C-type lectin receptors differentially induce th17 cells and vaccine immunity to the endemic mycosis of North America

H Wang, V LeBert, CY Hung, K Galles… - The Journal of …, 2014 - journals.aai.org
H Wang, V LeBert, CY Hung, K Galles, S Saijo, X Lin, GT Cole, BS Klein, M Wüthrich
The Journal of Immunology, 2014journals.aai.org
Vaccine immunity to the endemic mycoses of North America requires Th17 cells, but the
pattern recognition receptors and signaling pathways that drive these protective responses
have not been defined. We show that C-type lectin receptors exert divergent contributions to
the development of antifungal Th17 cells and vaccine resistance against Blastomyces
dermatitidis, Histoplasma capsulatum, and Coccidioides posadasii. Acquired immunity to B.
dermatitidis requires Dectin-2, whereas vaccination against H. capsulatum and C. posadasii …
Abstract
Vaccine immunity to the endemic mycoses of North America requires Th17 cells, but the pattern recognition receptors and signaling pathways that drive these protective responses have not been defined. We show that C-type lectin receptors exert divergent contributions to the development of antifungal Th17 cells and vaccine resistance against Blastomyces dermatitidis, Histoplasma capsulatum, and Coccidioides posadasii. Acquired immunity to B. dermatitidis requires Dectin-2, whereas vaccination against H. capsulatum and C. posadasii infection depends on innate sensing by Dectin-1 and Dectin-2, but not Mincle. Tracking Ag-specific T cells in vivo established that the Card9 signaling pathway acts indispensably and exclusively on differentiation of Th17 cells, while leaving intact their activation, proliferation, survival, and migration. Whereas Card9 signaling is essential, C-type lectin receptors offer distinct and divergent contributions to vaccine immunity against these endemic fungal pathogens. Our work provides new insight into innate immune mechanisms that drive vaccine immunity and Th17 cells.
journals.aai.org