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Forkhead box protein-3 (Foxp3)-producing dendritic cells suppress allergic response.

Authors :
Liu XY
Xu LZ
Luo XQ
Geng XR
Liu ZQ
Yang LT
Yang G
Chen S
Liu ZG
Li HB
Yang LT
Luan TG
Yang PC
Source :
Allergy [Allergy] 2017 Jun; Vol. 72 (6), pp. 908-917. Date of Electronic Publication: 2017 Feb 21.
Publication Year :
2017

Abstract

Background: The generation of the tolerogenic dendritic cells (DC) is not fully understood yet. Forkhead box protein-3 (Foxp3) is an important molecule in the immune tolerance. This study tests a hypothesis that DCs express Foxp3, which can be upregulated by Staphylococcal enterotoxin B (SEB).<br />Methods: The expression of Foxp3 by DCs was evaluated by real-time RT-PCR, Western blotting, flow cytometry, and chromatin immunoprecipitation assay.<br />Results: We observed that mice treated with SEB at 0.25-0.5 μg/mouse showed high frequencies of transforming growth factor (TGF)-β-producing CD4 <superscript>+</superscript> T cells and TGF-β-producing DCs in the intestine, while the IL-4 <superscript>+</superscript> CD4 <superscript>+</superscript> T cells and TIM4 <superscript>+</superscript> DCs were dominated in the intestine in mice treated with SEB at 1-10 μg/mouse. Treating DCs with SEB in the culture induced high levels of Foxp3 at the TGF-β promoter locus. The function of Foxp3 was blocked by STAT6 (signal transducer and activator transcription-6); the latter was induced by exposing DCs to SEB in the culture at doses of 100-400 ng/ml. Treating allergic mice with specific immunotherapy (SIT) together with SEB significantly promoted the therapeutic effects on the allergic responses than treating with SIT alone.<br />Conclusion: Dendritic cells have the capacity to express Foxp3, which can be upregulated by exposure to SEB.<br /> (© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1398-9995
Volume :
72
Issue :
6
Database :
MEDLINE
Journal :
Allergy
Publication Type :
Academic Journal
Accession number :
27861999
Full Text :
https://doi.org/10.1111/all.13088