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Cutting Edge: Nlrp10 Is Essential for Protective Antifungal Adaptive Immunity against Candida albicans
Author(s) -
Sophie Joly,
Stephanie C. Eisenbarth,
Alicia K. Olivier,
Adam Williams,
Daniel H. Kaplan,
Suzanne L. Cassel,
Richard A. Flavell,
Fayyaz S. Sutterwala
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1201715
Subject(s) - candida albicans , biology , immune system , corpus albicans , microbiology and biotechnology , immunity , immunology , acquired immune system , innate immune system , receptor , ex vivo , proinflammatory cytokine , cytokine , virulence , in vivo , inflammation , gene , genetics
Nucleotide-binding domain leucine-rich repeat containing receptors (NLRs) are cytosolic receptors that initiate immune responses to sterile and infectious insults to the host. Studies demonstrated that Nlrp3 is critical for the control of Candida albicans infections and in the generation of antifungal Th17 responses. In this article, we show that the NLR family member Nlrp10 also plays a unique role in the control of disseminated C. albicans infection in vivo. Nlrp10-deficient mice had increased susceptibility to disseminated candidiasis, as indicated by decreased survival and increased fungal burdens. In contrast to Nlrp3, Nlrp10 deficiency did not affect innate proinflammatory cytokine production from macrophages and dendritic cells challenged with C. albicans. However, Nlrp10-deficient mice displayed a profound defect in Candida-specific Th1 and Th17 responses. These results demonstrate a novel role for Nlrp10 in the generation of adaptive immune responses to fungal infection.

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