阿纳基纳
半胱氨酸蛋白酶1
拟肽
卡那努马布
药理学
化学
半胱氨酸蛋白酶
小分子
调解人
药物发现
炎症
医学
疾病
免疫学
细胞凋亡
肽
生物化学
炎症体
内科学
程序性细胞死亡
作者
Palmi Modi,Bhumi Shah,Shivani Patel
标识
DOI:10.1016/j.ejmech.2023.115861
摘要
Caspase-1 is a critical mediator of the inflammatory process by activating various pro-inflammatory cytokines such as pro-IL-1β, IL-18 and IL-33. Uncontrolled activation of caspase-1 leads to various cytokines-mediated diseases. Thus, inhibition of Caspase-1 is considered therapeutically beneficial to halt the progression of such diseases. Currently, rilonacept, canakinumab and anakinra are in use for caspase-1-mediated autoinflammatory diseases. However, the poor pharmacokinetic profile of these peptides limits their use as therapeutic agents. Therefore, several peptidomimetic inhibitors have been developed, but only a few compounds (VX-740, VX-765) have advanced to clinical trials; because of their toxic profile. Several small molecule inhibitors have also been progressing based on the three-dimensional structure of caspase-1. However there is no successful candidate available clinically. In this perspective, we highlight the mechanism of caspase-1 activation, its therapeutic potential as a disease target and potential therapeutic strategies targeting caspase-1 with their limitations.
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