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使用酶联免疫吸附测定法对肝素依赖性抗体进行特异性定量以诊断肝素相关性血小板减少症。

Specific quantification of heparin-dependent antibodies for the diagnosis of heparin-associated thrombocytopenia using an enzyme-linked immunosorbent assay.

作者信息

Gruel Y, Rupin A, Darnige L, Moalic-Reverdiau P, Poumier-Gaschard P, Binet C, Bardos P, Leroy J

机构信息

Laboratoire d'Hématologie, Faculté de Médecine, Tours, France.

出版信息

Thromb Res. 1991 Jun 1;62(5):377-87. doi: 10.1016/0049-3848(91)90011-k.

Abstract

In order to specifically detect heparin-dependent antibodies in patients with suspected heparin-associated thrombocytopenia (HAT), an adapted ELISA test was developed. Serum-platelet bindable IgG (SPb-IgG) were measured in the absence and in the presence of heparin in the sera from a/ 25 normal controls, 25 patients treated by heparin without thrombocytopenia, 29 thrombocytopenic patients not receiving heparin and b/ 12 patients with confirmed HAT. In the absence of heparin, the 12 HAT sera showed normal or elevated SPb-IgG levels (range = 10.4-36 Arbitrary Units or AU) as compared to healthy controls (8-17.1 AU). After coincubation of HAT sera with heparin (0.25, 0.50, 0.75, and 1 IU/ml), SPb-IgG levels were consistently elevated (range = 22.8-150 AU), and this increase in IgG binding (equal in mean to 200%) was always inhibited with 5 IU/ml of heparin. In contrast, a mean maximum increase in SPblgG levels of only 20% was registered in all control groups whatever the tested heparin concentration. Thus, this ELISA allows the specific diagnosis of HAT by demonstrating a serum IgG binding on platelets only in the presence of therapeutic concentrations of heparin.

摘要

为了特异性检测疑似肝素相关性血小板减少症(HAT)患者体内的肝素依赖性抗体,开发了一种改良的ELISA检测方法。检测了a/25名正常对照、25名接受肝素治疗但未出现血小板减少的患者、29名未接受肝素治疗的血小板减少患者以及b/12名确诊为HAT的患者血清中在有无肝素存在情况下的血清-血小板可结合IgG(SPb-IgG)。在无肝素情况下,与健康对照(8 - 17.1任意单位或AU)相比,12份HAT血清显示SPb-IgG水平正常或升高(范围 = 10.4 - 36任意单位或AU)。将HAT血清与肝素(0.25、0.50、0.75和1 IU/ml)共同孵育后,SPb-IgG水平持续升高(范围 = 22.8 - 150 AU),且这种IgG结合的增加(平均等于200%)总是被5 IU/ml的肝素抑制。相比之下,无论测试的肝素浓度如何,所有对照组中SPbIgG水平的平均最大增幅仅为20%。因此,这种ELISA方法通过仅在治疗浓度的肝素存在时证明血清IgG与血小板结合,从而实现对HAT的特异性诊断。

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