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“Immune modulation through transient donor chimerism” refers to a transplantation-tolerance strategy where a temporary coexistence of donor-derived and recipient hematopoietic cells is established in the recipient after transplantation. This transient chimerism induces donor-specific immune tolerance by promoting mechanisms such as the expansion of regulatory T cells (Tregs), deletion or anergy of alloreactive T cells, and central/peripheral regulatory processes. Unlike persistent or full chimerism, transient chimerism reduces the risk of graft-versus-host disease while maintaining sufficient immunomodulation to allow for withdrawal or reduced use of immunosuppression in organ transplantation. The process is not a molecular entity but a clinical and immunological state induced by specific conditioning regimens, stem cell or bone marrow infusions, and adjunct immunosuppressive agents.
Homeostatic expansion of regulatory T cells (Tregs); Induction of T cell anergy and exhaustion; Peripheral deletion of donor-reactive T cells; Promotion of donor-specific immune tolerance; Central and peripheral immune regulation
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