Department of Medicine, Ohio State University, Columbus, OH.
Blood. 2018 Aug 30;132(9):903-910. doi: 10.1182/blood-2018-02-791533. Epub 2018 Jul 13.
ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin type 1 motif, 13) is a metalloprotease responsible for cleavage of ultra-large von Willebrand factor (VWF) multimers. Severely deficient activity of the protease can trigger an acute episode of thrombotic thrombocytopenic purpura (TTP). Our understanding of the pathophysiology of TTP has allowed us to grasp the important role of ADAMTS13 in other thrombotic microangiopathies (TMAs) and thrombotic disorders, such as ischemic stroke and coronary artery disease. Through its action on VWF, ADAMTS13 can have prothrombotic and proinflammatory properties, not only when its activity is severely deficient, but also when it is only moderately low. Here, we will discuss the biology of ADAMTS13 and the different assays developed to evaluate its function in the context of TTP, in the acute setting and during follow-up. We will also discuss the latest evidence regarding the role of ADAMTS13 in other TMAs, stroke, and cardiovascular disease. This information will be useful for clinicians not only when evaluating patients who present with microangiopathic hemolytic anemia and thrombocytopenia, but also when making clinical decisions regarding the follow-up of patients with TTP.
血管性血友病因子(VWF)裂解蛋白酶 13(ADAMTS13,一种含血栓反应蛋白 1 型基序的解聚素金属蛋白酶)是一种金属蛋白酶,负责裂解超大分子量的 VWF 多聚体。该蛋白酶的活性严重缺乏可引发急性血栓性血小板减少性紫癜(TTP)。我们对 TTP 病理生理学的认识,使我们能够理解 ADAMTS13 在其他血栓性微血管病(TMA)和血栓性疾病(如缺血性脑卒中、冠状动脉疾病)中的重要作用。通过对 VWF 的作用,ADAMTS13 不仅在其活性严重缺乏时,而且在其活性仅中度降低时,具有促血栓形成和促炎特性。在这里,我们将讨论 ADAMTS13 的生物学特性,以及为评估其在 TTP 背景下、在急性发作期和随访期的功能而开发的不同检测方法。我们还将讨论 ADAMTS13 在其他 TMA、脑卒中以及心血管疾病中的作用的最新证据。这些信息不仅对评估出现微血管性溶血性贫血和血小板减少的患者的临床医生有用,而且对 TTP 患者的随访临床决策也有用。