首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura.
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Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura.

机译:血栓性血小板减少性紫癜患者血浆治疗后von Willebrand因子裂解蛋白酶的恢复和半衰期。

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摘要

Plasma exchange using fresh-frozen plasma (FFP) for replacement was given to two brothers during a relapse of thrombotic thrombocytopenic purpura (TTP). A constitutional deficiency of von Willebrand factor(vWF)-cleaving protease had been previously established in both patients. No inhibitor of vWF-cleaving protease was present in patients' plasmas. They received plasma exchange for four and three consecutive days, respectively. In both patients, the activity of vWF-cleaving protease after the first plasmapheresis session was evaluated and was found to be virtually identical to anticipated activity calculated from predicted patient plasma volume and volume of exchanged plasma. Pathologic platelet counts and lactate dehydrogenase levels were normalized in both patients within 4-6 days. The biologic half-life of vWF-cleaving protease was determined in these patients following the last plasma exchange. The respective half-lives of 3.3 and 2.1 days represent the lowest known clearance rates of proteases in circulating human plasma. Another patient with relapsing TTP was treated with plasma exchange and/or plasma infusion for 10 consecutive days during the first relapse, 221-231 days after the initial TTP event. Pharmacokinetic studies of vWF-cleaving protease were performed after plasma exchange on day 221 and after plasma infusion on day 231. High level of an IgG in patient plasma, capable of completely inhibiting protease activity in an equal volume of normal plasma, had been established prior to first plasmapheresis. There was no measurable protease activity at any time during plasma therapy. Following plasma exchange, the level of the inhibitor was transiently slightly depressed. After 10 days of plasma therapy, the concentration of the inhibitor in patient plasma was increased about 5-fold. We suggest that, in contrast to protease deficient patients without circulating inhibitor, complementary therapy including immunosuppressive treatment, vincristine and/or splenectomy is indicated in patients with acquired inhibitors of vWF-cleaving protease. Testing for vWF-cleaving protease inhibitor may be useful in predicting the response to plasma exchange in patients with TTP.
机译:在血栓性血小板减少性紫癜(TTP)复发期间,给了两个兄弟以新鲜冷冻血浆(FFP)进行置换的血浆交换。先前已在两名患者中建立了von Willebrand因子(vWF)切割蛋白酶的体质缺乏。患者血浆中没有vWF裂解蛋白酶抑制剂。他们分别连续四天和三天接受血浆置换。在这两名患者中,均评估了第一次血浆置换后vWF裂解蛋白酶的活性,发现该活性实际上与根据预测的患者血浆量和血浆交换量计算出的预期活性相同。两名患者在4-6天内均将病理性血小板计数和乳酸脱氢酶水平标准化。在最后一次血浆置换后,在这些患者中确定了vWF裂解蛋白酶的生物学半衰期。分别为3.3天和2.1天的半衰期代表循环人体血浆中蛋白酶的最低已知清除率。 TTP复发的另一名患者在首次复发期间(即最初的TTP事件发生后的221-231天)连续10天接受血浆置换和/或血浆输注治疗。在第221天进行血浆置换后和第231天进行血浆输注后,进行了vWF裂解蛋白酶的药代动力学研究。在患者血浆中高水平的IgG能够完全抑制等体积的正常血浆中的蛋白酶活性。第一次血浆置换。在血浆治疗期间的任何时候都没有可测量的蛋白酶活性。血浆交换后,抑制剂的水平短暂降低。血浆治疗10天后,患者血浆中的抑制剂浓度增加了约5倍。我们建议,与没有循环抑制剂的缺乏蛋白酶的患者相反,在获得性vWF裂解蛋白酶抑制剂的患者中,建议进行包括免疫抑制治疗,长春新碱和/或脾切除术在内的补充疗法。 vWF切割蛋白酶抑制剂的测试可能有助于预测TTP患者对血浆交换的反应。

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