,我们还将讨论各类T细胞在甲型肝炎急性患者的病毒清除和肝损伤中的作用。