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Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
Immunology of hepatitis B and hepatitis C virus infections
Andre Boonstra1, Andrea M Woltman, Harry L A Janssen
1Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. p.a.boonstra@erasmusmc.nl
Insights
Hepatitis B (HBV) and hepatitis C (HCV) infections cause chronic liver inflammation. Early immune responses influence adaptive immunity, potentially leading to immune failure in chronic patients.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Hepatitis B virus (HBV) and hepatitis C virus (HCV) are leading causes of chronic liver inflammation globally.
- Both viruses are hepatotropic and not directly cytopathic, leading to shared aspects in liver disease progression.
- HBV and HCV infections exhibit common features in adaptive antiviral immune responses.
Purpose of the Study:
- To describe the innate immune response in the early phase of HBV and HCV infections.
- To elucidate how early immune events impact the development of adaptive immune responses.
- To evaluate mechanisms contributing to immunological failure in chronic hepatitis B and C.
Main Methods:
- Review of innate and adaptive immune responses in HBV and HCV infections.
- Analysis of factors influencing immune response development.
- Evaluation of mechanisms maintaining viral-specific immunological failure.
Main Results:
- Early innate immune responses play a crucial role in shaping adaptive immunity.
- High viral antigen load, liver immune environment, regulatory T cells, and impaired dendritic cells contribute to immune failure.
- Distinct virologic features of HBV and HCV lead to shared immunological challenges.
Conclusions:
- Understanding early immune responses is critical for managing chronic hepatitis B and C.
- Mechanisms of immune evasion by HBV and HCV contribute to persistent infection.
- Targeting these mechanisms may offer therapeutic strategies for chronic viral hepatitis.
Abstract:
Hepatitis B (HBV) and hepatitis C (HCV) viruses are the two major causes of chronic liver inflammation worldwide. Despite distinct virologic features, both viruses are preferentially hepatotropic, not directly cytopathic, and elicit liver diseases that share several aspects of their natural history. HBV and HCV infections also share some important features of the adaptive antiviral immune response. We describe the innate immune response in the early phase following infection, and how these early events may influence the development of the adaptive immune response in these two important viral infections. The mechanisms by which high levels of viral antigens, liver immunological features, the presence of regulatory T cells and impaired dendritic cell functions may maintain the HBV- and HCV-specific immunological failure, characteristic of chronic hepatitis B and C patients, are also evaluated.
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