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Updated: Jan 19, 2026

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Trained immunity in organ transplantation
Jordi Ochando1,2, Zahi A Fayad3, Joren C Madsen4
1Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.
Trained immunity, a function of the innate immune system, may drive organ transplant rejection. Understanding macrophage reprogramming in trained immunity is key to improving long-term graft survival and reducing immunosuppression toxicity.
Area of Science:
- Immunology
- Transplantation Science
Background:
- Achieving lasting donor-specific unresponsiveness without continuous immunosuppression is a major challenge in organ transplantation.
- Current strategies targeting adaptive immunity show suboptimal long-term graft survival, indicating other rejection mechanisms exist.
Purpose of the Study:
- To explore the role of trained immunity pathways in mediating allograft rejection.
- To summarize the negative impacts of trained immunity in organ transplantation and identify pathways inducing macrophage training.
Main Methods:
- Review of existing literature on trained immunity and its components.
- Analysis of macrophage reprogramming (epigenetic and metabolic) in the context of transplantation.
Main Results:
- Trained immunity, involving epigenetic and metabolic reprogramming of macrophages, contributes to graft rejection.
- Trained macrophages enhance immune responses by upregulating costimulatory molecules and producing pro-inflammatory cytokines.
Conclusions:
- Trained immunity pathways represent a critical, yet often unrecognized, mechanism contributing to organ transplant rejection.
- Targeting trained immunity in macrophages may offer novel therapeutic strategies to improve graft survival and reduce reliance on immunosuppression.
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