直接 NLRP3 抑制剂治疗炎症性疾病的研究进展

IF 3.7 4区 医学 Q2 CELL BIOLOGY
Xiu Chen, Pingping Zhang, Yu Zhang, Mengzhu Wei, Tian Tian, Dacheng Zhu, Yanling Guan, Wei Wei, Yang Ma
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引用次数: 0

摘要

NLRP3 炎症小体是一种细胞质多蛋白复合物,具有识别多种病原体衍生因子、环境因子和内源性应激相关因子的能力。NLRP3 炎症小体的失调激活与各种炎症小体相关疾病的发生有关,这凸显了它作为治疗炎症性疾病关键靶点的重要性。然而,尽管NLRP3炎症小体具有重要的临床意义,但目前仍缺乏直接靶向NLRP3炎症小体的特效药物。针对 NLRP3 炎性体的不同方面,已经探索出多种策略,其中以直接抑制 NLRP3 为目的的干预措施显示出最有希望的疗效和安全性。在这篇综述中,我们总结了针对 NLRP3 的直接抑制剂,阐明了它们的抑制机制、临床试验阶段和潜在应用。通过讨论,我们希望阐明抑制 NLRP3 对治疗炎症性疾病的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The research progression of direct NLRP3 inhibitors to treat inflammatory disorders

The NLRP3 inflammasome represents a cytoplasmic multiprotein complex with the capability to recognize a wide range of pathogen-derived, environmental, and endogenous stress-related factors. Dysregulated activation of the NLRP3 inflammasome has been implicated in the development of various inflammasome-associated disorders, highlighting its significance as a pivotal target for the treatment of inflammatory diseases. Nonetheless, despite its clinical importance, there is currently a lack of specific drugs available for directly targeting the NLRP3 inflammasome. Several strategies have been explored to target different facets of the NLRP3 inflammasome, with interventions aimed at directly inhibiting NLRP3 demonstrating the most promising efficacy and safety profiles. In this review, we provide a summary of direct inhibitors targeting NLRP3, elucidating their inhibitory mechanisms, clinical trial phases, and potential applications. Through this discussion, we aim to shed light on the implications of NLRP3 inhibition for the treatment of inflammatory diseases.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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