Moreno-Gonzalez Miguel A, Ortega-Rivera Oscar A, Steinmetz Nicole F
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.
Nano Today. 2023 Jun;50. doi: 10.1016/j.nantod.2023.101822. Epub 2023 Mar 31.
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.
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。