Verbruggen B, Novakova I, Wessels H, Boezeman J, van den Berg M, Mauser-Bunschoten E
Central Laboratory for Haematology, University Hospitalk St. Radboud, Nijmegen, The Netherlands.
Thromb Haemost. 1995 Feb;73(2):247-51.
Antibodies against factor VIII coagulant activity can appear in haemophiliacs who are treated with factor VIII preparations but also spontaneously in non-haemophiliacs. The Bethesda assay is the most commonly used method to detect these antibodies, but it lacks specificity especially in the lower range resulting in unreliable data. Two modifications are proposed and tested to resolve the imperfections: 1. Buffering the normal plasma used in the assay- and control mixture with 0.1 M imidazole to pH 7.4. 2. Replacing the imidazole buffer in the control mixture by immunodepleted factor VIII deficient plasma. These modifications allow better discrimination between positive and negative samples and improve reliability.
针对凝血因子 VIII 促凝活性的抗体可出现在接受凝血因子 VIII 制剂治疗的血友病患者中,也可在非血友病患者中自发出现。贝塞斯达检测法是检测这些抗体最常用的方法,但它缺乏特异性,尤其是在较低水平时,导致数据不可靠。本文提出并测试了两种改进方法以解决这些缺陷:1. 用 0.1 M 咪唑将检测和对照混合物中使用的正常血浆缓冲至 pH 7.4。2. 用免疫耗尽的 VIII 因子缺乏血浆替代对照混合物中的咪唑缓冲液。这些改进能够更好地区分阳性和阴性样本,并提高可靠性。