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Author Spotlight: Enhancing Donor Heart Preservation Through Isolated Rat Heart Perfusion Studies
Published on: October 4, 2024
Outcomes of heart transplantation from hepatitis C virus-positive donors
Saima Aslam1, Ily Yumul2, Mark Mariski3
1Department of Medicine, Division of Infectious Diseases and Global Public Health, University of California, San Diego, San Diego, California, USA.
Insights
Using hepatitis C virus (HCV)-positive donor organs for heart transplantation (HT) in HCV-negative patients resulted in 100% HCV transmission from viremic donors, but all infections were successfully treated with direct-acting antiviral agents.
Area of Science:
- Transplantation Medicine
- Infectious Diseases
- Hepatology
Background:
- Increasing organ donation opportunities exist for hepatitis C virus (HCV)-infected individuals.
- HCV+ organs are an underutilized resource in organ transplantation.
Purpose of the Study:
- To evaluate the safety and efficacy of using HCV-positive donor organs for heart transplantation (HT) in HCV-negative recipients.
- To assess HCV transmission rates and treatment outcomes in recipients of HCV+ donor hearts.
Main Methods:
- Developed a clinical practice protocol for accepting HCV+ organs for HCV- recipients undergoing HT.
- Retrospectively reviewed outcomes of 21 patients who received HT from HCV+ donors.
- Monitored HCV transmission, viral load, and treatment response with direct-acting antiviral (DAA) agents.
Main Results:
- 21 HCV+ donor hearts were transplanted into HCV- recipients.
- 100% HCV transmission occurred in recipients of viremic HCV+ donors (19/19).
- All 19 infected recipients achieved sustained virologic response after 12 weeks of DAA therapy.
Conclusions:
- Utilizing HCV+ organs for HT in HCV- recipients is feasible and expands the donor pool.
- DAA therapy is highly effective in treating HCV infection post-transplantation.
- Further long-term follow-up is necessary to confirm the durability of treatment outcomes.
Background:
National data demonstrate that increasing opportunities exist for organ donation among hepatitis C virus (HCV)-infected individuals.
Methods:
We developed a clinical practice protocol for the acceptance of HCV+ organs for HCV- patients who underwent heart transplantation (HT) and retrospectively reviewed the outcomes at our institution. Inclusion criteria were as follows: all adult patients listed for HT. Exclusion criteria were as follows: pre-existing HIV or active hepatitis B viremia in the recipient/donor.
Results:
We transplanted 21 patients from HCV+ donors. Nineteen were viremic donors, and 2 were non-viremic donors. The recipients included 18 patients who underwent HT alone, and 3 patients who underwent combined heart-kidney transplants. There was no HCV transmission from the non-viremic donors (n = 2). All 19 recipients of the viremic donors developed HCV infection (100% transmission). The median age of the viremic donors was 34 years (interquartile range 30-46), and 84.2% were considered US Public Health Service-increased risk. Induction immunosuppression consisted of anti-thymocyte globulin (7/21), basiliximab (7/21), or none (8/21). Maintenance immunosuppression comprised tacrolimus, mycophenolate mofetil, and prednisone. Post-operative Week 2 HCV viral load was not related to induction. Direct anti-viral agent (DAA) therapy for a 12-week course consisted of glecaprevir/pibrentasvir (14/19, 74%), sofosbuvir/velpatasvir (2/19, 11%), elbasvir/grazoprevir (2/19, 11%), and ledipasvir/sofosbuvir (1/19, 5%). All the patients on DAA therapy cleared viremia. The sustained virological response rate at 12 weeks in 18 evaluable patients was 100%.
Conclusions:
We report successful single-center experience using HCV+ organs for HT into HCV- recipients. We believe that there is utility in using such organs to expand the current donor pool. Further long-term follow-up is needed.
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