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Published on: September 25, 2019
Virological response for recurrent hepatitis C improves long-term survival in liver transplant recipients
Tomohiro Tanaka1, Nazia Selzner, George Therapondos
1Multi-Organ Transplant Program, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Insights
Achieving a sustained virological response (SVR) after hepatitis C virus (HCV) treatment significantly improves long-term survival for liver transplant recipients. Early virological response is critical for better patient outcomes post-transplant.
Area of Science:
- Hepatology
- Transplant Surgery
- Virology
Background:
- Recurrent hepatitis C virus (HCV) infection is a primary cause of mortality following liver transplantation (LT) for HCV-related end-stage liver disease.
- Effective management of post-transplant HCV recurrence is crucial for improving LT recipient survival.
Purpose of the Study:
- To evaluate the long-term impact of antiviral treatment response on the survival of liver transplant recipients with recurrent hepatitis C.
- To determine if sustained virological response (SVR) or relapse influences patient survival rates after LT.
Main Methods:
- A retrospective study of 245 LT recipients treated with interferon-based antiviral therapy for recurrent HCV from August 1987 to October 2011.
- Kaplan-Meier survival analysis was used to compare outcomes between patients achieving SVR, relapsers, and non-responders (NR).
- Patient survival was assessed based on virological response status, independent of other characteristics.
Main Results:
- Sustained virological response (SVR) was achieved by 51.4% of patients.
- Patients with SVR demonstrated significantly better 5-year survival (95.2%) compared to the non-response (NR) group (49.9%) (P < 0.001).
- Relapsers showed significantly longer survival than the NR group (P = 0.005), and a trend towards better survival than NR group (P = 0.14).
Conclusions:
- Virological response to antiviral therapy, particularly SVR, is a significant predictor of improved long-term patient survival after LT for hepatitis C.
- Achieving SVR markedly improves patient outcomes, highlighting the importance of successful HCV eradication post-transplantation.
- Antiviral treatment response is a key factor in managing recurrent HCV and enhancing survival in LT recipients.
Abstract:
Recurrent hepatitis C virus (HCV) infection occurs universally and is regarded as a major cause of mortality after liver transplantation (LT) for HCV-related end-stage liver disease. We conducted this large, single-center, retrospective study to ascertain the long-term impact of virological response to treatment of recurrent hepatitis C on survival of LT recipients. From August 1987 to October 2011, 285 patients have received interferon-based antiviral therapy for recurrent hepatitis C. Of these 285, 245 patients were enrolled in this study. One hundred and twenty-six patients (51.4%) achieved sustained virological response (SVR). Relapsers (undetectable HCV-RNA at end of treatment, becoming positive afterward) comprised 9.0% (22/245), and nonresponse (NR; never achieving undetectable HCV-RNA) 39.6% (97/245). The median follow-up after completion of antiviral treatment was 2081 days. Using Kaplan-Meier method, patients who achieved SVR were shown to have significantly better 5-year patient survival (95.2%) than the NR group (49.9%) (P < 0.001), and a trend toward better 5-year survival than relapsers (87.5%) (P = 0.14); relapsers had a significantly longer survival than NR group (P = 0.005). When compared with NR, SVR and relapse appeared to be significant predictors of better survival, independent of underlying characteristics. In conclusion, virological response, especially SVR, translates into markedly improved long-term patient outcomes in patients transplanted for hepatitis C.
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