血小板
单克隆抗体
组织因子
抗体
血栓形成
单核细胞
病理生理学
单克隆
免疫学
化学
内科学
医学
内分泌学
凝结
作者
Joan Carles Reverter,Dolors Tàssies,Josep Font,Munther A. Khamashta,Kenji Ichikawa,Ricard Cervera,Ginés Escolar,Graham Hughes,M Ingelmo,A Ordinas
标识
DOI:10.1002/1529-0131(199808)41:8<1420::aid-art11>3.0.co;2-u
摘要
Objective To investigate the effect of human monoclonal anticardiolipin antibodies (aCL) on platelet interaction with the subendothelium under flow conditions and on tissue factor (TF) expression on normal monocytes. Methods Three monoclonal IgM aCL (TM1B3, GR1D5, and EY2C9) and 2 affinity-purified IgM aCL were studied. Immunoglobulins were added to normal blood and perfused through chambers containing denuded vascular segments. Platelet interactions were morphometrically evaluated by determining the percentage of total surface covered by platelets (PCS) or by large aggregates of thrombi platelets (TP). Expression of TF on monocytes was measured after immunoglobulin incubation with normal mononuclear cells. Results Significant increases in the total PCS and expression of TF were observed using all aCL. Increased levels of TP were induced by all aCL except EY2C9 (obtained from a patient without thrombosis). Previous incubations of these aCL with subendothelial surfaces did not increase platelet interaction. Conclusion The effects of aCL on platelet function may help to explain the pathophysiology of thrombosis in the antiphospholipid syndrome.
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