Santoso S, Kiefel V, Mueller-Eckhardt C
Institute of Clinical Immunology and Blood Transfusion, Justus-Liebig-University, Giessen, FRG.
Thromb Haemost. 1987 Oct 28;58(3):866-71.
The redistribution of platelet glycoproteins (GP) Ib, IIb and IIIa in response to stimulation with human platelet specific alloantibodies, autoantibodies and a quinidine-dependent antibody was investigated using immunofluorescence and a quantitative radioimmunoassay. The platelet GPs carrying the corresponding epitopes were determined using immunoblot technique or radioimmunoprecipitation. In accordance with previous results obtained with murine monoclonal platelet specific antibodies, redistribution upon stimulation with human platelet reactive antibodies was observed only due to reactions with epitopes on GP IIb, IIIa, respectively, but not on GP Ib. We therefore believe that membrane redistribution of human platelets induced by various antibodies is a function of the GP recognized by those antibodies rather than the source of the platelet reactive antibody.
利用免疫荧光和定量放射免疫测定法,研究了血小板糖蛋白(GP)Ib、IIb和IIIa在人血小板特异性同种抗体、自身抗体和奎尼丁依赖性抗体刺激下的重新分布情况。使用免疫印迹技术或放射免疫沉淀法确定携带相应表位的血小板糖蛋白。与先前用鼠单克隆血小板特异性抗体获得的结果一致,在用人类血小板反应性抗体刺激后观察到的重新分布仅分别是由于与GP IIb、IIIa上的表位反应,而不是与GP Ib上的表位反应。因此,我们认为各种抗体诱导的人血小板膜重新分布是这些抗体所识别的糖蛋白的功能,而不是血小板反应性抗体的来源。