Cohen Shira, Fishman Pnina
Can-Fite BioPharma Ltd., Kiryat-Matalon, Petah-Tikva 49170, Israel,
Drug Des Devel Ther. 2019 Jan 30;13:491-497. doi: 10.2147/DDDT.S195294. eCollection 2019.
Cancer patients undergoing immunotherapy may develop cytokine release syndrome (CRS), an inflammatory cytokine storm condition, followed by neurotoxic manifestations and may be life-threatening. The current treatments for CRS successfully reduce the inflammatory response but may limit the anticancer effect of the given immunotherapy and fail to overcome the neurotoxic adverse events. Adenosine, a ubiquitous purine nucleoside, induces a plethora of effects in the body via its binding to four adenosine receptors A, A, A, and the A. Highly selective agonists to the A adenosine receptor act as inhibitors of proinflammatory cytokines, possess robust anti-inflammatory and anticancer activity, and concomitantly, induce neuroprotective effects. Piclidenoson and namodenoson belong to this group of compounds, are effective upon oral administration, show an excellent safety profile in human clinical studies, and therefore, may be considered as drug candidates to treat CRS. In this article, the detailed anti-inflammatory characteristics of these compounds and the rationale to use them as drugs to combat CRS are described.
接受免疫治疗的癌症患者可能会发生细胞因子释放综合征(CRS),这是一种炎症性细胞因子风暴状态,随后会出现神经毒性表现,且可能危及生命。目前针对CRS的治疗方法虽能成功减轻炎症反应,但可能会限制所给予免疫治疗的抗癌效果,且无法克服神经毒性不良事件。腺苷是一种普遍存在的嘌呤核苷,它通过与四种腺苷受体A1、A2A、A2B和A3结合在体内引发多种效应。A2A腺苷受体的高选择性激动剂可作为促炎细胞因子的抑制剂,具有强大的抗炎和抗癌活性,同时还能诱导神经保护作用。匹立地诺松和纳莫地诺松属于这类化合物,口服有效,在人体临床研究中显示出优异的安全性,因此可被视为治疗CRS的候选药物。本文描述了这些化合物详细的抗炎特性以及将它们用作对抗CRS药物的基本原理。