C/EBP? Promotes Immunity to Oral Candidiasis through Regulation of ?-Defensins.

ABSTRACT: Humans or mice subjected to immunosuppression, such as corticosteroids or anti-cytokine biologic therapies, are susceptible to mucosal infections by the commensal fungus Candida albicans. Recently it has become evident that the Th17/IL-17 axis is essential for immunity to candidiasis, but the downstream events that control immunity to this fungus are poorly understood. The CCAAT/Enhancer Binding Protein-? (C/EBP?) transcription factor is important for signaling by multiple inflammatory stimuli, including IL-17. C/EBP? is regulated in a variety of ways by IL-17, and controls several downstream IL-17 target genes. However, the role of C/EBP? in vivo is poorly understood, in part because C/EBP?-deficient mice are challenging to breed and work with. In this study, we sought to understand the role of C/EBP? in the context of an IL-17-dependent immune response, using C. albicans infection as a model system. Confirming prior findings, we found that C/EBP? is required for immunity to systemic candidiasis. In contrast, C/EBP?(-/-) mice were resistant to oropharyngeal candidiasis (OPC), in a manner indistinguishable from immunocompetent WT mice. However, C/EBP?(-/-) mice experienced more severe OPC than WT mice in the context of cortisone-induced immunosuppression. Expression of the antimicrobial peptide ?-defensin (BD)-3 correlated strongly with susceptibility in C/EBP?(-/-) mice, but no other IL-17-dependent genes were associated with susceptibility. Therefore, C/EBP? contributes to immunity to mucosal candidiasis during cortisone immunosuppression in a manner linked to ?-defensin 3 expression, but is apparently dispensable for the IL-17-dependent response.

SUBMITTER: Simpson-Abelson MR 

PROVIDER: S-EPMC4552893 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature