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[HCV reinfection after liver transplantation for HCV cirrhosis]
G Pasquale1, P Iannicelli, S Martini
1Dipartimento di Medicina Pubblica, Clinica e Preventiva, Sezione Malattie Infettive, Seconda Universita degli Studi di Napoli, Italy.
Insights
Hepatitis C virus (HCV) recurrence after liver transplantation is common and reduces survival. Current treatments like interferon and ribavirin have limitations, with many questions remaining about optimal therapy for recurrent HCV infection.
Area of Science:
- Hepatology
- Virology
- Transplantation Immunology
Context:
- Hepatitis C virus (HCV) infection is the leading cause of liver transplantation.
- Recurrence of HCV post-transplantation significantly impacts patient and graft survival.
- Risk factors for recurrent HCV disease severity are linked to viral, host, and donor characteristics.
Purpose:
- To review the challenges and therapeutic strategies for managing recurrent hepatitis C virus infection after orthotopic liver transplantation (OLT).
- To highlight the high incidence of HCV recurrence and its detrimental effects on long-term outcomes.
- To discuss current treatment limitations and identify areas needing further research.
Summary:
- Recurrent HCV infection occurs in all pre-transplant positive patients and affects 75-80% post-OLT, leading to graft cirrhosis in one-third within 5-7 years.
- Cholestatic hepatitis C can cause rapid graft failure, significantly reducing survival rates compared to other OLT indications.
- Standard treatments involve interferons and ribavirin, but Peg-interferons are limited by side effects, and optimal treatment timing, targets, and duration remain unclear.
Impact:
- Understanding recurrence patterns and risk factors is crucial for improving post-transplant management.
- Identifying effective and safe therapeutic strategies is essential to enhance long-term graft and patient survival after OLT for HCV.
- Further research is needed to clarify optimal treatment protocols for recurrent HCV infection in the allograft.
Abstract:
Cirrhosis due to hepatitis C virus (HCV) infection is now the most frequent indication for orthotopic liver transplantation (OLT). Recurrence of hepatitis C infection is the major cause of late mortality in patients undergoing OLT for hepatitis C cirrhosis. Recurrent HCV infection develops in 100% of patients HCV + in pre-transplantation time. Histological recurrence occurs in 75-80% of patients after OLT:1/3 of them progress to allograft cirrhosis within 5-7 years. Cholestatic hepatitis C develops in a sub-group of patients who progresses rapidly to graft failure. As a result of this accelerated course of HCV infection, long-term graft and patient survival are significantly reduced in patients undergoing OLT for HCV-related cirrhosis compared with other groups. Moreover, several recurrence's risk factors have been described as predictors of disease severity including those related to the virus, the host, the donor. There are numerous therapeutic strategies to prevent and to treat HCV disease recurrence after OLT. The most common strategy to treat HCV infection post-OLT is based on interferons and ribavirin. Even if clinical trials have shown that the combination of ribavirin with Peg-interferons is more effective than its association with standard interferons, the use of Peg-interferons in transplanted patients is limited by the side-effects of the drug. About treatment of hepatitis C virus infection in the allograft dark and not still cleared points are a lot: the timing and the target of therapy, the dose and duration of pharmacological treatment.
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