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首页> 外文期刊>Nature reviews. Gastroenterology & hepatology >IL-12, IL-23 and IL-17 in IBD: immunobiology and therapeutic targeting.
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IL-12, IL-23 and IL-17 in IBD: immunobiology and therapeutic targeting.

机译:IBD中IL-12,IL-23和IL-17:免疫生物学和治疗靶向。

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摘要

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.
机译:IL-12和IL-23是密切相关的细胞因子,在组织炎症调节中具有重要作用。 从小鼠,人类观察研究和人口遗传学中的研究融合证据支持这些细胞因子在肠道中粘膜炎症调节中的重要性。 Ustekinumab,靶向细胞因子的治疗性抗体现在广泛用于治疗克罗恩病,包括在欧洲,美国,加拿大和日本,同时靶向IL-23的代理商是晚期临床试验。 我们审查了对IL-12和IL-23生物学的新兴了解,以及其主要下游细胞因子,包括IL-17。 特别是,我们讨论了他们的生物学如何影响IBD的临床试验和治疗策略的发展,以及如何惊讶地发现临床试验的发现,依次重新分为我们对潜在生物学的理解。

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