Heart and Lung Transplants from HCV-Infected Donors to Uninfected Recipients

Ann E Woolley1, Steve K Singh1, Hilary J Goldberg1

  • 1From the Divisions of Infectious Diseases (A.E.W., A.E.K., M.E.J., K.C., E.A.H., L.R.B.), Cardiac Surgery (S.K.S., H.R.M.), Thoracic Surgery (S.K.S., H.R.M., A.C., P.C.C.), Pulmonary and Critical Care Medicine (H.J.G.), and Cardiovascular Medicine (M.M.G., M.R.M.), and the Department of Pharmacy (J.F.), Brigham and Women's Hospital, Harvard Medical School (A.E.W., S.K.S., H.J.G., H.R.M., M.M.G., M.R.M., A.C., E.A.H., P.C.C., L.R.B.), Massachusetts College of Pharmacy and Health Sciences (J.F.), the Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute (D.P.H.), and Harvard T.H. Chan School of Public Health (D.P.H.) - all in Boston.

Insights

Hepatitis C virus (HCV) infected donor organs can now be safely transplanted into HCV-negative recipients. A 4-week antiviral regimen effectively prevented HCV infection post-transplant, increasing the donor organ pool.

Area of Science:

  • Transplantation immunology
  • Hepatology
  • Infectious diseases

Background:

  • Hepatitis C virus (HCV) viremia in donors typically precludes organ transplantation.
  • Direct-acting antiviral agents offer potential to expand the donor pool using HCV-viremic donors.
  • Transplanting organs from HCV-viremic donors into HCV-negative recipients is being explored.

Purpose of the Study:

  • To assess the safety and efficacy of transplanting organs from HCV-viremic donors into HCV-negative recipients.
  • To evaluate a preemptive antiviral treatment strategy to prevent HCV infection in recipients.
  • To determine the impact on graft survival and viral clearance.

Main Methods:

  • A clinical trial involving heart and lung transplants from HCV-viremic donors to HCV-negative adults.
  • Preemptive administration of sofosbuvir-velpatasvir (a pangenotypic direct-acting antiviral) for 4 weeks post-transplantation.
  • Primary outcome: sustained virologic response at 12 weeks and graft survival at 6 months.

Main Results:

  • 44 patients underwent transplantation (36 lung, 8 heart).
  • 95% of recipients had detectable HCV viral load post-transplant, which became undetectable within 2 weeks.
  • 100% of patients with 6-month follow-up achieved sustained virologic response and excellent graft survival with no serious adverse events.

Conclusions:

  • A 4-week antiviral regimen initiated shortly after transplantation effectively prevents HCV infection in recipients of organs from HCV-viremic donors.
  • This strategy significantly expands the donor organ pool.
  • The approach is safe and highly effective in achieving viral clearance and graft survival.
Abstract

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