Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells

Abstract Resting and activated subpopulations of CD4+CD25+CD127loT regulatory cells (Treg) and CD4+CD25+CD127+ effector T cells in MS patients and in healthy individuals were compared. Peripheral blood mononuclear cells isolated using Ficoll Hypaque were stained with monoclonal antibodies and analys...

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Main Authors: Nirupama D. Verma, Andrew D. Lam, Christopher Chiu, Giang T. Tran, Bruce M. Hall, Suzanne J. Hodgkinson
Format: Article
Language:English
Published: Nature Portfolio 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-88448-5
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author Nirupama D. Verma
Andrew D. Lam
Christopher Chiu
Giang T. Tran
Bruce M. Hall
Suzanne J. Hodgkinson
author_facet Nirupama D. Verma
Andrew D. Lam
Christopher Chiu
Giang T. Tran
Bruce M. Hall
Suzanne J. Hodgkinson
author_sort Nirupama D. Verma
collection DOAJ
description Abstract Resting and activated subpopulations of CD4+CD25+CD127loT regulatory cells (Treg) and CD4+CD25+CD127+ effector T cells in MS patients and in healthy individuals were compared. Peripheral blood mononuclear cells isolated using Ficoll Hypaque were stained with monoclonal antibodies and analysed by flow cytometer. CD45RA and Foxp3 expression within CD4+ cells and in CD4+CD25+CD127loT cells identified Population I; CD45RA+Foxp3+, Population II; CD45RA−Foxp3hi and Population III; CD45RA−Foxp3+ cells. Effector CD4+CD127+ T cells were subdivided into Population IV; memory /effector CD45RA− CD25−Foxp3− and Population V; effector naïve CD45RA+CD25−Foxp3−CCR7+ and terminally differentiated RA+ (TEMRA) effector memory cells. Chemokine receptor staining identified CXCR3+Th1-like Treg, CCR6+Th17-like Treg and CCR7+ resting Treg. Resting Treg (Population I) were reduced in MS patients, both in untreated and treated MS compared to healthy donors. Activated/memory Treg (Population II) were significantly increased in MS patients compared to healthy donors. Activated effector CD4+ (Population IV) were increased and the naïve/ TEMRA CD4+ (Population V) were decreased in MS compared to HD. Expression of CCR7 was mainly in Population I, whereas expression of CCR6 and CXCR3 was greatest in Populations II and intermediate in Population III. In MS, CCR6+Treg were lower in Population III. This study found MS is associated with significant shifts in CD4+T cells subpopulations. MS patients had lower resting CD4+CD25+CD45RA+CCR7+ Treg than healthy donors while activated CD4+CD25hiCD45RA−Foxp3hiTreg were increased in MS patients even before treatment. Some MS patients had reduced CCR6+Th17-like Treg, which may contribute to the activity of MS.
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spelling doaj.art-e08842a8d1044209a7ddc91f273c3f392022-12-21T20:36:20ZengNature PortfolioScientific Reports2045-23222021-05-0111111410.1038/s41598-021-88448-5Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cellsNirupama D. Verma0Andrew D. Lam1Christopher Chiu2Giang T. Tran3Bruce M. Hall4Suzanne J. Hodgkinson5Ingham Institute for Applied Medical ResearchIngham Institute for Applied Medical ResearchIngham Institute for Applied Medical ResearchIngham Institute for Applied Medical ResearchIngham Institute for Applied Medical ResearchIngham Institute for Applied Medical ResearchAbstract Resting and activated subpopulations of CD4+CD25+CD127loT regulatory cells (Treg) and CD4+CD25+CD127+ effector T cells in MS patients and in healthy individuals were compared. Peripheral blood mononuclear cells isolated using Ficoll Hypaque were stained with monoclonal antibodies and analysed by flow cytometer. CD45RA and Foxp3 expression within CD4+ cells and in CD4+CD25+CD127loT cells identified Population I; CD45RA+Foxp3+, Population II; CD45RA−Foxp3hi and Population III; CD45RA−Foxp3+ cells. Effector CD4+CD127+ T cells were subdivided into Population IV; memory /effector CD45RA− CD25−Foxp3− and Population V; effector naïve CD45RA+CD25−Foxp3−CCR7+ and terminally differentiated RA+ (TEMRA) effector memory cells. Chemokine receptor staining identified CXCR3+Th1-like Treg, CCR6+Th17-like Treg and CCR7+ resting Treg. Resting Treg (Population I) were reduced in MS patients, both in untreated and treated MS compared to healthy donors. Activated/memory Treg (Population II) were significantly increased in MS patients compared to healthy donors. Activated effector CD4+ (Population IV) were increased and the naïve/ TEMRA CD4+ (Population V) were decreased in MS compared to HD. Expression of CCR7 was mainly in Population I, whereas expression of CCR6 and CXCR3 was greatest in Populations II and intermediate in Population III. In MS, CCR6+Treg were lower in Population III. This study found MS is associated with significant shifts in CD4+T cells subpopulations. MS patients had lower resting CD4+CD25+CD45RA+CCR7+ Treg than healthy donors while activated CD4+CD25hiCD45RA−Foxp3hiTreg were increased in MS patients even before treatment. Some MS patients had reduced CCR6+Th17-like Treg, which may contribute to the activity of MS.https://doi.org/10.1038/s41598-021-88448-5
spellingShingle Nirupama D. Verma
Andrew D. Lam
Christopher Chiu
Giang T. Tran
Bruce M. Hall
Suzanne J. Hodgkinson
Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
Scientific Reports
title Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
title_full Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
title_fullStr Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
title_full_unstemmed Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
title_short Multiple sclerosis patients have reduced resting and increased activated CD4+CD25+FOXP3+T regulatory cells
title_sort multiple sclerosis patients have reduced resting and increased activated cd4 cd25 foxp3 t regulatory cells
url https://doi.org/10.1038/s41598-021-88448-5
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