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针对动脉粥样硬化的疫苗研发二十年。

Two decades of vaccine development against atherosclerosis.

作者信息

Moreno-Gonzalez Miguel A, Ortega-Rivera Oscar A, Steinmetz Nicole F

机构信息

Department of NanoEngineering, University of California-San Diego, La Jolla, CA 92039, USA.

Center for Nano-ImmunoEngineering, University of California-San Diego, La Jolla, CA 92039, USA.

出版信息

Nano Today. 2023 Jun;50. doi: 10.1016/j.nantod.2023.101822. Epub 2023 Mar 31.

DOI:10.1016/j.nantod.2023.101822
PMID:37860053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10586238/
Abstract

Atherosclerosis is an immune-mediated chronic inflammatory disease that leads to the development of fatty plaques in the arterial walls, ultimately increasing the risk of thrombosis, stroke, and myocardial infarction. The immune response in this complex disease is both atheroprotective and pro-atherogenic, involving both innate and adaptive immunity. Current treatments include the adjustment of lifestyle factors, cholesterol-lowering drugs such as statins, and immunotherapy, whereas vaccine development has received comparatively little attention. In this review, we discuss the potential of antigen-specific vaccination as a preventative approach based on more than 20 years of research and innovation. Vaccination targets include proteins that are more abundant in atherosclerotic patients, such as oxidized low-density lipoprotein (LDL), apolipoprotein B-100, proprotein convertase subtilisin/kexin type-9 serine protease (PCSK9), cholesteryl ester transfer protein (CETP), and heat shock proteins HSP60 and HSP65. Immunization with such proteins or their peptide epitopes has been shown to induce T-cell activation, produce antigen-specific antibodies, reduce the size of atherosclerotic lesions, and/or reduce serum cholesterol levels. Vaccination against atherosclerosis therefore offers a new strategy to address the burden on healthcare systems caused by cardiovascular disease, the leading cause of death worldwide.

摘要

动脉粥样硬化是一种免疫介导的慢性炎症性疾病,会导致动脉壁上形成脂肪斑块,最终增加血栓形成、中风和心肌梗死的风险。在这种复杂疾病中的免疫反应既具有抗动脉粥样硬化作用,也具有促动脉粥样硬化作用,涉及固有免疫和适应性免疫。目前的治疗方法包括调整生活方式因素、使用他汀类等降胆固醇药物以及免疫疗法,而疫苗研发相对受到的关注较少。在这篇综述中,我们基于20多年的研究与创新,讨论抗原特异性疫苗接种作为一种预防方法的潜力。疫苗接种靶点包括在动脉粥样硬化患者中含量更高的蛋白质,如氧化型低密度脂蛋白(LDL)、载脂蛋白B-100、前蛋白转化酶枯草溶菌素/kexin 9型丝氨酸蛋白酶(PCSK9)、胆固醇酯转运蛋白(CETP)以及热休克蛋白HSP60和HSP65。用这些蛋白质或其肽表位进行免疫已被证明可诱导T细胞活化、产生抗原特异性抗体、减小动脉粥样硬化病变的大小和/或降低血清胆固醇水平。因此,针对动脉粥样硬化的疫苗接种为应对心血管疾病给全球主要死因的医疗系统带来的负担提供了一种新策略。

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1
Two decades of vaccine development against atherosclerosis.针对动脉粥样硬化的疫苗研发二十年。
Nano Today. 2023 Jun;50. doi: 10.1016/j.nantod.2023.101822. Epub 2023 Mar 31.
2
The AT04A vaccine against proprotein convertase subtilisin/kexin type 9 reduces total cholesterol, vascular inflammation, and atherosclerosis in APOE*3Leiden.CETP mice.抗前蛋白转化酶枯草溶菌素 9 型疫苗 AT04A 可降低 APOE*3Leiden.CETP 小鼠的总胆固醇、血管炎症和动脉粥样硬化。
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PCSK9 inhibition fails to alter hepatic LDLR, circulating cholesterol, and atherosclerosis in the absence of ApoE.在缺乏载脂蛋白E的情况下,前蛋白转化酶枯草溶菌素9(PCSK9)抑制作用无法改变肝脏低密度脂蛋白受体、循环胆固醇及动脉粥样硬化情况。
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4
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Anti-Atherogenic Mechanisms and Therapies.抗动脉粥样硬化机制与疗法
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Mitigating atherosclerosis: Integrating vaccines with gene targets.减轻动脉粥样硬化:将疫苗与基因靶点相结合。
Am Heart J Plus. 2025 Aug 6;57:100588. doi: 10.1016/j.ahjo.2025.100588. eCollection 2025 Sep.
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PCSK9 Inhibitors: A Potential Priority Choice for Lipid Management in Patients with Diabetic Kidney Disease.前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂:糖尿病肾病患者脂质管理的潜在优先选择
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A prometabolite strategy inhibits cardiometabolic disease in an ApoE-/- murine model of atherosclerosis.一种前代谢物策略在载脂蛋白E基因敲除小鼠动脉粥样硬化模型中抑制心脏代谢疾病。
JCI Insight. 2025 Aug 8;10(15). doi: 10.1172/jci.insight.191090.
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Targeted drug delivery systems for atherosclerosis.用于动脉粥样硬化的靶向给药系统。
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本文引用的文献

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A single-dose Qβ VLP vaccine against S100A9 protein reduces atherosclerosis in a preclinical model.一种针对S100A9蛋白的单剂量Qβ病毒样颗粒疫苗可在临床前模型中减轻动脉粥样硬化。
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The why and how of adaptive immune responses in ischemic cardiovascular disease.缺血性心血管疾病中适应性免疫反应的原因及机制
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MDA-LDL vaccination induces athero-protective germinal-center-derived antibody responses.MDA-LDL 疫苗接种可诱导动脉粥样硬化保护生发中心衍生的抗体应答。
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Immunization using ApoB-100 peptide-linked nanoparticles reduces atherosclerosis.使用载有 ApoB-100 肽的纳米颗粒进行免疫接种可减少动脉粥样硬化。
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Vaccine targeting ANGPTL3 ameliorates dyslipidemia and associated diseases in mouse models of obese dyslipidemia and familial hypercholesterolemia.针对 ANGPTL3 的疫苗可改善肥胖血脂异常和家族性高胆固醇血症小鼠模型中的血脂异常和相关疾病。
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PCSK9 immunization using nanoliposomes: preventive efficacy against hypercholesterolemia and atherosclerosis.使用纳米脂质体进行前蛋白转化酶枯草溶菌素9免疫:对高胆固醇血症和动脉粥样硬化的预防效果
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A VLP-based vaccine targeting ANGPTL3 lowers plasma triglycerides in mice.一种基于 VLP 的靶向 ANGPTL3 的疫苗可降低小鼠血浆中的甘油三酯。
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Pre-Clinical Evaluation of the Nanoliposomal antiPCSK9 Vaccine in Healthy Non-Human Primates.纳米脂质体抗PCSK9疫苗在健康非人类灵长类动物中的临床前评估
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In vivo CRISPR base editing of PCSK9 durably lowers cholesterol in primates.体内 CRISPR 碱基编辑持久降低灵长类动物的 PCSK9 胆固醇。
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