Diverse Routes of Allograft Tolerance Disruption by Memory T Cells

Memory T lymphocytes constitute a significant problem in tissue and organ transplantation due their contribution to early rejection and their relative resistance to tolerance-promoting therapies. Memory cells generated by environmental antigen exposure, as with T cells in general, harbor a high freq...

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Main Authors: Ronald G. Gill, Adam L. Burrack
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2020.580483/full
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author Ronald G. Gill
Adam L. Burrack
author_facet Ronald G. Gill
Adam L. Burrack
author_sort Ronald G. Gill
collection DOAJ
description Memory T lymphocytes constitute a significant problem in tissue and organ transplantation due their contribution to early rejection and their relative resistance to tolerance-promoting therapies. Memory cells generated by environmental antigen exposure, as with T cells in general, harbor a high frequency of T cell receptors (TCR) spontaneously cross-reacting with allogeneic major histocompatibility complex (MHC) molecules. This phenomenon, known as ‘heterologous’ immunity, is thought to be a key barrier to transplant tolerance induction since such memory cells can potentially react directly with essentially any prospective allograft. In this review, we describe two additional concepts that expand this commonly held view of how memory cells contribute to transplant immunity and tolerance disruption. Firstly, autoimmunity is an additional response that can comprise an endogenously generated form of heterologous alloimmunity. However, unlike heterologous immunity generated as a byproduct of indiscriminate antigen sensitization, autoimmunity can generate T cells that have the unusual potential to interact with the graft either through the recognition of graft-bearing autoantigens or by their cross-reactive (heterologous) alloimmune specificity to MHC molecules. Moreover, we describe an additional pathway, independent of significant heterologous immunity, whereby immune memory to vaccine- or pathogen-induced antigens also may impair tolerance induction. This latter form of immune recognition indirectly disrupts tolerance by the licensing of naïve alloreactive T cells by vaccine/pathogen directed memory cells recognizing the same antigen-presenting cell in vivo. Thus, there appear to be recognition pathways beyond typical heterologous immunity through which memory T cells can directly or indirectly impact allograft immunity and tolerance.
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spelling doaj.art-79ea995a83354d1684419f80bfb936c72022-12-22T01:07:24ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-10-011110.3389/fimmu.2020.580483580483Diverse Routes of Allograft Tolerance Disruption by Memory T CellsRonald G. Gill0Adam L. Burrack1Departments of Surgery and Immunology and Microbiology, University of Colorado Denver, Aurora, CO, United StatesDepartment of Microbiology and Immunology, University of Minnesota Medical School, Minneapolis, MN, United StatesMemory T lymphocytes constitute a significant problem in tissue and organ transplantation due their contribution to early rejection and their relative resistance to tolerance-promoting therapies. Memory cells generated by environmental antigen exposure, as with T cells in general, harbor a high frequency of T cell receptors (TCR) spontaneously cross-reacting with allogeneic major histocompatibility complex (MHC) molecules. This phenomenon, known as ‘heterologous’ immunity, is thought to be a key barrier to transplant tolerance induction since such memory cells can potentially react directly with essentially any prospective allograft. In this review, we describe two additional concepts that expand this commonly held view of how memory cells contribute to transplant immunity and tolerance disruption. Firstly, autoimmunity is an additional response that can comprise an endogenously generated form of heterologous alloimmunity. However, unlike heterologous immunity generated as a byproduct of indiscriminate antigen sensitization, autoimmunity can generate T cells that have the unusual potential to interact with the graft either through the recognition of graft-bearing autoantigens or by their cross-reactive (heterologous) alloimmune specificity to MHC molecules. Moreover, we describe an additional pathway, independent of significant heterologous immunity, whereby immune memory to vaccine- or pathogen-induced antigens also may impair tolerance induction. This latter form of immune recognition indirectly disrupts tolerance by the licensing of naïve alloreactive T cells by vaccine/pathogen directed memory cells recognizing the same antigen-presenting cell in vivo. Thus, there appear to be recognition pathways beyond typical heterologous immunity through which memory T cells can directly or indirectly impact allograft immunity and tolerance.https://www.frontiersin.org/article/10.3389/fimmu.2020.580483/fullimmune memoryautoimmunitytolerancetransplantationinfectionvaccination
spellingShingle Ronald G. Gill
Adam L. Burrack
Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
Frontiers in Immunology
immune memory
autoimmunity
tolerance
transplantation
infection
vaccination
title Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
title_full Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
title_fullStr Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
title_full_unstemmed Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
title_short Diverse Routes of Allograft Tolerance Disruption by Memory T Cells
title_sort diverse routes of allograft tolerance disruption by memory t cells
topic immune memory
autoimmunity
tolerance
transplantation
infection
vaccination
url https://www.frontiersin.org/article/10.3389/fimmu.2020.580483/full
work_keys_str_mv AT ronaldggill diverseroutesofallografttolerancedisruptionbymemorytcells
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