Moake J L
Baylor College of Medicine, Houston, Texas, USA.
Thromb Haemost. 1995 Jul;74(1):240-5.
Recent studies indicate that CRTTP patients have excessive shear stress-induced platelet aggregation that is associated with the presence of ULvWF multimers in their plasma and increased vWF-binding to their platelets by flow cytometry. In these CRTTP patients, relapses, excessive shear-aggregation and the presence in their plasma of ULvWF forms are all reversed by the infusion of normal FFP or substances devoid of the largest vWF multimers found in plasma (cryoprecipitate-poor plasma or cryosupernatant; solvent/detergent-treated plasma) without the need for concurrent plasmapheresis. This constellation of observations, along with reports of increased vWF in TTP platelet thrombi, increases the probability that ULvWF multimers derived from injured or abnormal endothelial cells induce aggregation during TTP episodes in high-shear regions of the microcirculation.
最近的研究表明,慢性复发性血栓性血小板减少性紫癜(CRTTP)患者存在过度的剪切应力诱导的血小板聚集,这与他们血浆中超大分子量血管性血友病因子(ULvWF)多聚体的存在以及通过流式细胞术检测到的血管性血友病因子(vWF)与血小板结合增加有关。在这些CRTTP患者中,复发、过度的剪切诱导聚集以及血浆中ULvWF形式的存在,均可通过输注正常新鲜冰冻血浆(FFP)或缺乏血浆中发现的最大vWF多聚体的物质(少冷沉淀血浆或冷上清液;溶剂/去污剂处理的血浆)而逆转,无需同时进行血浆置换。这一系列观察结果,连同有关血栓性血小板减少性紫癜(TTP)血小板血栓中vWF增加的报道,增加了以下可能性:在微循环的高剪切区域,源自受损或异常内皮细胞的ULvWF多聚体在TTP发作期间诱导聚集。