Abstract |
Previous studies have demonstrated that activation/expansion by certain cytokines as well as recruitment by specific chemokines is involved in enrichment of regulatory T (Treg) cells in local tissues or organs under pathological conditions. Recent evidence indicates that human Treg cells are a heterogeneous population that comprises three distinct subpopulations: CD25⁺CD45RA⁺ resting Treg (rTreg) cells, CD25(hi)CD45RA⁻ activated Treg (aTreg) cells, which are both suppressive, and CD25⁺CD45RA⁻ cytokine-secreting T cells with proinflammatory capacity. Moreover, rTreg cells can proliferate and convert to aTreg cells. Here, we found an increase in aTreg-cell frequency in the cerebrospinal fluid (CSF) of patients with postneurosurgery bacterial meningitis. We revealed that such an increased aTreg-cell frequency in the CSF was not due to enhanced chemotaxis. Instead of a classic conversion pathway from rTreg to aTreg cells, we identified an alternative route of Treg-cell conversion from cytokine-secreting cells to aTreg cells induced by myeloid-specific chemokine CXC chemokine receptor (CXCR) ligand 5 via CXCR1 and CXCR2 receptors, or by CSF myeloid cells in a cell-cell contact manner. Our results reveal a different view of how the immune system controls overwhelming local immune responses during infection, and provide evidence of how innate immunity negatively regulates adaptive immunity.
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Authors | Guangzhi Shi, Junyan Han, Gang Liu, Yu Hao, Yaluan Ma, Tong Li, Xueying Wu, Henghui Zhang, Yanan Liu, Beibei Wang, Yaxian Kong, Jianxin Zhou, Hui Zeng |
Journal | European journal of immunology
(Eur J Immunol)
Vol. 44
Issue 2
Pg. 420-30
(Feb 2014)
ISSN: 1521-4141 [Electronic] Germany |
PMID | 24155161
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Receptors, Chemokine
- Transforming Growth Factor beta
|
Topics |
- Adult
- Cerebrospinal Fluid
(immunology)
- Chemotaxis
(immunology)
- Female
- Granulocytes
(immunology)
- Humans
- Male
- Meningitis, Bacterial
(immunology)
- Myeloid Cells
(immunology)
- Receptors, Chemokine
(immunology)
- T-Lymphocytes, Regulatory
(immunology)
- Transforming Growth Factor beta
(immunology)
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