Small molecule allosteric inhibitors of RORγt block Th17-dependent inflammation and associated gene expression in vivo.
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ABSTRACT: Retinoic acid receptor-related orphan nuclear receptor (ROR) γt is a member of the RORC nuclear hormone receptor family of transcription factors. RORγt functions as a critical regulator of thymopoiesis and immune responses. RORγt is expressed in multiple immune cell populations including Th17 cells, where its primary function is regulation of immune responses to bacteria and fungi through IL-17A production. However, excessive IL-17A production has been linked to numerous autoimmune diseases. Moreover, Th17 cells have been shown to elicit both pro- and anti-tumor effects. Thus, modulation of the RORγt/IL-17A axis may represent an attractive therapeutic target for the treatment of autoimmune disorders and some cancers. Herein we report the design, synthesis and characterization of three sele
SUBMITTER: Saenz SA
PROVIDER: S-EPMC8577775 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
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