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作 者:李振宇[1] 赵益明[1] 董宁征[1] 沈飞[1] 阮长耿[1]
机构地区:[1]苏州大学附属第一医院、江苏省血液研究所卫生部血栓与止血重点实验室,215006
出 处:《中华血液学杂志》2009年第3期154-157,共4页Chinese Journal of Hematology
摘 要:目的 制备并鉴定抗凝血因子Ⅷ(FⅧ)C2区单克隆抗体(单抗),研究其对FⅧ活性的影响。方法体外表达rFⅧC2区蛋白,免疫BALB/c小鼠制备鼠源性单抗。不同剂量的单抗与正常人新鲜混合血浆孵育后测定FⅧ活性及活化部分凝血活酶时间(APTT)等;ELISA法测定该单抗对rhFⅧ与血管性血友病因子(vWF)、磷脂酰丝氨酸(PS)及血小板结合实验的影响。结果获得一株抗FⅧC2区单抗,命名为SZ-132。与血浆孵育后呈剂量依赖方式抑制FⅧ活性,APTT明显延长;抗体浓度超过25μg/ml时,FⅧ活性为0;该抗体能够抑制rhFⅧ-vWF、rhFⅧ-PW及rhFⅧ与血小板的结合。结论SZ-132是一株特异性针对FⅧC2区的抑制性单抗。Objective To develop a monoclonal antibody (mAb) directed to Fvm C2 domain and investigate its effect on FⅧ activity. Methods FⅧ C2 protein was expressed in E. coli and purified. A murine antihuman FⅧ C2 domain mAb SZ-132 was developed by standard hybridoma technology and characterized. In coagulation assays, different concentrations of SZ-132 were incubated with freshly collected pooled human plasma and the residual activity of FⅧ and activated partial thromboplastin time (AFTT) were determined. The effects of SZ-132 on rhFⅧ binding to purified human vWF, phosphatidylserine (PS) and platelets were assessed by enzyme linked immunosorbent assays (ELISA). Results SZ-132 could inhibit FⅧ procoagulant activity in a dose-dependent manner within the concentrations of 0 - 25μg/ml and the FⅧ activity was completely inhibited on above 25μg/ml. It could also prevent rhFVm from binding to vWF, PS and platelets. Conclusions SZ-132 is a neutralizing mAb against Fvm C2 domain and can inhibit FⅧ procoagulant activity by preventing FⅧ from binding to vWF and PS.
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