Soria J, Soria C, Mirshahi M, Mirshahi M, Boucheix C, Pujade E, Perrot J Y, Samama M, Bernadou A, Caen J P
C R Acad Sci III. 1987;304(11):307-11.
A specific determination of fibrin degradation product (FbDP) is essential for the monitoring of thrombolytic therapy. In patients under thrombolytic therapy, even with tpA (tissue type plasminogen activator) fibrinogen is degraded, and fragment D derived from fibrinogen degradation, is evidenced in the plasma of treated patients. In order to determine specifically the FbDP, even in the presence of fragment D, we take into account the fact that FbDP are complexes such as DDE complex. Therefore a new Elisa technique is proposed. FbDP and fragment D are captured from plasma by immobilized anti D neo monoclonal antibody which recognizes an epitope accessible on fragment D but does not react with undegraded fibrinogen. DDE complexes are then detected specifically using a peroxidase-labelled anti E antibody. The advantage of this technique is discussed in this paper.
纤维蛋白降解产物(FbDP)的特异性测定对于监测溶栓治疗至关重要。在接受溶栓治疗的患者中,即使使用组织型纤溶酶原激活剂(tpA),纤维蛋白原也会被降解,并且在接受治疗患者的血浆中可检测到源自纤维蛋白原降解的D片段。为了特异性测定FbDP,即使存在D片段,我们考虑到FbDP是诸如DDE复合物之类的复合物这一事实。因此,提出了一种新的酶联免疫吸附测定(ELISA)技术。通过固定化抗D新单克隆抗体从血浆中捕获FbDP和D片段,该抗体识别D片段上可及的表位,但不与未降解的纤维蛋白原反应。然后使用过氧化物酶标记的抗E抗体特异性检测DDE复合物。本文讨论了该技术的优点。