Allograft and recipient tissue injury during cardiac allograft rejection: Evidence from cell-free DNA
Year: 2026
Type: article
Study design: Observational Study
Abstract: Cardiac allograft rejection (AR) is conventionally managed as an allograft disease. However, data from kidney transplant and proinflammatory cytokine studies suggest the occurrence of recipient tissue injury during AR, which remains poorly defined to date and is a recognized risk factor for poor survival. This study hypothesizes that AR is linked to recipient tissue injury, measured as plasma cell-free DNA (cfDNA), a biomarker of tissue injury. This study analyzed genetic and epigenetic signatures to quantify allograft and recipient cfDNA and the tissue sources for AR and stable controls. To provide a mechanistic connection, the study compared cfDNA damage-associated molecular pattern activity between patients with AR and stable controls. Results indicate that both allograft and recipient cfDNA levels increase during AR compared with stable controls. The increased recipient cfDNA levels primarily originated from immune cells, vascular endothelium, hepatocytes, and kidney epithelial cells and correlated with conventional biomarkers of organ dysfunction. In cell culture models, AR-derived cfDNA demonstrated increased damage-associated molecular pattern activity compared with cfDNA from stable controls. These findings suggest that AR is linked to heightened recipient cfDNA levels and an increased risk of recipient organ dysfunction. Future research is warranted to investigate these findings further to improve the management and outcomes of AR.
Authors: Temesgen E. Andargie, Naoko Tsuji, Naoki Hayase, Moon Kyoo Jang, Tom Hill, Hyesik Kong, Ethan Fraser, Tihitina Y. Aytenfisu, Trevor S. Johnston, Andrea L. Cox, Atul Mehta, Ashley Park, Manfred Boehm, Kai Yu, Xin Tian, Peter S.T. Yuen, Neelam Redekar, Andrew H. Karaba, Keyur Shah, Clarence M. Lee, Hannah Valantine, Robert A. Star, Sean Agbor-Enoh
Institutions: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Allergy and Infectious Diseases, Johns Hopkins University, National Cancer Institute, Division of Cancer Epidemiology and Genetics, Virginia Commonwealth University, Howard University, Stanford Medicine, Stanford University, Johns Hopkins Medicine
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,300
OpenAlex ID: W7128916322
