Hengyang Medical School, Cancer Research Institute, University of South China, Chang Sheng Xi Avenue 28, Hengyang City, Hunan, 421001, People's Republic of China.
Inflamm Res. 2023 Nov;72(10-11):2023-2036. doi: 10.1007/s00011-023-01801-4. Epub 2023 Oct 9.
Myeloid differentiation factor-88 (MyD88) is a crucial adapter protein that coordinates the innate immune response and establishes an adaptive immune response. The interaction of the Toll/Interleukin-1 receptor (IL-1R) superfamily with MyD88 triggers the activation of various signalling pathways such as nuclear factor-κB (NF-κB) and activator protein-1 (AP-1), promoting the production of a variety of immune and inflammatory mediators and potentially driving the development of a variety of diseases.
This article will explore the therapeutic potential and mechanism of the MyD88-specific inhibitor ST2825 and describe its use in the treatment of several diseases. We envision future research and clinical applications of ST2825 to provide new ideas for the development of anti-inflammatory drugs and disease-specific drugs to open new horizons for the prevention and treatment of related inflammatory diseases.
This review analysed relevant literature in PubMed and other databases. All relevant studies on MyD88 inhibitors and ST2825 that were published in the last 20 years were used as screening criteria. These studies looked at the development and improvement of MyD88 inhibitors and ST2825.
Recent evidence using the small-molecule inhibitor of ST2825 has suggested that blocking MyD88 activity can be used to treat diseases such as neuroinflammation, inflammatory diseases such as acute liver/kidney injury, or autoimmune diseases such as systemic lupus erythematosus and can affect transplantation immunity. In addition, ST2825 has potential therapeutic value in B-cell lymphoma with the MyD88 L265P mutation.
Targeting MyD88 is a novel therapeutic strategy, and scientific research is presently focused on the development of MyD88 inhibitors. The peptidomimetic compound ST2825 is a widely studied small-molecule inhibitor of MyD88. Thus, ST2825 may be a potential therapeutic small-molecule agent for modulating host immune regulation in inflammatory diseases and inflammatory therapy.
髓样分化因子 88(MyD88)是一种关键的衔接蛋白,协调先天免疫反应并建立适应性免疫反应。Toll/白细胞介素-1 受体(IL-1R)超家族与 MyD88 的相互作用触发各种信号通路的激活,如核因子-κB(NF-κB)和激活蛋白-1(AP-1),促进各种免疫和炎症介质的产生,并可能驱动多种疾病的发展。
本文将探讨 MyD88 特异性抑制剂 ST2825 的治疗潜力和机制,并描述其在几种疾病治疗中的应用。我们设想未来对 ST2825 的研究和临床应用将为抗炎药物和疾病特异性药物的开发提供新的思路,为相关炎症性疾病的防治开辟新的前景。
本综述分析了 PubMed 及其他数据库中的相关文献。将过去 20 年发表的关于 MyD88 抑制剂和 ST2825 的所有相关研究作为筛选标准,这些研究着眼于 MyD88 抑制剂和 ST2825 的开发和改进。
最近使用小分子抑制剂 ST2825 的证据表明,阻断 MyD88 活性可用于治疗神经炎症、急性肝/肾损伤等炎症性疾病或系统性红斑狼疮等自身免疫性疾病,并可能影响移植免疫。此外,ST2825 对携带 MyD88 L265P 突变的 B 细胞淋巴瘤具有潜在的治疗价值。
靶向 MyD88 是一种新的治疗策略,目前的科学研究集中在开发 MyD88 抑制剂上。肽模拟化合物 ST2825 是一种广泛研究的 MyD88 小分子抑制剂。因此,ST2825 可能是一种有潜力的调节宿主免疫调节的治疗性小分子药物,可用于炎症性疾病和炎症治疗。