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Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis

T follicular helper (Tfh) cells provide help for antigen-specific B cells. We have previously shown that Tfh cell frequency was increased and associated with auto-antibodies in patients with rheumatoid arthritis (RA), suggesting a possible involvement of Tfh cells in its pathogenesis. Mesenchymal st...

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Autores principales: Liu, Rui, Li, Xia, Zhang, Zhuoya, Zhou, Min, Sun, Yue, Su, Dinglei, Feng, Xuebing, Gao, Xiang, Shi, Songtao, Chen, Wanjun, Sun, Lingyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531289/
https://www.ncbi.nlm.nih.gov/pubmed/26259824
http://dx.doi.org/10.1038/srep12777
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author Liu, Rui
Li, Xia
Zhang, Zhuoya
Zhou, Min
Sun, Yue
Su, Dinglei
Feng, Xuebing
Gao, Xiang
Shi, Songtao
Chen, Wanjun
Sun, Lingyun
author_facet Liu, Rui
Li, Xia
Zhang, Zhuoya
Zhou, Min
Sun, Yue
Su, Dinglei
Feng, Xuebing
Gao, Xiang
Shi, Songtao
Chen, Wanjun
Sun, Lingyun
author_sort Liu, Rui
collection PubMed
description T follicular helper (Tfh) cells provide help for antigen-specific B cells. We have previously shown that Tfh cell frequency was increased and associated with auto-antibodies in patients with rheumatoid arthritis (RA), suggesting a possible involvement of Tfh cells in its pathogenesis. Mesenchymal stem cells (MSCs) represent a promising alternative cell therapy for RA by modulating T and B cell activation and proliferation. However, it remains unknown whether MSCs have immunoregulation on Tfh cells. In this paper, we have demonstrated that allogeneic MSCs could suppress Tfh cell differentiation in RA patients partly via the production of indoleamine 2,3-dioxygenase (IDO). IFNγ generated from Tfh cell differentiation system induced IDO expression on MSCs. MSCs transplantation (MSCT) into collagen-induced arthritis (CIA) mice prevented arthritis progression by inhibiting both the number and function of Tfh cells in vivo. These findings reveal a novel suppressive function of MSCs in Tfh cells, which has implication in understanding the underlying mechanisms of the immunotherapeutic effects of MSCs on RA patients.
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spelling pubmed-45312892015-08-12 Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis Liu, Rui Li, Xia Zhang, Zhuoya Zhou, Min Sun, Yue Su, Dinglei Feng, Xuebing Gao, Xiang Shi, Songtao Chen, Wanjun Sun, Lingyun Sci Rep Article T follicular helper (Tfh) cells provide help for antigen-specific B cells. We have previously shown that Tfh cell frequency was increased and associated with auto-antibodies in patients with rheumatoid arthritis (RA), suggesting a possible involvement of Tfh cells in its pathogenesis. Mesenchymal stem cells (MSCs) represent a promising alternative cell therapy for RA by modulating T and B cell activation and proliferation. However, it remains unknown whether MSCs have immunoregulation on Tfh cells. In this paper, we have demonstrated that allogeneic MSCs could suppress Tfh cell differentiation in RA patients partly via the production of indoleamine 2,3-dioxygenase (IDO). IFNγ generated from Tfh cell differentiation system induced IDO expression on MSCs. MSCs transplantation (MSCT) into collagen-induced arthritis (CIA) mice prevented arthritis progression by inhibiting both the number and function of Tfh cells in vivo. These findings reveal a novel suppressive function of MSCs in Tfh cells, which has implication in understanding the underlying mechanisms of the immunotherapeutic effects of MSCs on RA patients. Nature Publishing Group 2015-08-11 /pmc/articles/PMC4531289/ /pubmed/26259824 http://dx.doi.org/10.1038/srep12777 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liu, Rui
Li, Xia
Zhang, Zhuoya
Zhou, Min
Sun, Yue
Su, Dinglei
Feng, Xuebing
Gao, Xiang
Shi, Songtao
Chen, Wanjun
Sun, Lingyun
Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title_full Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title_fullStr Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title_full_unstemmed Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title_short Allogeneic mesenchymal stem cells inhibited T follicular helper cell generation in rheumatoid arthritis
title_sort allogeneic mesenchymal stem cells inhibited t follicular helper cell generation in rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531289/
https://www.ncbi.nlm.nih.gov/pubmed/26259824
http://dx.doi.org/10.1038/srep12777
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