Kurata Y, Tomiyama Y
Department of Blood Transfusion, Osaka University Hospital.
Nihon Rinsho. 1992 Feb;50(2):287-91.
The effect of anti-platelet antibodies, including murine monoclonal antibodies, autoantibodies and alloantibodies, on platelet function was analyzed. The target antigen of these antiplatelet antibodies, investigated in the present study, was a glycoprotein IIb/IIIa, which is a receptor of fibrinogen and plays an important role in platelet aggregation. Some of these antibodies inhibited agonist-induced platelet aggregation. The target antigen of one murine monoclonal antibodies, designated OP-G2, was a glycoprotein IIb/IIIa and interestingly, this antibody induced platelet aggregation, which required divalent cation and fibrinogen. We compared the epitope of these antibodies by inhibition assay and found the epitope of these antibodies to be very close. The binding of OP-G2 to the platelets required Ca2+. These data suggest that OP-G2 recognizes an epitope at or in very close proximity to the fibrinogen binding site of GPIIb/IIIa, as compared with other antibodies.
分析了包括鼠单克隆抗体、自身抗体和同种抗体在内的抗血小板抗体对血小板功能的影响。本研究中所研究的这些抗血小板抗体的靶抗原是糖蛋白IIb/IIIa,它是纤维蛋白原的受体,在血小板聚集中起重要作用。其中一些抗体抑制激动剂诱导的血小板聚集。一种名为OP-G2的鼠单克隆抗体的靶抗原是糖蛋白IIb/IIIa,有趣的是,这种抗体诱导血小板聚集,这需要二价阳离子和纤维蛋白原。我们通过抑制试验比较了这些抗体的表位,发现这些抗体的表位非常接近。OP-G2与血小板的结合需要Ca2+。这些数据表明,与其他抗体相比,OP-G2识别GPIIb/IIIa纤维蛋白原结合位点处或非常接近该位点的一个表位。