VCAM-1-targeted nanoparticles to diagnose, monitor and treat atherosclerosis.

Nanomedicine (London, England) Pub Date : 2024-04-01 Epub Date: 2024-02-29 DOI:10.2217/nnm-2023-0282
Rita Castro, James H Adair, Andrea M Mastro, Thomas Neuberger, Gail L Matters
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Abstract

Vascular cell adhesion molecule-1 (VCAM-1) was identified over 2 decades ago as an endothelial adhesion receptor involved in leukocyte recruitment and cell-based immune responses. In atherosclerosis, a chronic inflammatory disease of the blood vessels that is the leading cause of death in the USA, endothelial VCAM-1 is robustly expressed beginning in the early stages of the disease. The interactions of circulating immune cells with VCAM-1 on the activated endothelial cell surface promote the uptake of monocytes and the progression of atherosclerotic lesions in susceptible vessels. Herein, we review the role of VCAM-1 in atherosclerosis and the use of VCAM-1 binding peptides, antibodies and aptamers as targeting agents for nanoplatforms for early detection and treatment of atherosclerotic disease.

用于诊断、监测和治疗动脉粥样硬化的 VCAM-1 靶向纳米粒子。
血管细胞粘附分子-1(VCAM-1)早在二十多年前就被确认为一种内皮粘附受体,参与白细胞的招募和基于细胞的免疫反应。动脉粥样硬化是一种慢性血管炎症性疾病,是美国人死亡的主要原因,在这种疾病的早期阶段,血管内皮 VCAM-1 就开始大量表达。循环免疫细胞与活化内皮细胞表面的 VCAM-1 相互作用,促进了单核细胞的吸收和易感血管中动脉粥样硬化病变的进展。在此,我们回顾了 VCAM-1 在动脉粥样硬化中的作用,以及将 VCAM-1 结合肽、抗体和适配体作为纳米平台的靶向药物用于动脉粥样硬化疾病的早期检测和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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