Journal
JOURNAL OF HEPATOLOGY
Volume 75, Issue 6, Pages 1323-1334Publisher
ELSEVIER
DOI: 10.1016/j.jhep.2021.07.019
Keywords
Hepatitis A Virus; mice; liver infection; liver pathogenesis; T cells; T cell vaccine; type-1 interferons
Categories
Funding
- NIH [R01-AI131685, R01-AI143894, R01-AI138337, R01-AI103083, R01-AI150 095]
- NCI Center Core Support Grant [P30CA016086]
- Center for AIDS Research [5P30AI050410]
- North Carolina Biotech Center Institutional Support Grant [2012-IDG-1006]
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The study shows that T cells protect against liver injury caused by HAV and can be targeted to improve liver health.
Background & Aims: Hepatitis A virus (HAV) is a common cause of enterically transmitted viral hepatitis. In non-immune in-dividuals, 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: Ifnar1(-/-)mice are highly permissive for HAV and develop pathogenesis that recapitulates many features of hepa-titis 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: A large population of virus-specific T cells accumulated within the livers of Ifnar1(-/-)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. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of Euro-pean Association for the Study of the Liver.
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