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Retroviral CRISPR/Cas9-Mediated Gene Targeting for the Study of Th17 Differentiation in Vitro
Published on: November 15, 2024
Targeting the IL-17A Cytokine Interface: Structural Insights and Small-Molecule Modulators
Gyeong Un Kim1,2, Ansoo Lee1,2, Sanghee Lee1,3
1Medicinal Materials Research Center, Biomedical Division, Korea Institute of Science and Technology, Seoul02792, Republic of Korea.
Abstract:
Interleukin-17A (IL-17A) is a proinflammatory cytokine that occupies a central position at the interface of host defense, tissue homeostasis, and chronic inflammation. While IL-17A plays essential roles in antimicrobial immunity and epithelial barrier integrity, dysregulated IL-17A signaling drives the pathogenesis of autoimmune and inflammatory diseases. This functional duality underlies both the clinical success and the inherent limitations of IL-17A signaling-neutralizing therapies, highlighting the need for selective and context-dependent modulation. In this perspective, we provide an overview of IL-17A signaling, from cytokine production to receptor-proximal signal transduction and therapeutic intervention. We then discuss small-molecule IL-17A antagonists identified through structure-guided approaches, with an emphasis on key binding modes, and briefly summarize compounds discovered through assay-based strategies. Beyond antagonism, we also examine the emerging concept of IL-17RA agonism, which remains largely unexplored. Collectively, this perspective highlights the importance of context-dependent small-molecule modulation of IL-17A signaling.
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