The Immunomodulatory Effects of Statins on Macrophages

Alan Sheridan, C. Wheeler-Jones, M. Gage
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引用次数: 7

Abstract

Statins are 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors used worldwide to manage dyslipidaemia and thus limit the development of atherosclerotic disease and its complications. These atheroprotective drugs are now known to exert pleiotropic actions outside of their cholesterol-lowering activity, including altering immune cell function. Macrophages are phagocytic leukocytes that play critical functional roles in the pathogenesis of atherosclerosis and are directly targeted by statins. Early studies documented the anti-inflammatory effects of statins on macrophages, but emerging evidence suggests that these drugs can also enhance pro-inflammatory macrophage responses, creating an unresolved paradox. This review comprehensively examines the in vitro, in vivo, and clinical literature to document the statin-induced changes in macrophage polarization and immunomodulatory functions, explore the underlying mechanisms involved, and offer potential explanations for this paradox. A better understanding of the immunomodulatory actions of statins on macrophages should pave the way for the development of novel therapeutic approaches to manage atherosclerosis and other chronic diseases and conditions characterised by unresolved inflammation.
他汀类药物对巨噬细胞的免疫调节作用
他汀类药物是3-羟基-3-甲基戊二酰辅酶A (HMG-CoA)还原酶抑制剂,用于控制血脂异常,从而限制动脉粥样硬化疾病及其并发症的发展。目前已知,这些动脉粥样硬化保护药物除了降低胆固醇外,还具有多种作用,包括改变免疫细胞功能。巨噬细胞是一种吞噬性白细胞,在动脉粥样硬化的发病机制中起着关键的功能作用,是他汀类药物的直接靶点。早期的研究记录了他汀类药物对巨噬细胞的抗炎作用,但新出现的证据表明,这些药物也可以增强促炎巨噬细胞的反应,这产生了一个未解决的悖论。本文综合研究了他汀类药物诱导巨噬细胞极化和免疫调节功能改变的体外、体内和临床文献,探讨了其中的潜在机制,并对这一悖论提供了可能的解释。更好地了解他汀类药物对巨噬细胞的免疫调节作用,将为开发新的治疗方法铺平道路,以治疗动脉粥样硬化和其他以未解决的炎症为特征的慢性疾病和病症。
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
Immuno-Analyse & Biologie Specialisee
Immuno-Analyse & Biologie Specialisee 医学-医学实验技术
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审稿时长
6-12 weeks
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