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• W2034453891 abstract "Chronic mucocutaneous candidiasis disease (CMCD) is characterized by recurrent or persistent infections of the skin, nails, and oral and genital mucosae caused by Candida albicans and, to a lesser extent, Staphylococcus aureus, in patients with no other infectious or autoimmune manifestations. We report two genetic etiologies of CMCD: autosomal recessive deficiency in the cytokine receptor, interleukin-17 receptor A (IL-17RA), and autosomal dominant deficiency of the cytokine interleukin-17F (IL-17F). IL-17RA deficiency is complete, abolishing cellular responses to IL-17A and IL-17F homo- and heterodimers. By contrast, IL-17F deficiency is partial, with mutant IL-17F-containing homo- and heterodimers displaying impaired, but not abolished, activity. These experiments of nature indicate that human IL-17A and IL-17F are essential for mucocutaneous immunity against C. albicans, but otherwise largely redundant." @default.
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• W2034453891 date "2011-04-01" @default.
• W2034453891 modified "2023-10-14" @default.
• W2034453891 title "Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity" @default.
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• W2034453891 doi "https://doi.org/10.1126/science.1200439" @default.
• W2034453891 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3070042" @default.
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