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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Heat treatment of samples improve the performance of the Nijmegen-Bethesda assay in hemophilia A patients undergoing immune tolerance induction
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Heat treatment of samples improve the performance of the Nijmegen-Bethesda assay in hemophilia A patients undergoing immune tolerance induction

机译:样品的热处理可提高Nijmegen-Bethesda检测在接受免疫耐受诱导的血友病A患者中的性能

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Nijmegen-Bethesda assay is the gold standard to assess inhibitory antibodies against factor (F) VIII. This method has some limitations, including high coefficient of variation and possible interference of residual endogenous or exogenous factor VIII. Heat-treatment of samples at 56 degrees C for 30 min could be a strategy to improve the sensitivity of this test. The aim of this study was to compare inhibitor quantification in hemophilia patients with and without inhibitor performed in previously heated and non-heated samples. A total of 109 analyses from 46 patients with severe hemophilia A were performed. Patients were divided into three groups: 20 patients with no history of inhibitor, recently and not recently exposed to FVIII (group I), 21 patients with history of inhibitor not exposed to FVIII (group II), and 5 patients (68 samples) undergoing an immune tolerance induction (ITI) protocol (group III). For patients with no history of inhibitor, heat-treatment did not modify the results (p= 0.24). However, differences in inhibitor levels between heated and non-heated samples were observed in patients with history of inhibitor (group II, p < 0.05) and in patients in ITI (group III, p < 0.001). In 11 samples, inhibitor quantification shifted from negative to positive. Additionally, a longitudinal evaluation of each ITI patient showed similar trend line for the results of heated and non-heated samples. In this study, we demonstrated that heating samples increase sensitivity of Nijmegen-Bethesda assay, with no shift from negative to positive results in patients with no history of inhibitor. Furthermore, this procedure has an important role to patients undergoing an ITI protocol. (C) 2015 Elsevier Ltd. All rights reserved.
机译:奈梅亨-贝塞斯达测定法是评估针对因子(F)VIII的抑制性抗体的金标准。该方法有一些局限性,包括高变异系数以及可能残留的内源性或外源性因子VIII的干扰。在56摄氏度下对样品进行30分钟的热处理可能是提高该测试灵敏度的一种策略。这项研究的目的是比较血友病患者在先前加热和未加热样品中是否进行抑制剂治疗时的抑制剂定量。从46例重度A型血友病患者中总共进行了109次分析。患者分为三组:20例无抑制剂史,近期和近期未接触过FVIII的患者(I组),21例具有抑制剂史不接触FVIII的患者(II组)和5例(68个样本)免疫耐受诱导(ITI)方案(第III组)。对于没有抑制剂史的患者,热处理不会改变结果(p = 0.24)。然而,在有抑制剂病史的患者(II组,p <0.05)和ITI患者(III组,p <0.001)中观察到加热样品和未加热样品之间的抑制剂水平差异。在11个样品中,抑制剂的定量从负数变为正数。此外,对每个ITI患者的纵向评估显示,加热样品和未加热样品的结果趋势线相似。在这项研究中,我们证明了加热样品可以提高奈梅亨-贝塞斯达(Nijmegen-Bethesda)测定的灵敏度,对于没有抑制剂史的患者,其结果不会从阴性转变为阳性。此外,该程序对接受ITI协议的患者也具有重要作用。 (C)2015 Elsevier Ltd.保留所有权利。

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