Anantharamaiah G M, Goldberg Dennis
Department of Medicine, Biochemistry & Molecular Genetics; University of Alabama at Birmingham, Birmingham, AL 35294, USA.
LipimetiX Development, LLC, Natick, MA 01760, USA.
Clin Lipidol. 2015 Jan 1;10(1):83-90. doi: 10.2217/clp.14.63.
Despite wide use of statins, significant cardiovascular disease risk persists. High-density lipoprotein based therapy has not yielded any positive results in combating this disease. Newer methods to rapidly decrease plasma cholesterol are much needed. While apolipoprotein B is a ligand for low-density lipoprotein receptor, which clears low-density lipoprotein cholesterol in a highly regulated pathway, apolipoprotein E (apoE) is a ligand for clearing other apolipoprotein B containing atherogenic lipoproteins via an alternate receptor pathway, especially the heparin sulfate proteoglycans on the liver cell surface. We describe here a novel method that replaces apoE as a ligand to clear all of the atherogenic lipoproteins via the heparin sulfate proteoglycans pathway. This ligand replacement apoE mimetic peptide therapy, having been designated as an orphan drug by the US FDA, is in clinical trials.
尽管他汀类药物被广泛使用,但心血管疾病的重大风险依然存在。基于高密度脂蛋白的疗法在对抗这种疾病方面尚未取得任何积极成果。因此,迫切需要新的方法来快速降低血浆胆固醇。载脂蛋白B是低密度脂蛋白受体的配体,可通过高度调控的途径清除低密度脂蛋白胆固醇,而载脂蛋白E(apoE)则是通过另一种受体途径,特别是肝细胞表面的硫酸乙酰肝素蛋白聚糖,来清除其他含载脂蛋白B的致动脉粥样硬化脂蛋白的配体。我们在此描述一种新方法,该方法通过硫酸乙酰肝素蛋白聚糖途径替代apoE作为配体,以清除所有致动脉粥样硬化脂蛋白。这种配体替代apoE模拟肽疗法已被美国食品药品监督管理局指定为孤儿药,正在进行临床试验。