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Updated: Jun 30, 2025

Induction of Drug-Induced, Autoimmune Hepatitis in BALB/c Mice for the Study of Its Pathogenic Mechanisms
Published on: May 29, 2020
Management of autoimmune hepatitis induced by hepatitis delta virus
Eleni Gigi1, Vasileios Lagopoulos2, Aris Liakos3
1Hepatology Unit, The Second Internal Medicine Department, Aristotle University Medical School, Hippokrateio General Hospital, Thessaloniki 54642, Greece. elengigi@auth.gr.
Insights
Hepatitis B (HBV) and hepatitis D (HDV) co-infection can cause severe liver disease. The link between viral hepatitis and autoimmune hepatitis (AIH) requires further study to guide treatment for co-infected patients.
Area of Science:
- Hepatology
- Immunology
- Virology
Background:
- Hepatitis B virus (HBV) and hepatitis D virus (HDV) co-infection affects millions globally, leading to severe liver conditions like cirrhosis and hepatocellular carcinoma.
- A known correlation exists between viral hepatitis and autoimmune diseases, with autoantibodies detected in HBV/HDV co-infected patients.
- Clinically significant autoimmune hepatitis (AIH) is rarely reported in HDV-infected individuals, particularly those treated with pegylated interferon, raising diagnostic and etiological questions.
Abstract:
Approximately 12-72 million people worldwide are co-infected with hepatitis B virus (HBV) and hepatitis delta virus (HDV). This concurrent infection can lead to several severe outcomes with hepatic disease, such as cirrhosis, fulminant hepatitis, and hepatocellular carcinoma, being the most common. Over the past few decades, a correlation between viral hepatitis and autoimmune diseases has been reported. Furthermore, autoantibodies have been detected in the serum of patients co-infected with HBV/HDV, and autoimmune features have been reported. However, to date, very few cases of clinically significant autoimmune hepatitis (AIH) have been reported in patients with HDV infection, mainly in those who have received treatment with pegylated interferon. Interestingly, there are some patients with HBV infection and AIH in whom HDV infection is unearthed after receiving treatment with immunosuppressants. Consequently, several questions remain unanswered with the challenge to distinguish whether it is autoimmune or "autoimmune-like" hepatitis being the most crucial. Second, it remains uncertain whether autoimmunity is induced by HBV or delta virus. Finally, we investigated whether the cause of AIH lies in the previous treatment of HDV with pegylated interferon. These pressing issues should be elucidated to clarify whether new antiviral treatments for HDV, such as Bulevirtide or immu-nosuppressive drugs, are more appropriate for the management of patients with HDV and AIH.
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