Related Experiment Video
Updated: Oct 1, 2025

Heterotopic Auxiliary Whole Liver Rat Transplant Model Utilizing a Hepaticoureterostomy for Allograft Rejection Studies
Published on: March 8, 2024
Utilization of HCV viremic donors in kidney transplantation: a chance or a threat?
Paulina Czarnecka1, Kinga Czarnecka1, Olga Tronina1
1Department of Transplant Medicine, Nephrology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.
Insights
Using hepatitis C virus (HCV) viremic organs for kidney transplants can increase organ availability. While effective, long-term outcomes of transplanting HCV Nucleic Acid Testing positive (NAT+) donor kidneys to naive recipients require further study.
Area of Science:
- Nephrology
- Transplantation immunology
- Infectious diseases
Background:
- Kidney transplantation is the preferred treatment for end-stage renal disease.
- Organ shortage limits kidney transplant utilization.
- Direct-acting antivirals (DAAs) enable transplantation of organs from hepatitis C virus (HCV) viremic donors.
Purpose of the Study:
- To review the use of HCV Nucleic Acid Testing positive (NAT+) donor organs for kidney transplantation.
- To analyze the possibilities and limitations of utilizing HCV NAT+ donor organs in naive recipients.
Main Methods:
- Literature review of studies on HCV NAT+ donor kidney transplantation.
- Analysis of outcomes, rejection rates, and long-term consequences.
- Examination of current knowledge on HCV viremia as a factor in organ rejection.
Main Results:
- HCV NAT+ donor kidneys can be safely transplanted to naive recipients, increasing organ availability.
- Organs from HCV viremic donors are rejected more frequently than those from HCV-negative donors, primarily due to viremia.
- DAAs have improved the efficacy of treating HCV infection post-transplant.
Conclusions:
- Transplanting HCV NAT+ donor kidneys to naive recipients is a viable strategy to address organ scarcity.
- While short-term outcomes are promising, long-term consequences need further investigation.
- HCV viremia, not organ quality, is the main driver of increased rejection rates.
Abstract:
Kidney transplantation is the treatment of choice in end-stage renal disease. The main issue which does not allow to utilize it fully is the number of organs available for transplant. Introduction of highly effective oral direct-acting antivirals (DAAs) to the treatment of chronic hepatitis C virus infection (HCV) enabled transplantation of HCV viremic organs to naive recipients. Despite an increasing number of reports on the satisfying effects of using HCV viremic organs, including kidneys, they are more often rejected than those from HCV negative donors. The main reason is the presence of HCV viremia and not the quality of the organ. The current state of knowledge points to the fact that a kidney transplant from an HCV nucleic acid testing positive (NAT+) donor to naive recipients is an effective and safe solution to the problem of the insufficient number of organs available for transplantation. It does not, however, allow to draw conclusions as to the long-term consequence of such an approach. This review analyzes the possibilities and limitations of the usage of HCV NAT + donor organs. Abbreviations: DAA: direct-acting antivirals; HCV: hepatitis C virus; NAT: nucleic acid testing; OPTN: Organ Procurement and Transplantation Network; KDIGO: Kidney Disease: Improving Global Outcomes; Ab: antigen; eGFR: estimated glomerular filtration rate; D: donor; R: recipient; CMV: cytomegalovirus; HBV: hepatitis B virus; UNOS: United Network for Organ Sharing; PHS: Public Health Service; EBR/GZR: elbasvir/grazoprevir; SVR: sustained virologic response; RAS: resistance-associated substitutions; SOF: soforbuvir; GLE/PIB: glecaprevir/pibrentasvir; ACR: acute cellular rejection; AR: acute rejection; DSA: donor-specific antibodies; KTR: kidney transplant recipients; AASLD: American Association for the Study of Liver Disease; IDSA: Infectious Diseases Society of America; PPI: proton pump inhibitors; CKD: chronic kidney disease; GN: glomerulonephritis; KAS: The Kidney Allocation system.
More Related Videos
Related Concept Videos
Kidney Transplant I: Introduction
Kidney Transplant II: Surgical Procedure
Hemodialysis I: Introduction
Kidney Transplant III: Nursing Management
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy...
Tissue Transplantation
The Biology of Tissue Transplantation
The biology of tissue transplantation hinges on the Major Histocompatibility Complex (MHC) molecules. These molecules...

