Mechanisms of Hepatocellular Injury in Hepatitis A

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.

Automated summary

Hepatitis A virus (HAV) infection is a common cause of acute viral hepatitis, and while virus-specific cytotoxic T cells were previously believed to be responsible for liver injury, recent evidence suggests that natural killer (NK) cells, NKT cells, and even non-HAV-specific CD8(+) T cells may also contribute to liver damage. Intrinsic death of virus-infected hepatocytes and genetic variations in host factors have also been linked to hepatitis A severity. Understanding these mechanisms could improve diagnosis and treatment of diseases associated with HAV infection.