Transplant Tolerance, Not Only Clonal Deletion

The quest to understand how allogeneic transplanted tissue is not rejected and how tolerance is induced led to fundamental concepts in immunology. First, we review the research that led to the Clonal Deletion theory in the late 1950s that has since dominated the field of immunology and transplantati...

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Main Authors: Bruce M. Hall, Nirupama D. Verma, Giang T. Tran, Suzanne J. Hodgkinson
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.810798/full
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author Bruce M. Hall
Nirupama D. Verma
Giang T. Tran
Suzanne J. Hodgkinson
author_facet Bruce M. Hall
Nirupama D. Verma
Giang T. Tran
Suzanne J. Hodgkinson
author_sort Bruce M. Hall
collection DOAJ
description The quest to understand how allogeneic transplanted tissue is not rejected and how tolerance is induced led to fundamental concepts in immunology. First, we review the research that led to the Clonal Deletion theory in the late 1950s that has since dominated the field of immunology and transplantation. At that time many basic mechanisms of immune response were unknown, including the role of lymphocytes and T cells in rejection. These original observations are reassessed by considering T regulatory cells that are produced by thymus of neonates to prevent autoimmunity. Second, we review “operational tolerance” induced in adult rodents and larger animals such as pigs. This can occur spontaneously especially with liver allografts, but also can develop after short courses of a variety of rejection inhibiting therapies. Over time these animals develop alloantigen specific tolerance to the graft but retain the capacity to reject third-party grafts. These animals have a “split tolerance” as peripheral lymphocytes from these animals respond to donor alloantigen in graft versus host assays and in mixed lymphocyte cultures, indicating there is no clonal deletion. Investigation of this phenomenon excludes many mechanisms, including anti-donor antibody blocking rejection as well as anti-idiotypic responses mediated by antibody or T cells. This split tolerance is transferred to a second immune-depleted host by T cells that retain the capacity to effect rejection of third-party grafts by the same host. Third, we review research on alloantigen specific inhibitory T cells that led to the first identification of the CD4+CD25+T regulatory cell. The key role of T cell derived cytokines, other than IL-2, in promoting survival and expansion of antigen specific T regulatory cells that mediate transplant tolerance is reviewed. The precise methods for inducing and diagnosing operational tolerance remain to be defined, but antigen specific T regulatory cells are key mediators.
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spelling doaj.art-63316bdc9d1e43d484326c936946be512022-12-22T02:04:01ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-04-011310.3389/fimmu.2022.810798810798Transplant Tolerance, Not Only Clonal DeletionBruce M. HallNirupama D. VermaGiang T. TranSuzanne J. HodgkinsonThe quest to understand how allogeneic transplanted tissue is not rejected and how tolerance is induced led to fundamental concepts in immunology. First, we review the research that led to the Clonal Deletion theory in the late 1950s that has since dominated the field of immunology and transplantation. At that time many basic mechanisms of immune response were unknown, including the role of lymphocytes and T cells in rejection. These original observations are reassessed by considering T regulatory cells that are produced by thymus of neonates to prevent autoimmunity. Second, we review “operational tolerance” induced in adult rodents and larger animals such as pigs. This can occur spontaneously especially with liver allografts, but also can develop after short courses of a variety of rejection inhibiting therapies. Over time these animals develop alloantigen specific tolerance to the graft but retain the capacity to reject third-party grafts. These animals have a “split tolerance” as peripheral lymphocytes from these animals respond to donor alloantigen in graft versus host assays and in mixed lymphocyte cultures, indicating there is no clonal deletion. Investigation of this phenomenon excludes many mechanisms, including anti-donor antibody blocking rejection as well as anti-idiotypic responses mediated by antibody or T cells. This split tolerance is transferred to a second immune-depleted host by T cells that retain the capacity to effect rejection of third-party grafts by the same host. Third, we review research on alloantigen specific inhibitory T cells that led to the first identification of the CD4+CD25+T regulatory cell. The key role of T cell derived cytokines, other than IL-2, in promoting survival and expansion of antigen specific T regulatory cells that mediate transplant tolerance is reviewed. The precise methods for inducing and diagnosing operational tolerance remain to be defined, but antigen specific T regulatory cells are key mediators.https://www.frontiersin.org/articles/10.3389/fimmu.2022.810798/fullclonal deletiongraft versus host diseasetransplant toleranceregulatory T (Treg) cellschimerism
spellingShingle Bruce M. Hall
Nirupama D. Verma
Giang T. Tran
Suzanne J. Hodgkinson
Transplant Tolerance, Not Only Clonal Deletion
Frontiers in Immunology
clonal deletion
graft versus host disease
transplant tolerance
regulatory T (Treg) cells
chimerism
title Transplant Tolerance, Not Only Clonal Deletion
title_full Transplant Tolerance, Not Only Clonal Deletion
title_fullStr Transplant Tolerance, Not Only Clonal Deletion
title_full_unstemmed Transplant Tolerance, Not Only Clonal Deletion
title_short Transplant Tolerance, Not Only Clonal Deletion
title_sort transplant tolerance not only clonal deletion
topic clonal deletion
graft versus host disease
transplant tolerance
regulatory T (Treg) cells
chimerism
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.810798/full
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AT nirupamadverma transplanttolerancenotonlyclonaldeletion
AT giangttran transplanttolerancenotonlyclonaldeletion
AT suzannejhodgkinson transplanttolerancenotonlyclonaldeletion