Mechanisms of donor-specific transfusion tolerance: preemptive induction of clonal T-cell exhaustion via indirect presentation

Author:

Quezada Sergio A.1,Fuller Bruce1,Jarvinen Lamis Z.1,Gonzalez Mercedes1,Blazar Bruce R.1,Rudensky Alexander Y.1,Strom Terry B.1,Noelle Randolph J.1

Affiliation:

1. From the Department of Microbiology & Immunology, Dartmouth Medical School, Lebanon, NH; the Division of Bone Marrow Transplantation, University of Minnesota, Minneapolis, MN; the Howard Hughes Institute, University of Washington, Seattle, WA; and the Beth Israel Deaconess Medical Center, Department of Medicine, Harvard, Boston, MA.

Abstract

AbstractInduction of transplantation tolerance to alloantigens without general immunosuppression remains an enduring challenge. Injecting a donor-specific transfusion (DST) of spleen cells together with blocking αCD154 antibody prior to graft transplantation is an effective way to induce long-lived graft acceptance. Using a novel T-cell receptor (TCR) transgenic (Tg) model of CD4+ T-cell–mediated rejection, this study sheds new insights into the cellular basis for enhanced graft survival induced by DST and αCD154. The study shows that DST and αCD154 induce an early, robust, abortive expansion of the Tg T cells that results in profound anergy. This is contrasted with the more delayed, regional, productive response elicited by an allogeneic graft. Studies show that the induction of tolerance to the allograft induced by DST is mediated by indirect presentation by host antigen-presenting cells. Based on these observations, we conclude that DST and αCD154 preemptively tolerize the alloreactive T-cell compartment to prohibit subsequent responses to the immunogenic allograft.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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