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Published on: February 19, 2019
Liver Transplantation in Hepatitis B/Hepatitis D (Delta) Virus Coinfected Recipients
Silvia Martini1, Francesco Tandoi2, Renato Romagnoli2
1Gastrohepatology Unit, Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino, University of Turin, Turin, Italy.
Insights
Hepatitis D virus (HDV) causes severe hepatitis, with liver transplantation being the only cure. This review details liver transplant advancements for HDV and discusses cost-saving prophylaxis strategies.
Area of Science:
- Hepatology
- Virology
- Transplant Surgery
Background:
- Hepatitis D virus (HDV) causes the most severe form of viral hepatitis, rapidly progressing to cirrhosis.
- Liver transplantation is the sole therapeutic option for end-stage HDV disease, but access is limited in endemic regions.
- Hepatitis B virus (HBV) vaccination has reduced HDV prevalence in high-income countries, shifting transplant demand to older patients with prior HDV infection.
Purpose of the Study:
- To review the historical evolution and future prospects of liver transplantation for Hepatitis D.
- To analyze the progress in preventing HDV reinfection post-transplant.
- To explore cost-effective strategies for HDV prophylaxis by reassessing immunoglobulin use.
Main Methods:
- Literature review of liver transplantation for HDV from 1987 to present.
- Analysis of current prophylaxis protocols for HDV reinfection.
- Evaluation of the role of hepatitis B surface antigen immunoglobulins and antivirals.
Main Results:
- Liver transplantation has evolved significantly for HDV, with ongoing improvements in outcomes.
- Current standard prophylaxis involves indefinite combination therapy with HBV antivirals and anti-HBs immunoglobulins.
- The biology of HDV suggests potential for optimizing prophylaxis, possibly reducing immunoglobulin requirements and costs.
Conclusions:
- Liver transplantation remains crucial for terminal HDV, with a history of evolving techniques and outcomes.
- Prophylaxis against HDV reinfection is successful but can be optimized for cost-effectiveness.
- Future strategies may involve tailored immunoglobulin administration based on HDV biology to reduce treatment burdens.
Abstract:
Hepatitis D is caused by the hepatitis D virus (HDV); it is the most severe form of viral hepatitis in humans, running an accelerated course to cirrhosis. There is no efficacious therapy, and liver transplantation provides the only therapeutic option for terminal HDV disease. However, HDV infection is prevalent in poor countries of the world with no access to liver transplant programs; liver grafting has been performed in high-income countries, where the prevalence of the infection has much diminished as a secondary effect of hepatitis B virus vaccination, and the demand for liver transplantation outlives in aging cirrhotics who acquired hepatitis D decades ago. This review describes the evolution of liver transplantation for HDV disease from its inception in 1987 to the present time, with an outlook to its future. It reports the progress in the prophylaxis of HDV reinfections to the success of the current standard of indefinite combination of hepatitis B virus antivirals with immunoglobulins against the hepatitis B surface antigen; however, the unique biology of the virus provides a rationale to reducing costs by limiting the administration of the immunoglobulins against the hepatitis B surface antigen.
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