Schwameis Michael, Schörgenhofer Christian, Assinger Alice, Steiner Margarete M, Jilma Bernd
Bernd Jilma, MD, Department of Clinical Pharmacology, Medical University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria, Tel.: +43 1 40400 29810, Fax: +43 1 40400 29990, E-mail:
Thromb Haemost. 2015 Apr;113(4):708-18. doi: 10.1160/TH14-09-0731. Epub 2014 Dec 11.
Absent or severely diminished activity of ADAMTS13 (A Disintegrin And Metalloprotease with a ThromboSpondin type 1 motif, member 13) resulting in the intravascular persistence and accumulation of highly thrombogenic ultra large von Willebrand factor (UL-VWF) multimers is the pathophysiological mechanism underlying thrombotic thrombocytopenic purpura. Reduced VWF-cleaving protease levels, however, are not uniquely restricted to primary thrombotic microangiopathy (TMA), e. g. thrombotic thrombocytopenic purpura, but also occur in other life-threatening thrombocytopenic conditions: severely decreased ADAMTS13 activity is seen in severe sepsis, disseminated intravascular coagulation (DIC) and complicated malarial infection. The clinical relevance of these secondary thrombotic microangiopathies is increasingly recognised, but its therapeutic implications have not yet been determined. The presence of a secondary TMA in certain diseases may define patient groups which possibly could benefit from ADAMTS13 replacement or a VWF-targeting therapy. This short-review focuses on the role of UL-VWF multimers in secondary TMA and discusses the potential of investigational therapies as candidates for the treatment of TTP. In conclusion, prospective clinical trials on the effectiveness of protease replacementin vivo seem reasonable. Carefully selected patients with secondary TMA may benefit from therapies primarily intended for the use in patients with TTP.
ADAMTS13(含Ⅰ型血小板反应蛋白基序的解聚素和金属蛋白酶13)活性缺乏或严重降低,导致具有高度血栓形成性的超大血管性血友病因子(UL-VWF)多聚体在血管内持续存在和蓄积,这是血栓性血小板减少性紫癜的病理生理机制。然而,VWF裂解蛋白酶水平降低并非原发性血栓性微血管病(TMA)所特有,例如血栓性血小板减少性紫癜,在其他危及生命的血小板减少性疾病中也会出现:在严重脓毒症、弥散性血管内凝血(DIC)和复杂的疟疾感染中可见ADAMTS13活性严重降低。这些继发性血栓性微血管病的临床相关性日益受到认可,但其治疗意义尚未确定。某些疾病中继发性TMA的存在可能界定了可能从ADAMTS13替代治疗或VWF靶向治疗中获益的患者群体。这篇简短综述聚焦于UL-VWF多聚体在继发性TMA中的作用,并讨论了作为血栓性血小板减少性紫癜治疗候选药物的研究性疗法的潜力。总之,关于蛋白酶替代疗法在体内有效性的前瞻性临床试验似乎是合理的。精心挑选的继发性TMA患者可能会从主要用于血栓性血小板减少性紫癜患者的疗法中获益。