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用于治疗炎症性疾病的白细胞介素-1受体相关激酶4(IRAK4)降解剂:进展与展望

Interleukin-1 Receptor-Associated Kinase 4 (IRAK4) Degraders for Treating Inflammatory Diseases: Advances and Prospects.

作者信息

Lin Yaoxiang, Zheng Lulu, Xu Ying, Wang Xinyan, Li Jie, Zheng Lei, Liang Guang, Chen Lingfeng

机构信息

School of Pharmacy, Hangzhou Medical College, Hangzhou 310014, China.

School of Medicine, Hangzhou Normal University, Hangzhou 311121, China.

出版信息

J Med Chem. 2025 Jan 23;68(2):902-914. doi: 10.1021/acs.jmedchem.4c01322. Epub 2025 Jan 6.

Abstract

Interleukin-1 receptor-associated kinase 4 (IRAK4) is involved in various inflammation-related diseases. Both the kinase and scaffolding functions of IRAK4 initiate pro-inflammatory factor transcription and expression. The scaffolding function of IRAK4 is essential for Myddosome assembly and NF-κB activation. Conventional small-molecule inhibitors effectively inhibit the kinase function of IRAK4 but do not block its scaffolding function. Recently, various IRAK4 degraders have shown promising therapeutic potential in inflammatory diseases. The most advanced IRAK4-selective degrader, KT-474 (SAR444656), significantly reduced inflammatory biomarker levels in patients and demonstrated high safety and tolerability. This perspective introduces and discusses the physiological biology of IRAK4, its associated diseases, and the current development of IRAK4 degraders, thereby offering insights into future research directions.

摘要

白细胞介素-1受体相关激酶4(IRAK4)参与多种炎症相关疾病。IRAK4的激酶和支架功能均可启动促炎因子的转录和表达。IRAK4的支架功能对于髓样分化因子88(MyD88)体的组装和核因子κB(NF-κB)的激活至关重要。传统的小分子抑制剂可有效抑制IRAK4的激酶功能,但不能阻断其支架功能。最近,各种IRAK4降解剂在炎症性疾病中显示出了有前景的治疗潜力。最先进的IRAK4选择性降解剂KT-474(SAR444656)显著降低了患者体内炎症生物标志物的水平,并显示出高安全性和耐受性。本文综述并讨论了IRAK4的生理生物学特性、其相关疾病以及IRAK4降解剂的当前研究进展,从而为未来的研究方向提供见解。

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