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靶向 NLRP3 炎性小体的策略:临床前和临床研究。

Strategies for Targeting the NLRP3 Inflammasome in the Clinical and Preclinical Space.

机构信息

Chemical Biology, Merck & Co., Inc., 33 Avenue Louis Pasteur, Boston, Massachusetts 02115, United States.

出版信息

J Med Chem. 2021 Jan 14;64(1):101-122. doi: 10.1021/acs.jmedchem.0c01307. Epub 2020 Dec 22.

Abstract

Inhibiting the NLRP3 inflammasome mediates inflammation in an extensive number of preclinical models. As excitement in this field has grown, several companies have recently initiated testing of direct NLRP3 inhibitors in the clinic. At the same time, the NLRP3 inflammasome is part of a larger pro-inflammatory pathway, whose modulation is also being explored. Multiple targets in this pathway are already impinged upon by molecules that have been through clinical trials. These data, informed by the growing mechanistic understanding of the NLRP3 inflammasome in the preclinical space, provide a rich backdrop to assess the current state of the field. Here we explore attempts to inhibit the NLRP3 inflammasome in light of clinical and preclinical data around efficacy and safety.

摘要

抑制 NLRP3 炎性小体可在大量临床前模型中调节炎症。随着该领域的研究不断深入,一些公司最近已开始在临床中测试直接 NLRP3 抑制剂。与此同时,NLRP3 炎性小体是促炎途径的一部分,该途径的调节也在探索中。该途径中的多个靶点已经受到已通过临床试验的分子的影响。这些基于临床前空间中 NLRP3 炎性小体不断增长的机制理解的数据,为评估该领域的现状提供了丰富的背景。在此,我们根据临床和临床前数据,探讨了抑制 NLRP3 炎性小体在疗效和安全性方面的尝试。

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