抗动脉粥样硬化机制和治疗。

IF 5.2 2区 医学 Q1 PERIPHERAL VASCULAR DISEASE
Alex Hudson, Oluwakemi O Igiehon, Matthew D Woolard, Arif Yurdagul
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引用次数: 0

摘要

综述目的:本综述探讨了抗动脉粥样硬化机制和efferocytosis在促进炎症消退中的关键作用,重点介绍了旨在恢复血管稳态和减缓动脉粥样硬化进展的创新的、基于消退的治疗策略。最近发现:动脉粥样硬化是一种慢性炎症,可因efferocytosis受损而加剧,这有助于斑块不稳定和坏死核心的扩张。先进的分子和细胞分析揭示了不同的巨噬细胞群体及其在efferocytosis过程中的代谢适应,这推动了组织修复所必需的溶解介质的产生。失调的信号和代谢途径破坏了凋亡细胞的有效清除,加剧了炎症。分子调节因子,如microrna,进一步影响胞饮,控制心血管结局。基于溶解的治疗,包括专门的促溶解介质、肽和代谢物,在维持宿主免疫功能的同时增强凋亡细胞的连续清除,比传统的免疫抑制方法具有优势。此外,针对疾病特异性抗原的疫苗有望引发保护性免疫反应,有助于改善动脉粥样硬化。Efferocytosis是动脉粥样硬化炎症消退的关键调节因子,将巨噬细胞代谢与斑块稳定性联系起来。它的破坏驱动疾病进展,但新兴疗法针对解决途径,代谢重编程和免疫调节具有有效干预的潜力。分析技术和靶向给药系统的进步将解决转化方面的挑战,为精准医学治疗动脉粥样硬化性心血管疾病铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-Atherogenic Mechanisms and Therapies.

Anti-Atherogenic Mechanisms and Therapies.

Purpose of review: This review examines anti-atherogenic mechanisms and the crucial role of efferocytosis in promoting inflammation resolution, with a focus on innovative, resolution-based therapeutic strategies that aim to restore vascular homeostasis and mitigate atherosclerosis progression.

Recent findings: Atherosclerosis, a chronic inflammatory condition, is exacerbated by impaired efferocytosis, which contributes to plaque instability and the expansion of the necrotic core. Advanced molecular and cellular profiling has revealed diverse macrophage populations and their metabolic adaptations during efferocytosis, which drive the production of resolving mediators essential for tissue repair. Dysregulated signaling and metabolic pathways disrupt the efficient clearance of apoptotic cells, exacerbating inflammation. Molecular regulators, such as microRNAs, further impact efferocytosis, governing cardiovascular outcomes. Resolution-based therapies, including specialized pro-resolving mediators, peptides, and metabolites, enhance the successive clearance of apoptotic cells while maintaining host immune function, offering advantages over traditional immunosuppressive approaches. Additionally, vaccines targeting disease-specific antigens show promise in eliciting protective immune responses that can help ameliorate atherosclerosis. Efferocytosis is a key regulator of inflammation resolution in atherosclerosis, linking macrophage metabolism to plaque stability. Its disruption drives disease progression, but emerging therapies targeting resolution pathways, metabolic reprogramming, and immune modulation hold the potential for effective interventions. Advances in profiling technologies and targeted delivery systems will address translational challenges, paving the way for precision medicine in treating atherosclerotic cardiovascular disease.

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来源期刊
CiteScore
9.00
自引率
3.40%
发文量
87
审稿时长
6-12 weeks
期刊介绍: The aim of this journal is to systematically provide expert views on current basic science and clinical advances in the field of atherosclerosis and highlight the most important developments likely to transform the field of cardiovascular prevention, diagnosis, and treatment. We accomplish this aim by appointing major authorities to serve as Section Editors who select leading experts from around the world to provide definitive reviews on key topics and papers published in the past year. We also provide supplementary reviews and commentaries from well-known figures in the field. An Editorial Board of internationally diverse members suggests topics of special interest to their country/region and ensures that topics are current and include emerging research.
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