Related Experiment Video
Updated: Sep 4, 2025

Establishment of the Dual Humanized TK-NOG Mouse Model for HIV-associated Liver Pathogenesis
Published on: September 11, 2019
Donors with human immunodeficiency virus and hepatitis C virus for solid organ transplantation: what's new
Stephanie A Lushniak1, Christine M Durand
1Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Insights
Organ transplantation from donors with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) is now safe and effective. These expanded donor options improve patient survival and reduce organ waitlist mortality.
Area of Science:
- Organ transplantation
- Infectious disease research
- Public health policy
Background:
- The HOPE Act and direct-acting antiviral (DAA) therapies have expanded organ donor criteria.
- Donors with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) are now viable for transplantation.
- This expands opportunities for patients on organ waitlists.
Purpose of the Study:
- To provide updates on recent studies in solid organ transplantation (SOT) using donors with HIV and HCV.
- To evaluate the safety and efficacy of using organs from HIV- and HCV-positive donors.
- To assess the impact on organ availability and waitlist mortality.
Main Methods:
- Review of pilot studies and clinical outcomes in SOT from HIV-positive donors to HIV-positive recipients (HIV D+/R+).
- Analysis of transplantation outcomes using HCV-positive donors (HCV D+) in recipients without HCV (HCV D-/R-), with DAA therapy.
- Inclusion of both abdominal and thoracic transplantation data.
Main Results:
- HIV D+/R+ kidney and liver transplantation shows robust patient survival and comparable graft survival to standard donors.
- No increased rates of HIV breakthrough were observed in HIV D+/R+ recipients.
- Transplantation using HCV D+/R- donors with DAAs demonstrates excellent outcomes in both abdominal and thoracic SOT.
- Utilization of HIV D+ organs has been lower than anticipated.
Conclusions:
- Transplantation from HIV D+/R+ donors is a safe and effective clinical option.
- Transplantation from HCV D+/R- donors with DAAs shows excellent outcomes.
- These practices support mitigating organ shortage and reducing waitlist mortality.
Purpose Of The Review:
Passage of the HOPE Act and the advent of direct-acting antiviral (DAA) therapies have allowed for expansion of the donor organ pool to include donors with human immunodeficiency virus (HIV) and hepatitis C virus (HCV), thus providing new opportunities for waitlist candidates. This article provides updates on recent studies in solid organ transplantation (SOT) utilizing donors with HIV and HCV.
Recent Findings:
The first pilot studies of kidney and liver transplantation from donors-with-HIV to recipients-with-HIV (HIV D+/R+) show robust patient survival, comparable graft survival to transplantation from donors without HIV (HIV D-/R+) and no increased rates of HIV breakthrough. The number of HIV D+ organs utilized has been lower than initial estimates due to several potential factors. With high numbers of overdose deaths from the opioid epidemic, there have been more HCV D+ organs available, leading to transplantation in recipients without HCV (HCV D+/R-) in combination with DAAs. Outcomes in both abdominal and thoracic HCV D+/R transplantation are excellent.
Summary:
With recent findings of good outcomes in both HIV D+/R+ and HCV D+/R- SOT, we feel the evidence supports both practices as standard clinical care options to mitigate organ shortage and reduce waitlist mortality.
More Related Videos
Related Concept Videos
Kidney Transplant I: Introduction
Tissue Transplantation
The Biology of Tissue Transplantation
The biology of tissue transplantation hinges on the Major Histocompatibility Complex (MHC) molecules. These molecules...
Immunodeficiency Diseases
There are three main causes of immunodeficiency...
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy...
Sexually Transmitted Infections

