Immunization with a peptide vaccine increased virus-specific CD8+ T cells, reduced viral RNA, and lessened liver injury, demonstrating that T cells protect against HAV-mediated liver injury.
Do T cells protect against HAV-mediated liver injury in a mouse model?
In a mouse model, virus-specific T cells protect against Hepatitis A virus infection and limit liver injury, challenging the notion that T cells exacerbate liver disease in this context.
BACKGROUND & AIMS: Hepatitis A virus (HAV) is a common cause of enterically transmitted viral hepatitis. In non-immune individuals, infection results in typically transient but occasionally fulminant and fatal inflammatory liver injury. Virus-specific T cell frequencies peak when liver damage is at its zenith, leading to the prevalent notion that T cells exacerbate liver disease, as suspected for other hepatotropic virus infections. However, the overall contribution of T cells to the control of HAV and the pathogenesis of hepatitis A is unclear and has been impeded by a historic lack of small animal models. METHODS: mice are highly permissive for HAV and develop pathogenesis that recapitulates many features of hepatitis A. Using this model, we identified HAV-specific CD8+ and CD4+ T cells by epitope mapping, and then used tetramers and functional assays to quantify T cells in the liver at multiple times after infection. We assessed the relationships between HAV-specific T cell frequency, viral RNA amounts, and liver pathogenesis. RESULTS: mice during the first 1-2 weeks of infection and persisted over time. HAV replication was enhanced and liver disease exacerbated when mice were depleted of T cells. Conversely, immunization with a peptide vaccine increased virus-specific CD8+ T cell frequencies in the liver, reduced viral RNA abundance, and lessened liver injury. CONCLUSION: These data show that T cells protect against HAV-mediated liver injury and can be targeted to improve liver health. LAY SUMMARY: Hepatitis A virus is a leading cause of acute viral hepatitis worldwide. T cells were thought to contribute to liver injury during acute infection. We now show that virus-specific T cells protect against infection and limit liver injury.
Misumi et al. (Wed,) conducted a other in Hepatitis A virus infection. T cell depletion and peptide vaccine immunization was evaluated on HAV replication and liver pathogenesis. Immunization with a peptide vaccine increased virus-specific CD8+ T cells, reduced viral RNA, and lessened liver injury, demonstrating that T cells protect against HAV-mediated liver injury.
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