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ETS2在巨噬细胞炎症中的作用。

The Role of ETS2 in Macrophage Inflammation.

作者信息

Stankey Christina T, Lee James Christopher

机构信息

Genetic Mechanisms of Disease Lab, The Francis Crick Institute, London, United Kingdom.

Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.

出版信息

DNA Cell Biol. 2025 Jul;44(7):339-344. doi: 10.1089/dna.2025.0064. Epub 2025 Apr 14.

Abstract

Autoimmune and inflammatory diseases are rising globally yet widely effective therapies remain elusive. Most treatments have limited efficacy, significant potential side effects, or eventually lose response, underscoring the urgent need for new therapeutic approaches. We recently discovered that ETS2, a transcription factor, functions as a master regulator of macrophage-driven inflammation-and is causally linked to the pathogenesis of multiple inflammatory diseases via human genetics. The pleotropic inflammatory effects of ETS2 included upregulation of many cytokines that are individually targeted by current disease therapies, including TNFα, IL-23, IL1β, and TNF-like ligand 1A signaling. With the move toward combination treatment-to maximize efficacy-targeting ETS2 presents a unique opportunity to potentially induce a broad therapeutic effect. However, there will be multiple challenges to overcome since direct ETS2 inhibition is unlikely to be feasible. Here, we discuss these challenges and other unanswered questions about the central role that ETS2 plays in macrophage inflammation.

摘要

自身免疫性疾病和炎症性疾病在全球范围内呈上升趋势,但广泛有效的治疗方法仍然难以捉摸。大多数治疗方法疗效有限、存在显著的潜在副作用,或最终失去疗效,这凸显了对新治疗方法的迫切需求。我们最近发现,转录因子ETS2作为巨噬细胞驱动炎症的主要调节因子,通过人类遗传学与多种炎症性疾病的发病机制存在因果关系。ETS2的多效性炎症作用包括上调许多目前疾病治疗中单独靶向的细胞因子,包括肿瘤坏死因子α(TNFα)、白细胞介素23(IL-23)、白细胞介素1β(IL1β)和肿瘤坏死因子样配体1A信号传导。随着向联合治疗的转变(以最大化疗效),靶向ETS2提供了一个独特的机会,有可能诱导广泛的治疗效果。然而,由于直接抑制ETS2不太可能可行,因此将有多个挑战需要克服。在这里,我们讨论这些挑战以及关于ETS2在巨噬细胞炎症中所起核心作用的其他未解决问题。

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