Balancing Inflammation: The Link between Th17 and Regulatory T Cells

CD4+ T cell compartments in mouse and man are composed of multiple distinct subsets each possessing unique phenotypic and functional characteristics. IL-17-producing CD4+ T cells (Th17 cells) represent a distinct subset of the CD4+ T cell lineage. Recent evidence suggests that Th17 cells carry out e...

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Main Authors: Maggie L. Diller, Ragini R. Kudchadkar, Keith A. Delman, David H. Lawson, Mandy L. Ford
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2016/6309219
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author Maggie L. Diller
Ragini R. Kudchadkar
Keith A. Delman
David H. Lawson
Mandy L. Ford
author_facet Maggie L. Diller
Ragini R. Kudchadkar
Keith A. Delman
David H. Lawson
Mandy L. Ford
author_sort Maggie L. Diller
collection DOAJ
description CD4+ T cell compartments in mouse and man are composed of multiple distinct subsets each possessing unique phenotypic and functional characteristics. IL-17-producing CD4+ T cells (Th17 cells) represent a distinct subset of the CD4+ T cell lineage. Recent evidence suggests that Th17 cells carry out effector functions similar to cytotoxic CD8+ T cells and play an important role in the clearance of extracellular pathogens and fungi. Th17 cell differentiation and function are closely related to the development and function of regulatory T cells (TREG). The balance between these two cell populations is essential for immune homeostasis and dysregulation of this balance has been implicated in a variety of inflammatory conditions including autoimmunity, allograft rejection, and tumorigenesis. Emerging evidence reports a significant amount of plasticity between the Th17 and regulatory T cell compartments, and the mechanisms by which these cells communicate and influence each other are just beginning to be understood. In this review, we highlight recent findings detailing the mechanisms driving Th17 and TREG plasticity and discuss the biologic consequences of their unique relationship.
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spelling doaj-art-52c4f3bb18194f1c854fee64384e13d92025-02-03T06:13:59ZengWileyMediators of Inflammation0962-93511466-18612016-01-01201610.1155/2016/63092196309219Balancing Inflammation: The Link between Th17 and Regulatory T CellsMaggie L. Diller0Ragini R. Kudchadkar1Keith A. Delman2David H. Lawson3Mandy L. Ford4Department of Surgery of Emory University, 1364 Clifton Road, Atlanta, GA 30322, USADepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Road No. C, Atlanta, GA 30322, USADepartment of Surgical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Road No. C, Atlanta, GA 30322, USADepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, 1365 Clifton Road No. C, Atlanta, GA 30322, USAEmory Transplant Center of Emory University, 5105 Woodruff Memorial Research Building, 101 Woodruff Circle, Atlanta, GA 30322, USACD4+ T cell compartments in mouse and man are composed of multiple distinct subsets each possessing unique phenotypic and functional characteristics. IL-17-producing CD4+ T cells (Th17 cells) represent a distinct subset of the CD4+ T cell lineage. Recent evidence suggests that Th17 cells carry out effector functions similar to cytotoxic CD8+ T cells and play an important role in the clearance of extracellular pathogens and fungi. Th17 cell differentiation and function are closely related to the development and function of regulatory T cells (TREG). The balance between these two cell populations is essential for immune homeostasis and dysregulation of this balance has been implicated in a variety of inflammatory conditions including autoimmunity, allograft rejection, and tumorigenesis. Emerging evidence reports a significant amount of plasticity between the Th17 and regulatory T cell compartments, and the mechanisms by which these cells communicate and influence each other are just beginning to be understood. In this review, we highlight recent findings detailing the mechanisms driving Th17 and TREG plasticity and discuss the biologic consequences of their unique relationship.http://dx.doi.org/10.1155/2016/6309219
spellingShingle Maggie L. Diller
Ragini R. Kudchadkar
Keith A. Delman
David H. Lawson
Mandy L. Ford
Balancing Inflammation: The Link between Th17 and Regulatory T Cells
Mediators of Inflammation
title Balancing Inflammation: The Link between Th17 and Regulatory T Cells
title_full Balancing Inflammation: The Link between Th17 and Regulatory T Cells
title_fullStr Balancing Inflammation: The Link between Th17 and Regulatory T Cells
title_full_unstemmed Balancing Inflammation: The Link between Th17 and Regulatory T Cells
title_short Balancing Inflammation: The Link between Th17 and Regulatory T Cells
title_sort balancing inflammation the link between th17 and regulatory t cells
url http://dx.doi.org/10.1155/2016/6309219
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AT keithadelman balancinginflammationthelinkbetweenth17andregulatorytcells
AT davidhlawson balancinginflammationthelinkbetweenth17andregulatorytcells
AT mandylford balancinginflammationthelinkbetweenth17andregulatorytcells