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Prophylaxis against Recurrence in Liver Transplantation Patients with Hepatitis B Virus: What is New?
Özgür Harmancı1, Haldun Selçuk1, Mehmet Haberal2
1Department of Gastroenterology, Başkent University Medical School, Ankara, Turkey.
Insights
Hepatitis B virus (HBV) infection recurrence after liver transplantation (LT) is linked to HBV-host genome interactions. Nucleoside/nucleotide analogs offer new treatment options to overcome this challenge.
Area of Science:
- Hepatology
- Virology
- Genetics
Background:
- Hepatitis B virus (HBV) infection is a global health issue affecting nearly 2 billion people.
- HBV is a primary cause of liver cirrhosis, hepatocellular carcinoma (HCC), and liver transplantation (LT).
- Recurrence of HBV infection post-LT is a significant clinical problem driven by HBV-host genome interactions.
Purpose of the Study:
- To review the challenges and advancements in managing Hepatitis B virus recurrence after liver transplantation.
- To highlight the role of nucleoside and nucleotide analogs in preventing HBV recurrence.
Main Methods:
- Review of current literature on HBV recurrence post-LT.
- Analysis of treatment strategies, including hepatitis B immunoglobulin and antiviral nucleoside/nucleotide analogs.
- Discussion of HBV-host genome interactions influencing recurrence.
Main Results:
- Hepatitis B immunoglobulin has been a standard treatment, but resistance can occur.
- Nucleoside and nucleotide analogs, particularly those with a high genetic barrier to resistance, show promise.
- Combination therapies may offer enhanced efficacy in preventing HBV recurrence.
Conclusions:
- HBV recurrence post-LT remains a critical concern.
- Advanced nucleoside and nucleotide analogs represent powerful therapeutic options for managing HBV recurrence.
- Further research into HBV-host interactions can refine treatment strategies.
Abstract:
Hepatitis B virus (HBV) causes an endemic infection that affects nearly 2 billion patients worldwide. It is one of the leading causes of liver cirrhosis, hepatocellular carcinoma (HCC), and liver transplantation (LT). Recurrence of HBV infection after LT is due to specific HBV-host genome interactions. Although hepatitis B immunoglobulin treatment constituted the backbone of HBV recurrence, use of the nucleoside and nucleotide analogs (especially the ones with a higher genetic barrier to resistance), either alone or in combination, offer us new and powerful options in overcoming this serious issue.
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