Haraj Alireza, Bakhshandeh Masoomeh, Shokri Nafiseh, Shariat Rad Prand, Alyan Ali, Chegini Zahra, Nazari Mohammad Ali, Taji Seyed Parsa Seyedi, Najafi Mohammad
Student Research Committee, Faculty of Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Clinical Biochemistry Department, Faculty of Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Am Heart J Plus. 2025 Aug 6;57:100588. doi: 10.1016/j.ahjo.2025.100588. eCollection 2025 Sep.
The formation and progression of atherosclerotic plaques occur through cellular dysfunction and remodeling of the extracellular matrix in the sub-endothelial space of vessels. The immunity against specific antigens is suggested to mitigate the atherosclerosis process. Primarily, studies have suggested that certain antigens, such as ox-LDL, ApoB-100, CETP, PCSK9, HSP60, MHC-II-derived peptides, and interleukins, are involved in atherosclerosis. However, recognizing the intricate interplay between immune responses and the formation of arterial plaques is essential to optimize immunization against atherosclerosis. In this review, the roles of some genes were presented in triggering atherosclerotic plaque events. Furthermore, some immunization approaches are presented to target these genes. The studies suggested that vaccination against the progression of atherosclerosis is an essential and effective approach to reducing the high death rate in autoimmune diseases.
动脉粥样硬化斑块的形成和进展是通过血管内皮下空间的细胞功能障碍和细胞外基质重塑而发生的。针对特定抗原的免疫作用被认为可以减轻动脉粥样硬化进程。首先,研究表明某些抗原,如氧化低密度脂蛋白(ox-LDL)、载脂蛋白B-100(ApoB-100)、胆固醇酯转运蛋白(CETP)、前蛋白转化酶枯草溶菌素9(PCSK9)、热休克蛋白60(HSP60)、主要组织相容性复合体II类(MHC-II)衍生肽和白细胞介素,都与动脉粥样硬化有关。然而,认识到免疫反应与动脉斑块形成之间复杂的相互作用对于优化抗动脉粥样硬化免疫至关重要。在这篇综述中,介绍了一些基因在引发动脉粥样硬化斑块事件中的作用。此外,还介绍了一些针对这些基因的免疫方法。研究表明,针对动脉粥样硬化进展的疫苗接种是降低自身免疫性疾病高死亡率的一种重要且有效的方法。