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纳米免疫疗法治疗缺血性心脏病。

Nanoimmunotherapy to treat ischaemic heart disease.

机构信息

Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, location Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.

Department of Internal Medicine, Section of Nephrology, Amsterdam University Medical Centers, location Academic Medical Cente, University of Amsterdam, Amsterdam, Netherlands.

出版信息

Nat Rev Cardiol. 2019 Jan;16(1):21-32. doi: 10.1038/s41569-018-0073-1.

DOI:10.1038/s41569-018-0073-1
PMID:30209355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10621601/
Abstract

Atherosclerosis is a chronic disease of the large arteries and the underlying cause of myocardial infarction and stroke. Atherosclerosis is driven by cholesterol accumulation and subsequent inflammation in the vessel wall. Despite the clinical successes of lipid-lowering treatments, atherosclerosis remains one of the major threats to human health worldwide. Over the past 20 years, insights into cardiovascular immunopathology have provided a plethora of new potential therapeutic targets to reduce the risk of atherosclerosis and have shifted the therapeutic focus from lipids to inflammation. In 2017, the CANTOS trial demonstrated for the first time the beneficial effects of targeting inflammation to treat cardiovascular disease by showing that IL-1β inhibition can reduce the recurrence rate of cardiovascular events in a large cohort of patients. At the same time, preclinical studies have highlighted nanotechnology approaches that facilitate the specific targeting of innate immune cells, which could potentially generate more effective immunomodulatory treatments to induce disease regression and prevent the recurrence of cardiovascular events. The clinical translation of such nanoimmunotherapies and their application to treat patients with ischaemic heart disease are challenges that lie ahead.

摘要

动脉粥样硬化是一种大血管的慢性疾病,也是心肌梗死和中风的根本原因。动脉粥样硬化是由胆固醇在血管壁内的积累和随后的炎症所驱动的。尽管降脂治疗在临床上取得了成功,但动脉粥样硬化仍然是全世界人类健康的主要威胁之一。在过去的 20 年里,对心血管免疫病理学的深入了解为减少动脉粥样硬化的风险提供了大量新的潜在治疗靶点,并将治疗重点从脂质转移到炎症。2017 年,CANTOS 试验首次证明了通过靶向炎症来治疗心血管疾病的有益效果,表明 IL-1β 抑制可以降低一大群患者心血管事件的复发率。与此同时,临床前研究强调了纳米技术方法,这些方法可以促进固有免疫细胞的特异性靶向,这可能会产生更有效的免疫调节治疗方法,以诱导疾病消退并预防心血管事件的复发。这种纳米免疫疗法的临床转化及其在治疗缺血性心脏病患者中的应用是未来的挑战。

