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IL-12、IL-23 和 IL-17 在炎症性肠病中的作用:免疫生物学和治疗靶点。

IL-12, IL-23 and IL-17 in IBD: immunobiology and therapeutic targeting.

机构信息

Christian Doppler Laboratory for Mucosal Immunology, Medical University Innsbruck, Innsbruck, Austria.

Department of Medicine, Division of Internal Medicine 1, Medical University Innsbruck, Innsbruck, Austria.

出版信息

Nat Rev Gastroenterol Hepatol. 2019 Mar;16(3):185-196. doi: 10.1038/s41575-018-0084-8.

Abstract

IL-12 and IL-23 are closely related cytokines with important roles in the regulation of tissue inflammation. Converging evidence from studies in mice, human observational studies and population genetics supports the importance of these cytokines in the regulation of mucosal inflammation in the gut in particular. Ustekinumab, a therapeutic antibody targeting both cytokines is now widely licensed for the treatment of Crohn's disease, including in Europe, the USA, Canada and Japan, whilst agents targeting IL-23 specifically are in late-phase clinical trials. We review the emerging understanding of the biology of IL-12 and IL-23, as well as that of their major downstream cytokines, including IL-17. In particular, we discuss how their biology has influenced the development of clinical trials and therapeutic strategies in IBD, as well as how findings from clinical trials, at times surprising, have in turn refocused our understanding of the underlying biology.

摘要

IL-12 和 IL-23 是密切相关的细胞因子,在调节组织炎症方面具有重要作用。来自小鼠研究、人类观察性研究和群体遗传学的综合证据支持这些细胞因子在调节肠道黏膜炎症中的重要性。乌司奴单抗是一种针对这两种细胞因子的治疗性抗体,现已在包括欧洲、美国、加拿大和日本在内的地区广泛获得批准,用于治疗克罗恩病,而专门针对 IL-23 的药物则处于后期临床试验阶段。我们综述了对 IL-12 和 IL-23 及其主要下游细胞因子(包括 IL-17)生物学的新认识。特别是,我们讨论了它们的生物学如何影响 IBD 临床试验和治疗策略的发展,以及临床试验的结果如何出人意料地重新聚焦了我们对潜在生物学的理解。

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