Langerhans cells suppress contact hypersensitivity responses via cognate CD4 interaction and langerhans cell-derived IL-10

Botond Z. Igyarto, Matthew C. Jenison, Jan C. Dudda, Axel Roers, Werner Müller, Pandelakis A. Koni, Daniel J. Campbell, Mark J. Shlomchik, Daniel H. Kaplan

Research output: Contribution to journalArticlepeer-review

109 Scopus citations

Abstract

Mice lacking epidermal Langerhans cells (LC) develop exaggerated contact-hypersensitivity (CHS) responses due to the absence of LC during sensitization/initiation. Examination of T cell responses reveals that the absence of LC leads to increased numbers of hapten-specific CD4 and CD8 T cells but does not alter cytokine expression or development of T regulatory cells. CHS responses and Ag-specific T cells are increased in mice in which MHC class II is ablated specifically in LC suggesting that direct cognate interaction between LC and CD4 cells is required for suppression. LC-derived IL-10 is also required for optimal inhibition of CHS. Both LC-derived IL-10-mediated suppression and full LC activation require LC expression of MHC class II. These data support a model in which cognate interaction of LC with CD4 T cells enables LC to inhibit expansion of Ag-specific responses via elaboration of IL-10.

Original languageEnglish (US)
Pages (from-to)5085-5093
Number of pages9
JournalJournal of Immunology
Volume183
Issue number8
DOIs
StatePublished - Oct 15 2009

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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