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Mast cells are key promoters of contact allergy that mediate the adjuvant effects of haptens
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4507598
Author(s) Dudeck, Anne; Dudeck, Jan; Scholten, Julia; Petzold, Anke; Surianarayanan, Sangeetha; Köhler, Anja; Peschke, Katrin; Vöhringer, David; Waskow, Claudia; Krieg, Thomas; Müller, Werner; Waisman, Ari; Hartmann, Karin; Gunzer, Matthias; Roers, Axel
Author(s) at UniBasel Hartmann, Karin
Year 2011
Title Mast cells are key promoters of contact allergy that mediate the adjuvant effects of haptens
Journal Immunity
Volume 34
Number 6
Pages / Article-Number 973-84
Mesh terms Adjuvants, Immunologic, pharmacology; Animals; Cell Movement; Dendritic Cells, immunology; Dermatitis, Allergic Contact, immunology; Haptens, immunology; Histamine, immunology; Hypertrophy, immunology; Immunity, Innate; Lymph Nodes, immunology; Mast Cells, drug effects, immunology; Mice; Mice, Inbred C57BL; Mutation; Neovascularization, Pathologic, chemically induced, immunology
Abstract A prominent feature of sensitizing environmental compounds that cause allergic contact dermatitis is the rapid induction of an innate inflammatory response that seems to provide danger signals for efficient T cell priming. We generated mouse models of mast cell deficiency, mast cell-specific gene inactivation, and mast cell reporter mice for intravital imaging and showed that these adjuvant effects of contact allergens are mediated by mast cells and histamine. Mast cell deficiency resulted in impaired emigration of skin DCs to the lymph node and contact hypersensitivity was dramatically reduced in the absence of mast cells. In addition, mast cell-specific inactivation of the Il10 gene did not reveal any role for mast cell-derived IL-10 in the regulation of contact allergy. Collectively, we demonstrate that mast cells are essential promoters of contact hypersensitivity, thereby highlighting their potential to promote immune responses to antigens entering via the skin.
Publisher Cell Press
ISSN/ISBN 1074-7613 ; 1097-4180
edoc-URL https://edoc.unibas.ch/70810/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.immuni.2011.03.028
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/21703544
ISI-Number WOS:000292349700016
Document type (ISI) Journal Article
 
   

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