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Selective C-Rel Activation via Malt1 Controls Anti-Fungal T-H-17 Immunity by Dectin-1 and Dectin-2

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

C-type lectins dectin-1 and dectin-2 on dendritic cells elicit protective immunity against fungal infections through induction of T(H)1 and T-H-17 cellular responses. Fungal recognition by dectin-1 on human dendritic cells engages the CARD9-Bcl10-Malt1 module to activate NF-kappa B. Here we demonstrate that Malt1 recruitment is pivotal to T-H-17 immunity by selective activation of NF-kappa B subunit c-Rel, which induces expression of T-H-17-polarizing cytokines IL-1 beta and IL-23p19. Malt1 inhibition abrogates c-Rel activation and T-H-17 immunity to Candida species. We found that Malt1-mediated activation of c-Rel is similarly essential to induction of T-H-17-polarizing cytokines by dectin-2. Whereas dectin-1 activates all NF-kappa B subunits, dectin-2 selectively activates c-Rel, signifying a specialized T-H-17-enhancing function for dectin-2 in anti-fungal immunity by human dendritic cells. Thus, dectin-1 and dectin-2 control adaptive T-H-17 immunity to fungi via Malt1-dependent activation of c-Rel
Original languageEnglish
Pages (from-to)e1001259
JournalPLoS pathogens
Volume7
Issue number1
DOIs
Publication statusPublished - 2011

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