IL-10 signaling in dendritic cells is required for tolerance induction in a murine model of allergic airway inflammation.
Allergy
Dendritic cell
IL-10
Immunotherapy
Tolerance
Journal
European journal of immunology
ISSN: 1521-4141
Titre abrégé: Eur J Immunol
Pays: Germany
ID NLM: 1273201
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
27
08
2018
revised:
04
12
2018
accepted:
17
12
2018
pubmed:
20
12
2018
medline:
20
5
2020
entrez:
20
12
2018
Statut:
ppublish
Résumé
Allergen specific tolerance induction efficiently ameliorates subsequent allergen induced inflammatory responses. The underlying regulatory mechanisms have been attributed mainly to interleukin (IL)-10 produced by diverse hematopoietic cells, while targets of IL-10 in allergen specific tolerance induction have not yet been well defined. Here, we investigate potential cellular targets of IL-10 in allergen specific tolerance induction using mice with a cell type specific inactivation of the IL-10 receptor gene. Allergic airway inflammation was effectively prevented by tolerance induction in mice with IL-10 receptor (IL-10R) deficiency in T or B cells. Similarly, IL-10R on monocytes/macrophages and/or neutrophils was not required for tolerance induction. In contrast, tolerance induction was impaired in mice that lack IL-10R on dendritic cells: those mice developed an allergic response characterized by a pronounced neutrophilic lung infiltration, which was not ameliorated by tolerogenic treatment. In conclusion, our results show that allergen specific tolerance can be effectively induced without a direct impact of IL-10 on cells of the adaptive immune system, and highlight dendritic cells, but not macrophages nor neutrophils, as the main target of IL-10 during tolerance induction.
Identifiants
pubmed: 30566244
doi: 10.1002/eji.201847883
doi:
Substances chimiques
IL10 protein, mouse
0
Receptors, Interleukin-10
0
Interleukin-10
130068-27-8
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
302-312Informations de copyright
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.