TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation

Tumor necrosis factor receptor 2 (TNFR2) has been shown to play a crucial role in CD4+ T regulatory cells (CD4+Tregs) expansion and suppressive function. Increasing evidence has also demonstrated its role in a variety of immune regulatory cell subtypes such as CD8+ T regulatory cells (CD8+ Tregs), B...

Full description

Bibliographic Details
Main Authors: Araz Kouyoumdjian, Jean Tchervenkov, Steven Paraskevas
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.903913/full
_version_ 1828465428129644544
author Araz Kouyoumdjian
Araz Kouyoumdjian
Jean Tchervenkov
Jean Tchervenkov
Steven Paraskevas
Steven Paraskevas
author_facet Araz Kouyoumdjian
Araz Kouyoumdjian
Jean Tchervenkov
Jean Tchervenkov
Steven Paraskevas
Steven Paraskevas
author_sort Araz Kouyoumdjian
collection DOAJ
description Tumor necrosis factor receptor 2 (TNFR2) has been shown to play a crucial role in CD4+ T regulatory cells (CD4+Tregs) expansion and suppressive function. Increasing evidence has also demonstrated its role in a variety of immune regulatory cell subtypes such as CD8+ T regulatory cells (CD8+ Tregs), B regulatory cells (Bregs), and myeloid-derived suppressor cells (MDSCs). In solid organ transplantation, regulatory immune cells have been associated with decreased ischemia-reperfusion injury (IRI), improved graft survival, and improved overall outcomes. However, despite TNFR2 being studied in the context of autoimmune diseases, cancer, and hematopoietic stem cell transplantation, there remains paucity of data in the context of solid organ transplantation and islet cell transplantation. Interestingly, TNFR2 signaling has found a clinical application in islet transplantation which could guide its wider use. This article reviews the current literature on TNFR2 expression in immune modulatory cells as well as IRI, cell, and solid organ transplantation. Our results highlighted the positive impact of TNFR2 signaling especially in kidney and islet transplantation. However, further investigation of TNFR2 in all types of solid organ transplantation are required as well as dedicated studies on its therapeutic use during induction therapy or treatment of rejection.
first_indexed 2024-12-11T03:32:47Z
format Article
id doaj.art-7050f161972c42659ed66d11bcff015e
institution Directory Open Access Journal
issn 1664-3224
language English
last_indexed 2024-12-11T03:32:47Z
publishDate 2022-07-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Immunology
spelling doaj.art-7050f161972c42659ed66d11bcff015e2022-12-22T01:22:21ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-07-011310.3389/fimmu.2022.903913903913TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in TransplantationAraz Kouyoumdjian0Araz Kouyoumdjian1Jean Tchervenkov2Jean Tchervenkov3Steven Paraskevas4Steven Paraskevas5Division of Experimental Surgery, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, CanadaDivision of General Surgery, Department of Surgery, McGill University, Montreal, QC, CanadaDivision of Experimental Surgery, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, CanadaDivision of General Surgery, Department of Surgery, McGill University, Montreal, QC, CanadaDivision of Experimental Surgery, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, CanadaDivision of General Surgery, Department of Surgery, McGill University, Montreal, QC, CanadaTumor necrosis factor receptor 2 (TNFR2) has been shown to play a crucial role in CD4+ T regulatory cells (CD4+Tregs) expansion and suppressive function. Increasing evidence has also demonstrated its role in a variety of immune regulatory cell subtypes such as CD8+ T regulatory cells (CD8+ Tregs), B regulatory cells (Bregs), and myeloid-derived suppressor cells (MDSCs). In solid organ transplantation, regulatory immune cells have been associated with decreased ischemia-reperfusion injury (IRI), improved graft survival, and improved overall outcomes. However, despite TNFR2 being studied in the context of autoimmune diseases, cancer, and hematopoietic stem cell transplantation, there remains paucity of data in the context of solid organ transplantation and islet cell transplantation. Interestingly, TNFR2 signaling has found a clinical application in islet transplantation which could guide its wider use. This article reviews the current literature on TNFR2 expression in immune modulatory cells as well as IRI, cell, and solid organ transplantation. Our results highlighted the positive impact of TNFR2 signaling especially in kidney and islet transplantation. However, further investigation of TNFR2 in all types of solid organ transplantation are required as well as dedicated studies on its therapeutic use during induction therapy or treatment of rejection.https://www.frontiersin.org/articles/10.3389/fimmu.2022.903913/fullTNFR2immune regulationtransplantationrejectionischemia reperfusion injury (IRI)
spellingShingle Araz Kouyoumdjian
Araz Kouyoumdjian
Jean Tchervenkov
Jean Tchervenkov
Steven Paraskevas
Steven Paraskevas
TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
Frontiers in Immunology
TNFR2
immune regulation
transplantation
rejection
ischemia reperfusion injury (IRI)
title TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
title_full TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
title_fullStr TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
title_full_unstemmed TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
title_short TFNR2 in Ischemia-Reperfusion Injury, Rejection, and Tolerance in Transplantation
title_sort tfnr2 in ischemia reperfusion injury rejection and tolerance in transplantation
topic TNFR2
immune regulation
transplantation
rejection
ischemia reperfusion injury (IRI)
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.903913/full
work_keys_str_mv AT arazkouyoumdjian tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation
AT arazkouyoumdjian tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation
AT jeantchervenkov tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation
AT jeantchervenkov tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation
AT stevenparaskevas tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation
AT stevenparaskevas tfnr2inischemiareperfusioninjuryrejectionandtoleranceintransplantation