The Progress of Immune Cells-induced Inflammatory Response in Gout.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Jing Liu, Ge Liu, Teng Chu, Yue Wu, Lele Zixin Yang, Weirong Fang
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引用次数: 0

Abstract

Gout, based on hyperuricemia, is an immune disease characterized by redness and pain caused by monosodium urate (MSU) deposition in the joints. Inflammation is the fundamental cause of gout symptoms, and many immune cells, such as monocytes/macrophages, neutrophils, and T lymphocytes, have been shown to be involved in various processes of pathological progress. This study reviews the changes and functions of different immune cells during the occurrence and development of gout, focusing on the mechanisms and signaling pathways by which macrophages activate nod-like receptor pyrin-containing 3 (NLRP3) inflammasome to initiate gout inflammation in order to further elucidate the pathogenesis of gout and provide new targets for the research of anti-gout drugs.

痛风免疫细胞诱导炎症反应的研究进展。
痛风是一种基于高尿酸血症的免疫性疾病,其特征是由尿酸钠(MSU)沉积在关节中引起的红肿和疼痛。炎症是痛风症状的根本原因,许多免疫细胞,如单核/巨噬细胞、中性粒细胞和T淋巴细胞,已被证明参与了各种病理进展过程。本研究综述了痛风发生发展过程中不同免疫细胞的变化和功能,重点探讨了巨噬细胞激活nod-like receptor pyrin-containing 3 (NLRP3)炎性体引发痛风炎症的机制和信号通路,以期进一步阐明痛风的发病机制,为抗痛风药物的研究提供新的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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