Abstract | BACKGROUND: Human regulatory T cells (Tregs) are a heterogeneous population which consists of three distinct subpopulations: CD25+CD45RA+ resting Treg (rTreg) cells; CD25hiCD45RA- activated Treg (aTreg) cells, which are both suppressive; and CD25+CD45RA- cytokine-secreting T cells with pro-inflammatory capacity. OBJECTIVE: We investigated variation in peripheral Treg subpopulations of asthma and explored their potential roles in asthma inflammation. METHODS: Twenty-eight mild asthma patients, 26 moderate asthma patients, 18 severe asthma patients, and 36 healthy controls were recruited for a cross-sectional study. Phenotyping of peripheral CD4+ Tregs was performed based on flow cytometry results. RESULTS: The proportions of rTreg and aTreg cells among CD4+ T cells were higher in mild and moderate asthma patients than in healthy controls. All three groups of asthmatics had a higher proportion of pro-inflammatory Tregs than healthy controls, and these increased with asthma severity. The proportion of IL-17-producing Foxp3+ cells and IFN-ɤ-producing Foxp3+ cells strongly correlated with T helper 17 (Th17) cells (r = 0.66, p < 0.001) and Th1 cells (r = 0.48, p < 0.001). The pro-inflammatory Treg subpopulation was correlated with the severity of asthma and may be insensitive to corticosteroids. CONCLUSIONS: Our data suggest that pro-inflammatory Treg subpopulations may be relevant to the plasticity of Th17 and Th1 differentiation and play an important role in the pathogenesis of asthma.
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Authors | Lei Xin, Junjie Gao, Xiahui Ge, Chenxuan Tian, Weirong Ma, Zhigang Tian, Xiwei Zheng, Jia Hou |
Journal | Respiratory medicine
(Respir Med)
Vol. 143
Pg. 129-138
(10 2018)
ISSN: 1532-3064 [Electronic] England |
PMID | 30261984
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2018. Published by Elsevier Ltd. |
Chemical References |
- Cytokines
- Inflammation Mediators
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Topics |
- Adult
- Asthma
(etiology, immunology)
- Cell Plasticity
- Cross-Sectional Studies
- Cytokines
(metabolism)
- Female
- Humans
- Inflammation Mediators
(metabolism)
- Male
- Middle Aged
- Severity of Illness Index
- T-Lymphocytes, Regulatory
(metabolism)
- Th1 Cells
(physiology)
- Th17 Cells
(physiology)
- Young Adult
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