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Updated: Jun 8, 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
Myeloid-derived suppressor cells in transplantation
Nahzli Dilek1, Nicolas van Rompaey, Alain Le Moine
1aINSERM, UMR643, France bCHU Nantes, Institut de Transplantation Urologie Néphrologie (ITUN), France cFaculté de Médecine, Université de Nantes, Nantes, France dInstitute for Medical Immunology, Université Libre de Bruxelles, Gosselies, Belgium.
Myeloid-derived suppressor cells (MDSCs) regulate innate and adaptive immunity. Recent studies suggest MDSCs play a role in transplantation immunity, influencing graft rejection and tolerance, but require further investigation.
Area of Science:
- Immunology
- Transplantation Science
Background:
- Myeloid-derived suppressor cells (MDSCs) are immature immune cells with significant regulatory functions.
- MDSCs can suppress anti-tumor immune responses but may also be beneficial in preventing allograft rejection and promoting transplantation tolerance.
- Emerging evidence suggests MDSCs influence innate immunity and may be crucial in managing ischemia-reperfusion injury.
Purpose of the Study:
- To review recent findings on the role of MDSCs in solid-organ transplantation.
- To explore the involvement of MDSCs in experimental models of graft-versus-host disease.
Main Methods:
- Review of recent scientific literature focusing on MDSCs in transplantation.
- Analysis of experimental models related to graft-versus-host disease.
Main Results:
- MDSCs are increasingly recognized as key regulators of both innate and adaptive immunity.
- Studies indicate a potential role for MDSCs in modulating early and late stages of transplantation immunity.
- MDSC activity may be beneficial in suppressing immune responses that lead to allograft rejection.
Conclusions:
- MDSCs are vital physiological regulators of immune responses.
- The role of MDSCs in transplantation immunity is a promising area of research.
- Further mechanistic studies in animal models and human subjects are needed to fully elucidate MDSC function and their interaction with immunosuppressive therapies.
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