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Ribavirin/interferon-alpha sequential treatment of recurrent hepatitis C after liver transplantation
Emiliano Giostra1, Gerd A Kullak-Ublick, Walter Keller
1Division of Gastroenterology and Hepatology, University Hospital of Geneva, rue Micheli-du-Crest 24, 1211 Geneva, Switzerland.
Insights
Hepatitis C virus (HCV) recurrence post-liver transplant (LT) is common. Ribavirin and interferon-alpha (IFN-alpha) therapy can lead to sustained virological response in some patients, improving liver inflammation.
Area of Science:
- Hepatology
- Virology
- Transplantation Medicine
Background:
- Hepatitis C virus (HCV) infection frequently recurs after liver transplantation (LT).
- Graft hepatitis sequels are a major cause of morbidity and mortality in LT recipients.
- Effective management of recurrent HCV post-LT is crucial.
Purpose of the Study:
- To evaluate the efficacy of sequential ribavirin and interferon-alpha (IFN-alpha) therapy for recurrent Hepatitis C virus (HCV) infection after liver transplantation (LT).
Main Methods:
- An uncontrolled trial involving 31 patients with histologically confirmed recurrent HCV post-LT.
- Sequential therapy: 12 weeks of ribavirin, followed by 48 weeks of ribavirin plus IFN-alpha.
- Intent-to-treat analysis to assess viral load and sustained response.
Main Results:
- Sustained virological response (undetectable HCV RNA 24 weeks post-treatment) was achieved in 29% of patients (9/31).
- Sustained responders showed significant improvement in liver inflammatory activity scores.
- Sustained response correlated with treatment duration, not HCV genotype or baseline viral load.
Conclusions:
- Ribavirin/IFN-alpha therapy may benefit patients with recurrent HCV post-LT.
- Treatment tolerance and sufficient duration are key factors for achieving sustained virological response.
- Further research into optimizing treatment duration and regimens is warranted.
Abstract:
Hepatitis C virus (HCV) infection invariably recurs after liver transplantation (LT), and sequels of chronic hepatitis of the graft are a significant cause of morbidity and mortality. In an uncontrolled trial, 31 patients with histologically confirmed hepatitis C after LT received, sequentially, ribavirin (10 mg/kg body weight q.d.) for 12 weeks, followed by ribavirin at the same dose q.d. plus interferon-alpha (IFN-alpha) [3 million units three times a week (3 MU TIW)] for another 48 weeks. Based on an intent-to-treat analysis, the percentages of patients with undetectable HCV RNA in their serum were 0%, 38.7% and 45.2% after 12, 36 and 60 weeks of therapy, respectively. A sustained virological response, as defined by undetectable serum HCV RNA 24 weeks after the end of treatment, was observed in 9/31 patients (29%). Sustained responders had a significant improvement of their liver inflammatory activity score (P=0.025), but not of their liver fibrosis score. The chances of sustained virological response correlated with the length of treatment, but not with the HCV genotype or baseline HCV RNA level. In conclusion, patients with recurrent hepatitis C after LT might benefit from ribavirin/IFN-alpha therapy, provided that the treatment is tolerated for a sufficient duration of time.
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