一种检测血友病患者因子VIII抑制抗体的新型ELISA筛选试验的评价。

P. G. Martin, K. Sukhu, E. Chambers, P. Giangrande
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引用次数: 30

摘要

用凝血因子浓缩液治疗A型血友病患者可能导致产生针对凝血因子VIII (FVIII)的抑制性抗体。在这项研究中,一项先前未发表的FVIII抑制剂筛选ELISA检测(基因检测研究所[GTI] FVIII抑制剂,Brookfield, WI, USA)在131份血液样本中进行了评估(124份来自a型血友病患者,7份来自获得性FVIII抑制剂患者的连续样本)。与常规筛选法(基于FVIII的回收率)进行比较,并与新牛津法确认阳性(回收率< 90%)。ELISA试剂盒的敏感性为97.7%,特异性为78.4%。这项新检测的高阴性预测值(98.6%)表明,它可能是一种可靠、快速(< 2小时)和灵活(微孔条格式)的工具,可用于筛查a型血友病患者和疑似获得性FVIII抑制剂患者的样本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs.
Treatment of patients with haemophilia A with coagulation factor concentrates may result in the development of inhibitory antibodies directed against factor VIII (FVIII). In this study, a previously unpublished ELISA test for FVIII inhibitor screening (Genetic Testing Institute [GTI] FVIII inhibitor, Brookfield, WI, USA) was evaluated in 131 blood samples (124 samples from patients with haemophilia A, and seven serial samples from one patient with an acquired FVIII inhibitor). Comparisons were made with the routine screening assay (based on recovery of FVIII) and confirmed where positive (< 90% recovery) with the New Oxford assay. The ELISA kit had a sensitivity of 97.7% and specificity of 78.4%. The high negative predictive value of this new test (98.6%) suggests it may be useful as a reliable, rapid (< 2 h) and flexible (microwell strip format) tool for inhibitor screening of samples from both patients with haemophilia A and those with suspected acquired FVIII inhibitors.
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