Suppr超能文献

RRx-001 综述:一种晚期多适应症 NLRP3 激活和慢性炎症抑制剂。

A Review of RRx-001: A Late-Stage Multi-Indication Inhibitor of NLRP3 Activation and Chronic Inflammation.

机构信息

Faculty of Medicine, UQ Centre for Clinical Research (UQCCR), The University of Queensland, Brisbane, 4029, Australia.

EpicentRx, Torrey Pines, CA, 92307, USA.

出版信息

Drugs. 2023 Apr;83(5):389-402. doi: 10.1007/s40265-023-01838-z. Epub 2023 Mar 15.

Abstract

Chronic unresolving inflammation is emerging as a key underlying pathological feature of many if not most diseases ranging from autoimmune conditions to cardiometabolic and neurological disorders. Dysregulated immune and inflammasome activation is thought to be the central driver of unresolving inflammation, which in some ways provides a unified theory of disease pathology and progression. Inflammasomes are a group of large cytosolic protein complexes that, in response to infection- or stress-associated stimuli, oligomerize and assemble to generate a platform for driving inflammation. This occurs through proteolytic activation of caspase-1-mediated inflammatory responses, including cleavage and secretion of the proinflammatory cytokines interleukin (IL)-1β and IL-18, and initiation of pyroptosis, an inflammatory form of cell death. Several inflammasomes have been characterized. The most well-studied is the nucleotide-binding domain (NOD)-like receptor protein 3 (NLRP3) inflammasome, so named because the NLRP3 protein in the complex, which is primarily present in immune and inflammatory cells following activation by inflammatory stimuli, belongs to the family of nucleotide-binding and oligomerization domain (Nod) receptor proteins. Several NLRP3 inflammasome inhibitors are in development, all with multi-indication activity. This review discusses the current status, known mechanisms of action, and disease-modifying therapeutic potential of RRx-001, a direct NLRP3 inflammasome inhibitor under investigation in several late-stage anticancer clinical trials, including a phase 3 trial for the treatment of third-line and beyond small cell lung cancer (SCLC), an indication with no treatment, in which RRx-001 is combined with reintroduced chemotherapy from the first line, carboplatin/cisplatin and etoposide (ClinicalTrials.gov Identifier: NCT03699956). Studies from multiple independent groups have now confirmed that RRx-001 is safe and well tolerated in humans. Additionally, emerging evidence in preclinical animal models suggests that RRx-001 could be effective in a wide range of diseases where immune and inflammasome activation drives disease pathology.

摘要

慢性未解决的炎症正在成为许多疾病(如果不是大多数疾病的话)的关键潜在病理特征,这些疾病范围从自身免疫性疾病到心血管代谢和神经紊乱。免疫失调和炎症小体激活被认为是未解决炎症的核心驱动因素,在某种程度上为疾病的病理和进展提供了一个统一的理论。炎症小体是一组大型胞质蛋白复合物,在响应感染或应激相关刺激时,寡聚化并组装以产生驱动炎症的平台。这是通过半胱天冬酶-1 介导的炎症反应的蛋白水解激活来实现的,包括促炎细胞因子白细胞介素 (IL)-1β 和 IL-18 的切割和分泌,以及起始细胞焦亡,这是一种炎症形式的细胞死亡。已经描述了几种炎症小体。研究最充分的是核苷酸结合域 (NOD)-样受体蛋白 3 (NLRP3) 炎症小体,之所以这样命名,是因为该复合物中的 NLRP3 蛋白在被炎症刺激激活后主要存在于免疫和炎症细胞中,属于核苷酸结合和寡聚化域 (Nod) 受体蛋白家族。几种 NLRP3 炎症小体抑制剂正在开发中,所有这些抑制剂都具有多适应症活性。本文讨论了 RRx-001 的现状、已知的作用机制以及在几种晚期抗癌临床试验中的疾病修饰治疗潜力,包括用于治疗三线及以上小细胞肺癌 (SCLC) 的 3 期临床试验,这是一种没有治疗方法的适应症,其中 RRx-001 与重新引入一线化疗相结合,包括卡铂/顺铂和依托泊苷(临床试验标识符:NCT03699956)。来自多个独立小组的研究现在已经证实,RRx-001 在人类中是安全且耐受良好的。此外,在临床前动物模型中出现的新证据表明,RRx-001 在广泛的疾病中可能有效,其中免疫和炎症小体激活驱动疾病病理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc84/10042757/8bac96e89ca5/40265_2023_1838_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验