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Published on: November 7, 2020
Strategies to reduce hepatitis C virus recurrence after liver transplantation
Ruben Ciria1, María Pleguezuelo, Shirin Elizabeth Khorsandi
1Ruben Ciria, Shirin Elizabeth Khorsandi, Diego Davila, Abid Suddle, Hector Vilca-Melendez, Nigel Heaton, Institute of Liver Studies, King's College Hospital, London SE5 9RS, United Kingdom.
Insights
Hepatitis C virus (HCV) recurrence post-liver transplant is common and accelerates graft damage. Strategies targeting pre-transplant, transplant, and post-transplant phases can mitigate HCV recurrence and improve patient outcomes.
Area of Science:
- Hepatology
- Transplantation Immunology
- Virology
Background:
- Hepatitis C virus (HCV) infection is a leading cause of chronic liver disease, cirrhosis, and hepatocellular carcinoma, frequently necessitating liver transplantation.
- HCV invariably re-infects liver grafts post-transplantation, leading to rapid recurrence, cirrhosis within five years, and poorer patient/graft survival.
- The high rate of HCV recurrence challenges transplant outcomes and graft utilization, prompting research into effective management strategies.
Purpose of the Study:
- To provide a comprehensive overview of post-transplant HCV recurrence.
- To explore strategies for reducing the impact of HCV recurrence on liver transplant recipients.
- To guide clinicians in managing HCV recurrence by examining interventions at different stages of the transplant process.
Main Methods:
- This review synthesizes current literature on Hepatitis C virus recurrence after liver transplantation.
- It analyzes factors influencing recurrence risk, including pre-transplant viral load, donor characteristics, and ischemia-reperfusion injury.
- The review discusses post-transplant management options, focusing on immunosuppression and antiviral therapy timing.
Main Results:
- HCV recurrence post-liver transplant is nearly universal and associated with accelerated graft damage and cirrhosis.
- Factors such as donor age, graft steatosis, and ischemia/reperfusion injury may increase recurrence severity.
- Optimizing immunosuppression and timing of antiviral treatment (prophylactic, pre-emptive, or on-demand) are key areas for intervention.
Conclusions:
- Effective management of HCV recurrence is crucial for improving outcomes in liver transplant recipients.
- Interventions targeting pre-transplant, peri-transplant, and post-transplant periods hold promise for reducing recurrence impact.
- Further research is needed to establish long-term benefits of pre-transplant viral load reduction and optimize post-transplant treatment protocols.
Abstract:
Hepatitis C virus (HCV) is a major health problem that leads to chronic hepatitis, cirrhosis and hepatocellular carcinoma, being the most frequent indication for liver transplantation in several countries. Unfortunately, HCV re-infects the liver graft almost invariably following reperfusion, with an accelerated history of recurrence, leading to 10%-30% of patients progressing to cirrhosis within 5 years of transplantation. In this sense, some groups have even advocated for not re-transplanting this patients, as lower patient and graft outcomes have been reported. However, the management of HCV recurrence is being optimized and several strategies to reduce post-transplant recurrence could improve outcomes, decrease the rate of re-transplantation and optimize the use of available grafts. Three moments may be the focus of potential actions in order to decrease the impact of viral recurrence: the pre-transplant moment, the transplant environment and the post-transplant management. In the pre-transplant setting, it is not well established if reducing the pre transplant viral load affects the risk for HCV progression after transplant. Obviously, antiviral treatment can render the patient HCV RNA negative post transplant but the long-term benefit has not yet been fully established to justify the cost and clinical risk. In the transplant moment, factors as donor age, cold ischemia time, graft steatosis and ischemia/reperfusion injury may lead to a higher and more aggressive viral recurrence. After the transplant, discussion about immunosuppression and the moment to start the treatment (prophylactic, pre-emptive or once-confirmed) together with new antiviral drugs are of interest. This review aims to help clinicians have a global overview of post-transplant HCV recurrence and strategies to reduce its impact on our patients.
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