芳香烃受体
伊米奎莫德
银屑病
细胞因子
人体皮肤
兴奋剂
促炎细胞因子
免疫学
医学
炎症
离体
受体
体内
癌症研究
生物
内科学
转录因子
生物化学
遗传学
生物技术
基因
作者
Susan Smith,Channa Jayawickreme,David J. Rickard,Edwige Nicodème,Thi Tho Bui,Cathy Simmons,Christine M. Coquery,Jessica Neil,William M. Pryor,David Mayhew,Deepak K. Rajpal,Katrina L. Creech,Sylvia M. Furst,James Lee,Dalei Wu,Fraydoon Rastinejad,Timothy M. Willson,Fabrice Viviani,David C. Morris,John T. Moore,Javier Cote-Sierra
标识
DOI:10.1016/j.jid.2017.05.004
摘要
Tapinarof (GSK2894512) is a naturally derived topical treatment with demonstrated efficacy for patients with psoriasis and atopic dermatitis, although the biologic target and mechanism of action had been unknown. We demonstrate that the anti-inflammatory properties of tapinarof are mediated through activation of the aryl hydrocarbon receptor (AhR). We show that tapinarof binds and activates AhR in multiple cell types, including cells of the target tissue-human skin. In addition, tapinarof moderates proinflammatory cytokine expression in stimulated peripheral blood CD4+ T cells and ex vivo human skin, and impacts barrier gene expression in primary human keratinocytes; both of these processes are likely to be downstream of AhR activation based on current evidence. That the anti-inflammatory properties of tapinarof derive from AhR agonism is conclusively demonstrated using the mouse model of imiquimod-induced psoriasiform skin lesions. Topical treatment of AhR-sufficient mice with tapinarof leads to compound-driven reductions in erythema, epidermal thickening, and tissue cytokine levels. In contrast, tapinarof has no impact on imiquimod-induced skin inflammation in AhR-deficient mice. In summary, these studies identify tapinarof as an AhR agonist and confirm that its efficacy is dependent on AhR.
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