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Liver transplantation for hepatitis B and C virus-related cirrhosis: mid-term results
T M Manzia1, D Di Paolo, D Sforza
1Transplant Unit, Department of Surgery, University of Rome Tor Vergata, Rome, Italy. tomanzia@libero.it
Insights
Hepatitis C virus (HCV) and Hepatitis B virus (HBV) coinfection in liver transplant recipients shows promising midterm outcomes. Patients with HBV-HCV cirrhosis had slower fibrosis progression compared to HCV-only cases.
Area of Science:
- Hepatology
- Transplantation Immunology
- Virology
Background:
- Hepatitis C virus (HCV) recurrence post-liver transplant is common, leading to cirrhosis in 30% of cases.
- Understanding outcomes for liver transplant recipients with concomitant Hepatitis B virus (HBV) infection is crucial.
Purpose of the Study:
- To retrospectively analyze midterm outcomes of liver transplant recipients with HBV-HCV coinfection.
- To compare fibrosis progression rates between HBV-HCV coinfected and HCV-monoinfected patients.
Main Methods:
- Retrospective analysis of 350 liver transplant recipients (April 1992-December 2008).
- Focus on 20 patients transplanted for HBV-HCV cirrhosis.
- Kaplan-Meier survival analysis and Ishak scoring for chronic hepatitis.
- Yearly protocol liver biopsies for fibrosis assessment.
Main Results:
- At a median follow-up of 68.4 months, 1- and 5-year patient/graft survival rates were 80% and 70%.
- The 5-year fibrosis progression rate was 0.17 +/- 0.08 units.
- One patient developed cirrhosis due to lamivudine-resistant HBV recurrence.
- HBV-HCV coinfected patients exhibited a lower fibrosis progression rate than HCV-monoinfected patients.
Conclusions:
- Liver transplantation for HBV-HCV coinfection demonstrates acceptable midterm survival rates.
- Coinfection with HBV may be associated with a slower rate of fibrosis progression post-transplant compared to HCV monoinfection.
- Monitoring for viral recurrence, especially lamivudine-resistant HBV, is essential.
Abstract:
Hepatitis C virus (HCV) recurrence after orthotopic liver transplantation (OLT) is almost universal; cirrhosis develops in up to 30% of cases. Currently there is interest in the midterm outcomes of HCV patients with concomitant hepatitis B virus (HBV) infection among OLT recipients. We therefore retrospectively analyzed our database of patients who underwent OLT for HCV-HBV-related cirrhosis. Between April 1992 and December 2008, 350 patients underwent OLT, including 20 (5.7%) transplanted for HBV-HCV cirrhosis. We assessed patient and graft survivals at 1 and 5 years, as well as the progression of fibrosis. Protocol liver biopsies were available yearly after OLT. The survival curves were analyzed by the Kaplan-Meier approach and chronic hepatitis evaluated according to the Ishak scoring system. At a median follow-up of 68.4 +/- 53 months, the 1- and 5-year patient and graft survival rates were 80% and 70%, respectively. The 5-year fibrosis progression rate was 0.17 +/- 0.08 units of fibrosis. The only patient who developed histologic cirrhosis within 10 years of follow-up showed a lamivudine-resistant HBV recurrence. Patients transplanted for HBV-HCV coinfection showed a lower fibrosis progression rate compared with HCV monoinfected subjects.
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