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从脂质到白细胞:动脉粥样硬化中的炎症与免疫细胞

Moving from lipids to leukocytes: inflammation and immune cells in atherosclerosis.

作者信息

Annink Maxim E, Kraaijenhof Jordan M, Stroes Erik S G, Kroon Jeffrey

机构信息

Department of Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.

Department of Experimental Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Cell Dev Biol. 2024 Aug 5;12:1446758. doi: 10.3389/fcell.2024.1446758. eCollection 2024.

DOI:10.3389/fcell.2024.1446758
PMID:39161593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11330886/
Abstract

Atherosclerotic cardiovascular disease (ASCVD) is the most important cause of morbidity and mortality worldwide. While it is traditionally attributed to lipid accumulation in the vascular endothelium, recent research has shown that plaque inflammation is an important additional driver of atherogenesis. Though clinical outcome trials utilizing anti-inflammatory agents have proven promising in terms of reducing ASCVD risk, it is imperative to identify novel actionable targets that are more specific to atherosclerosis to mitigate adverse effects associated with systemic immune suppression. To that end, this review explores the contributions of various immune cells from the innate and adaptive immune system in promoting and mitigating atherosclerosis by integrating findings from experimental studies, high-throughput multi-omics technologies, and epidemiological research.

摘要

动脉粥样硬化性心血管疾病(ASCVD)是全球发病和死亡的最重要原因。虽然传统上认为它是由于脂质在血管内皮中积累所致,但最近的研究表明,斑块炎症是动脉粥样硬化发生的另一个重要驱动因素。尽管使用抗炎药物的临床结局试验在降低ASCVD风险方面已显示出前景,但必须确定更针对动脉粥样硬化的新型可操作靶点,以减轻与全身免疫抑制相关的不良反应。为此,本综述通过整合实验研究、高通量多组学技术和流行病学研究的结果,探讨了先天免疫系统和适应性免疫系统中各种免疫细胞在促进和减轻动脉粥样硬化方面的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/35f5173dc97c/fcell-12-1446758-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/16d04dbc0275/fcell-12-1446758-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/cf03f921b9a4/fcell-12-1446758-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/35f5173dc97c/fcell-12-1446758-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/16d04dbc0275/fcell-12-1446758-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/cf03f921b9a4/fcell-12-1446758-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ee/11330886/35f5173dc97c/fcell-12-1446758-g003.jpg

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Organ-specific vasculature-on-a-chip systems.器官特异性芯片上血管系统。
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Single-cell T cell receptor sequencing of paired human atherosclerotic plaques and blood reveals autoimmune-like features of expanded effector T cells.
严重发热伴血小板减少综合征患者的血脂异常:一项回顾性队列研究。
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对配对的人类动脉粥样硬化斑块和血液进行单细胞T细胞受体测序,揭示了扩增的效应T细胞的自身免疫样特征。
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Marginal zone B cells produce 'natural' atheroprotective IgM antibodies in a T cell-dependent manner.边缘区 B 细胞在 T 细胞依赖性方式下产生“天然”的抗动脉粥样硬化 IgM 抗体。
Cardiovasc Res. 2024 Mar 14;120(3):318-328. doi: 10.1093/cvr/cvae027.
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Regulatory T-Cell Response to Low-Dose Interleukin-2 in Ischemic Heart Disease.调节性 T 细胞对缺血性心脏病中低剂量白细胞介素-2 的反应。
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