Cerilli J, Brasile L, Karmody A
Ann Surg. 1985 Sep;202(3):329-34. doi: 10.1097/00000658-198509000-00009.
An autoantibody directed against an antigen system that is expressed on the vascular endothelial cell (VEC) was recently identified in random patients with peripheral vascular disease. This VEC antigen system is also present on the peripheral blood monocyte but not on any other cell type studied to date. In a randomized study of 112 patients with peripheral vascular disease at the Albany Medical College, 46% demonstrated an autoantibody against their autologous monocytes and VEC. This autoantibody is a highly cytotoxic, complement-fixing antibody directed against VEC antigens. It does not crossreact with autologous T or B lymphocytes and appears to be highly polymorphic. It is present in only nine per cent of the age-matched controls and was never detected in young controls. This preliminary investigation suggests that immunological injury may be the initiating factor in the development of atherosclerotic lesions more frequently than currently appreciated. Whether this autoantibody to VEC is the result of or the cause of endothelial cell damage in these patients is still under study.
最近,在随机选取的外周血管疾病患者中发现了一种针对在血管内皮细胞(VEC)上表达的抗原系统的自身抗体。这种VEC抗原系统在外周血单核细胞中也存在,但在迄今研究的任何其他细胞类型中都不存在。在奥尔巴尼医学院对112例外周血管疾病患者进行的一项随机研究中,46%的患者表现出针对其自身单核细胞和VEC的自身抗体。这种自身抗体是一种针对VEC抗原的高细胞毒性、补体结合抗体。它不与自身T或B淋巴细胞发生交叉反应,似乎具有高度多态性。它仅存在于9%的年龄匹配对照中,在年轻对照中从未检测到。这项初步研究表明,免疫损伤可能比目前所认识到的更频繁地是动脉粥样硬化病变发展的起始因素。这种针对VEC的自身抗体是这些患者内皮细胞损伤的结果还是原因仍在研究中。