Tsimikas Sotirios
Vascular Medicine Program, University of California San Diego, La Jolla 92037-0975, USA.
Curr Atheroscler Rep. 2006 Jan;8(1):55-61. doi: 10.1007/s11883-006-0065-1.
The concept that the oxidation of lipoproteins is central in the pathogenesis of atherosclerosis was first reported over 25 years ago, initially by in vitro studies and subsequently through experimental models of atherosclerosis. The innate immune system plays a key role in atherogenesis as manifested by its atherosclerosis-modulating properties, the immunogenicity of oxidized low-density lipoprotein (LDL), and the presence of oxidized LDL autoantibodies in plasma and lesions of humans. In the past 10 years it has been possible to generate monoclonal antibodies to oxidized LDL to directly measure oxidized LDL in plasma. This has led to a rapidly accelerating pace of new reports on the relationship of circulating oxidized LDL and various cardiovascular pathologic processes, which are the focus of this review.
25多年前首次报道了脂蛋白氧化在动脉粥样硬化发病机制中起核心作用这一概念,最初是通过体外研究,随后是通过动脉粥样硬化实验模型。固有免疫系统在动脉粥样硬化形成中起关键作用,这表现为其对动脉粥样硬化的调节特性、氧化型低密度脂蛋白(LDL)的免疫原性,以及在人类血浆和病变中存在氧化型LDL自身抗体。在过去10年中,已经能够产生针对氧化型LDL的单克隆抗体,以直接测量血浆中的氧化型LDL。这导致了关于循环氧化型LDL与各种心血管病理过程之间关系的新报道迅速增加,这也是本综述的重点。