Antagonistic effect of the inflammasome on thymic stromal lymphopoietin expression in the skin.

Détails

ID Serval
serval:BIB_C6ED467319C4
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Antagonistic effect of the inflammasome on thymic stromal lymphopoietin expression in the skin.
Périodique
Journal of Allergy and Clinical Immunology
Auteur⸱e⸱s
Schuepbach-Mallepell S., Philippe V., Brüggen M.C., Watanabe H., Roques S., Baldeschi C., Gaide O.
ISSN
1097-6825 (Electronic)
ISSN-L
0091-6749
Statut éditorial
Publié
Date de publication
2013
Peer-reviewed
Oui
Volume
132
Numéro
6
Pages
1348-1357
Langue
anglais
Notes
Publication types: Journal Article Publication Status: ppublish
Résumé
BACKGROUND: Innate immune sensors control key cytokines that regulate T-cell priming and T-cell fate. This is particularly evident in allergic reactions, which represent ideal systems to study the interplay of innate and adaptive immunity. In patients with contact dermatitis, inflammasome-mediated IL-1 activation is responsible for a TH1 immune response. Surprisingly, the IL-1 signaling pathway was also proposed to control the activation of thymic stromal lymphopoietin (TSLP), a cytokine implicated in development of the TH2 response in patients with atopic dermatitis (AD) and asthma.
OBJECTIVES: We sought to assess the effect of the inflammasome on TSLP expression levels and the development of AD.
METHODS: We studied the effect of the inflammasome activator 2,4-dinitrofluorobenzene, and IL-1β on TSLP mRNA expression levels in mouse and human cell lines (in vitro assays), as well as in live mice and on human skin transplants. We also assessed the effect of 2,4-dinitrofluorobenzene on TSLP and the TH2 response in mice in which the inflammasome and IL-1 signaling pathways were blocked, either genetically or pharmacologically, in 2 models of AD.
RESULTS: We provide in vitro and in vivo evidence that inflammasome activation has an inhibitory role on TSLP mRNA expression and TH2 cell fate in the skin. We also show that solvents influence the activation of TSLP and IL-1β and direct the T-cell fate to a given hapten.
CONCLUSION: Our observations strongly suggest that the TH1 versus TH2 cell fate decision is regulated at multiple levels and starts with innate immune events occurring within peripheral epithelial tissues.
Pubmed
Web of science
Création de la notice
03/01/2014 9:34
Dernière modification de la notice
20/08/2019 15:42
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