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TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway
BACKGROUND: Even though thymic stromal lymphopoietin (TSLP) has been implicated in the development of allergic inflammation, its influence on immune tolerance mediated by regulatory T cells (Treg) have not been explored. We aimed to dissect the influence of TSLP on immunosuppressive activities of Tr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161393/ https://www.ncbi.nlm.nih.gov/pubmed/20230634 http://dx.doi.org/10.1186/1710-1492-6-4 |
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author | Nguyen, Khoa D Vanichsarn, Christopher Nadeau, Kari C |
author_facet | Nguyen, Khoa D Vanichsarn, Christopher Nadeau, Kari C |
author_sort | Nguyen, Khoa D |
collection | PubMed |
description | BACKGROUND: Even though thymic stromal lymphopoietin (TSLP) has been implicated in the development of allergic inflammation, its influence on immune tolerance mediated by regulatory T cells (Treg) have not been explored. We aimed to dissect the influence of TSLP on immunosuppressive activities of Treg and its potential consequences in human allergic asthma. METHODS: In vitro culture system was utilized to study the effects of TSLP on human Treg. The functional competency of pulmonary Treg from a cohort of 15 allergic asthmatic, 15 healthy control, and 15 non-allergic asthmatic subjects was also evaluated by suppression assays and flow cytometric analysis. RESULTS: Activated pulmonary Treg expressed TSLP-R and responded to TSLP-mediated activation of STAT5. TSLP directly and selectively impaired IL-10 production of Treg and inhibited their suppressive activity. In human allergic asthma, pulmonary Treg exhibited a significant decrease in suppressive activity and IL-10 production compared to healthy control and non-allergic asthmatic counterparts. These functional alterations were associated with elevated TSLP expression in bronchoaveolar lavage fluid (BAL) of allergic asthmatic subjects. Furthermore, allergic asthmatic BAL could suppress IL-10 production by healthy control pulmonary Treg in a TSLP-dependent manner. CONCLUSIONS: These results provide the first evidences for a direct role of TSLP in the regulation of suppressive activities of Treg. TSLP mediated inhibition of Treg function might present a novel pathologic mechanism to dampen tolerogenic immune responses in inflamed asthmatic airway. |
format | Online Article Text |
id | pubmed-3161393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31613932011-08-26 TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway Nguyen, Khoa D Vanichsarn, Christopher Nadeau, Kari C Allergy Asthma Clin Immunol Research BACKGROUND: Even though thymic stromal lymphopoietin (TSLP) has been implicated in the development of allergic inflammation, its influence on immune tolerance mediated by regulatory T cells (Treg) have not been explored. We aimed to dissect the influence of TSLP on immunosuppressive activities of Treg and its potential consequences in human allergic asthma. METHODS: In vitro culture system was utilized to study the effects of TSLP on human Treg. The functional competency of pulmonary Treg from a cohort of 15 allergic asthmatic, 15 healthy control, and 15 non-allergic asthmatic subjects was also evaluated by suppression assays and flow cytometric analysis. RESULTS: Activated pulmonary Treg expressed TSLP-R and responded to TSLP-mediated activation of STAT5. TSLP directly and selectively impaired IL-10 production of Treg and inhibited their suppressive activity. In human allergic asthma, pulmonary Treg exhibited a significant decrease in suppressive activity and IL-10 production compared to healthy control and non-allergic asthmatic counterparts. These functional alterations were associated with elevated TSLP expression in bronchoaveolar lavage fluid (BAL) of allergic asthmatic subjects. Furthermore, allergic asthmatic BAL could suppress IL-10 production by healthy control pulmonary Treg in a TSLP-dependent manner. CONCLUSIONS: These results provide the first evidences for a direct role of TSLP in the regulation of suppressive activities of Treg. TSLP mediated inhibition of Treg function might present a novel pathologic mechanism to dampen tolerogenic immune responses in inflamed asthmatic airway. BioMed Central 2010-03-15 /pmc/articles/PMC3161393/ /pubmed/20230634 http://dx.doi.org/10.1186/1710-1492-6-4 Text en Copyright ©2010 Nguyen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Nguyen, Khoa D Vanichsarn, Christopher Nadeau, Kari C TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title | TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title_full | TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title_fullStr | TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title_full_unstemmed | TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title_short | TSLP directly impairs pulmonary Treg function: association with aberrant tolerogenic immunity in asthmatic airway |
title_sort | tslp directly impairs pulmonary treg function: association with aberrant tolerogenic immunity in asthmatic airway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161393/ https://www.ncbi.nlm.nih.gov/pubmed/20230634 http://dx.doi.org/10.1186/1710-1492-6-4 |
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