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Nanoimmunotherapy to treat ischaemic heart disease.纳米免疫疗法治疗缺血性心脏病。
Nat Rev Cardiol. 2019 Jan;16(1):21-32. doi: 10.1038/s41569-018-0073-1.
2
Targeting the immune response in atherosclerosis: It's time for clinical trials!针对动脉粥样硬化中的免疫反应:开展临床试验的时候到了!
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Exploring immune checkpoints as potential therapeutic targets in atherosclerosis.探讨免疫检查点作为动脉粥样硬化潜在治疗靶点的研究进展。
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Role of inflammation in the pathogenesis of atherosclerosis and therapeutic interventions.炎症在动脉粥样硬化发病机制中的作用及治疗干预。
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The Utility of Anti-Inflammatory Agents in Cardiovascular Disease: A Novel Perspective on the Treatment of Atherosclerosis.抗炎药物在心血管疾病中的应用:动脉粥样硬化治疗的新视角
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Novel anti-inflammatory therapies for the treatment of atherosclerosis.新型抗炎疗法治疗动脉粥样硬化。
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Interplay between hypercholesterolaemia and inflammation in atherosclerosis: Translating experimental targets into clinical practice.高脂血症与动脉粥样硬化中的炎症相互作用:将实验靶点转化为临床实践。
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1
Efficacy and safety assessment of a TRAF6-targeted nanoimmunotherapy in atherosclerotic mice and non-human primates.靶向TRAF6的纳米免疫疗法在动脉粥样硬化小鼠和非人灵长类动物中的疗效和安全性评估。
Nat Biomed Eng. 2018 May;2(5):279-292. doi: 10.1038/s41551-018-0221-2. Epub 2018 Apr 16.
2
Targeting CD40-Induced TRAF6 Signaling in Macrophages Reduces Atherosclerosis.靶向巨噬细胞中 CD40 诱导的 TRAF6 信号转导可减少动脉粥样硬化。
J Am Coll Cardiol. 2018 Feb 6;71(5):527-542. doi: 10.1016/j.jacc.2017.11.055.
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Resident and Monocyte-Derived Macrophages in Cardiovascular Disease.
基于纳米医学的静脉移植物疾病治疗策略。
Nat Rev Cardiol. 2025 Apr;22(4):255-272. doi: 10.1038/s41569-024-01094-y. Epub 2024 Nov 5.
4
Spatiotemporal control of neutrophil fate to tune inflammation and repair for myocardial infarction therapy.调控中性粒细胞命运以调控炎症和修复治疗心肌梗死。
Nat Commun. 2024 Oct 1;15(1):8481. doi: 10.1038/s41467-024-52812-6.
5
Resolvin D1 delivery to lesional macrophages using antioxidative black phosphorus nanosheets for atherosclerosis treatment.使用抗氧化黑磷纳米片将 resolvin D1 递送至病变巨噬细胞,用于动脉粥样硬化治疗。
Nat Nanotechnol. 2024 Sep;19(9):1386-1398. doi: 10.1038/s41565-024-01687-1. Epub 2024 Jun 19.
6
High-density lipoprotein mimetic nano-therapeutics targeting monocytes and macrophages for improved cardiovascular care: a comprehensive review.靶向单核细胞和巨噬细胞的高密度脂蛋白模拟纳米治疗药物改善心血管护理:全面综述。
J Nanobiotechnology. 2024 May 17;22(1):263. doi: 10.1186/s12951-024-02529-x.
7
Targeting macrophages with multifunctional nanoparticles to detect and prevent atherosclerotic cardiovascular disease.利用多功能纳米颗粒靶向巨噬细胞检测和预防动脉粥样硬化性心血管疾病。
Cardiovasc Res. 2024 Jul 2;120(8):819-838. doi: 10.1093/cvr/cvae099.
8
Biomimetic nanomedicines for precise atherosclerosis theranostics.用于精准动脉粥样硬化诊疗的仿生纳米药物
Acta Pharm Sin B. 2023 Nov;13(11):4442-4460. doi: 10.1016/j.apsb.2022.11.014. Epub 2022 Nov 15.
9
Effective Attenuation of Arteriosclerosis Following Lymphatic-Targeted Delivery of Hyaluronic Acid-Decorated Rapamycin Liposomes.基于透明质酸修饰的雷帕霉素脂质体淋巴靶向递释抑制动脉粥样硬化的作用
Int J Nanomedicine. 2023 Aug 2;18:4403-4419. doi: 10.2147/IJN.S410653. eCollection 2023.
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Therapeutic angiogenesis and tissue revascularization in ischemic vascular disease.缺血性血管疾病中的治疗性血管生成与组织再血管化
J Biol Eng. 2023 Feb 16;17(1):13. doi: 10.1186/s13036-023-00330-2.
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Circ Res. 2018 Jan 5;122(1):113-127. doi: 10.1161/CIRCRESAHA.117.311071.
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Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease.卡那奴单抗治疗动脉粥样硬化疾病的抗炎疗法。
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Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease.克隆性造血与动脉粥样硬化性心血管疾病风险
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Real-Time Monitoring of Nanoparticle Formation by FRET Imaging.利用荧光共振能量转移成像实时监测纳米颗粒的形成。
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