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抗集落刺激因子疗法治疗炎症和自身免疫性疾病。

Anti-colony-stimulating factor therapies for inflammatory and autoimmune diseases.

机构信息

University of Melbourne, Department of Medicine at The Royal Melbourne Hospital, Parkville, Victoria 3050, Australia.

GlaxoSmithKline, Medicines Research Centre, Stevenage SG1 2NY, UK.

出版信息

Nat Rev Drug Discov. 2016 Dec 29;16(1):53-70. doi: 10.1038/nrd.2016.231.

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF), macrophage colony-stimulating factor (M-CSF; also known as CSF1), granulocyte colony-stimulating factor (G-CSF) and interleukin-3 (IL-3) can each play a part in the host response to injury and infection, and there is burgeoning interest in targeting these CSFs in inflammatory and autoimmune disorders, as well as in cancer. For success in clinical medicine, therapeutic targeting will need to be delineated from current strategies. The individual CSFs have unique biological roles, suggesting that they could be used to target specific conditions. This Review compares the CSFs, with a focus on how they could be targeted, discusses the relevant clinical trial data and summarizes the potential clinical applications of targeting each CSF. Importantly, we discuss the novelty of CSF biology and attempt to clarify some of the surrounding misconceptions and issues that can affect therapeutic decisions.

摘要

粒细胞-巨噬细胞集落刺激因子(GM-CSF)、巨噬细胞集落刺激因子(M-CSF;也称为 CSF1)、粒细胞集落刺激因子(G-CSF)和白细胞介素-3(IL-3)均可在宿主对损伤和感染的反应中发挥作用,并且人们对靶向这些 CSF 在炎症和自身免疫性疾病以及癌症中的作用越来越感兴趣。为了在临床医学中取得成功,需要从当前的策略中明确治疗靶向。单独的 CSF 具有独特的生物学作用,这表明它们可用于针对特定情况。这篇综述比较了 CSF,重点讨论了如何靶向它们,讨论了相关的临床试验数据,并总结了靶向每种 CSF 的潜在临床应用。重要的是,我们讨论了 CSF 生物学的新颖性,并试图阐明一些可能影响治疗决策的误解和问题。

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