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Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis
OBJECTIVES: This study aimed to investigate the changes in quantity and function of T helper (Th)-like T regulatory (Treg) cell subsets in peripheral blood (PB) and synovial fluid (SF) of rheumatoid arthritis (RA) patients and to understand their relationship with disease activity. METHODS: A total...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114761/ https://www.ncbi.nlm.nih.gov/pubmed/35603149 http://dx.doi.org/10.3389/fimmu.2022.863753 |
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author | Zhang, Rui Miao, Jinlin Zhang, Kui Zhang, Bei Luo, Xing Sun, Haoyang Zheng, Zhaohui Zhu, Ping |
author_facet | Zhang, Rui Miao, Jinlin Zhang, Kui Zhang, Bei Luo, Xing Sun, Haoyang Zheng, Zhaohui Zhu, Ping |
author_sort | Zhang, Rui |
collection | PubMed |
description | OBJECTIVES: This study aimed to investigate the changes in quantity and function of T helper (Th)-like T regulatory (Treg) cell subsets in peripheral blood (PB) and synovial fluid (SF) of rheumatoid arthritis (RA) patients and to understand their relationship with disease activity. METHODS: A total of 86 RA patients and 76 gender and age-matched healthy controls (HC) were enrolled in this study. Th-like Treg frequency and function were determined using flow cytometry. The inhibitory function of Th-like Treg cells was detected using an in vitro co-culture suppression assay. RESULTS: The proportion and absolute number of Th1-like Treg cells from RA PB and RA SF were significantly higher than those of HC PB. In RA SF, the proportions of Treg cells and Th1-like Treg cells were significantly lower in the elevated erythrocyte sedimentation rate or the C-Reactive Protein group, and in the positive groups of anti-CCP antibody and anti-MCV antibody. Additionally, the proportions of Treg cells and Th1-like Treg cells from RA SF were negatively correlated with disease activity. However, the expression levels of CD73 and TGF-β1 in Th1-like Treg cells were decreased, and these Treg cells could not effectively inhibit the proliferation of effector T (Teff) cells. CONCLUSION: Our data indicate that Th1-like Treg cells are the predominant Treg cell subset in RA SF, but their suppressive function is defective. Improving the function of Th1-like Treg cells may control inflammation in joints and provide new strategies for Treg-targeted therapies in RA. |
format | Online Article Text |
id | pubmed-9114761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91147612022-05-19 Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis Zhang, Rui Miao, Jinlin Zhang, Kui Zhang, Bei Luo, Xing Sun, Haoyang Zheng, Zhaohui Zhu, Ping Front Immunol Immunology OBJECTIVES: This study aimed to investigate the changes in quantity and function of T helper (Th)-like T regulatory (Treg) cell subsets in peripheral blood (PB) and synovial fluid (SF) of rheumatoid arthritis (RA) patients and to understand their relationship with disease activity. METHODS: A total of 86 RA patients and 76 gender and age-matched healthy controls (HC) were enrolled in this study. Th-like Treg frequency and function were determined using flow cytometry. The inhibitory function of Th-like Treg cells was detected using an in vitro co-culture suppression assay. RESULTS: The proportion and absolute number of Th1-like Treg cells from RA PB and RA SF were significantly higher than those of HC PB. In RA SF, the proportions of Treg cells and Th1-like Treg cells were significantly lower in the elevated erythrocyte sedimentation rate or the C-Reactive Protein group, and in the positive groups of anti-CCP antibody and anti-MCV antibody. Additionally, the proportions of Treg cells and Th1-like Treg cells from RA SF were negatively correlated with disease activity. However, the expression levels of CD73 and TGF-β1 in Th1-like Treg cells were decreased, and these Treg cells could not effectively inhibit the proliferation of effector T (Teff) cells. CONCLUSION: Our data indicate that Th1-like Treg cells are the predominant Treg cell subset in RA SF, but their suppressive function is defective. Improving the function of Th1-like Treg cells may control inflammation in joints and provide new strategies for Treg-targeted therapies in RA. Frontiers Media S.A. 2022-05-04 /pmc/articles/PMC9114761/ /pubmed/35603149 http://dx.doi.org/10.3389/fimmu.2022.863753 Text en Copyright © 2022 Zhang, Miao, Zhang, Zhang, Luo, Sun, Zheng and Zhu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zhang, Rui Miao, Jinlin Zhang, Kui Zhang, Bei Luo, Xing Sun, Haoyang Zheng, Zhaohui Zhu, Ping Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title | Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title_full | Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title_fullStr | Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title_full_unstemmed | Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title_short | Th1-Like Treg Cells Are Increased But Deficient in Function in Rheumatoid Arthritis |
title_sort | th1-like treg cells are increased but deficient in function in rheumatoid arthritis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114761/ https://www.ncbi.nlm.nih.gov/pubmed/35603149 http://dx.doi.org/10.3389/fimmu.2022.863753 |
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