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一种用于检测红细胞结合免疫球蛋白的定量酶联免疫吸附测定法。

A quantitative ELISA for measuring red cell-bound immunoglobulins.

作者信息

Hazlehurst D D, Hudson G, Sokol R J

机构信息

National Blood Service, Trent Centre, Sheffield, UK.

出版信息

Acta Haematol. 1996;95(2):112-6. doi: 10.1159/000203858.

Abstract

An ELISA was developed for quantitating red-cell-bound IgG and IgA and its feasibility assessed on 50 blood donations and 32 clinical specimens with raised cell-bound IgG. Test and quality control samples and immunoglobulin standards (in red-cell lysate buffer) were assayed together. Calibration curves were derived from the standards, test values being read off and related to cell count. The working range was around 5-70 ng/ml, the upper limit being indefinitely extendable by dilution with lysate buffer. Ranges of results (and medians) in molecules per red cell were < 26-240 (40) for IgG and < 29-94 ( < 29) for IgA in the donations with 240-62,700 (1,200) for IgG and < 29-4,500 (73) for IgA in the clinical specimens. The method which can be adapted for any cell-bound immunoprotein should be particularly valuable in investigating autoimmune haemolysis.

摘要

开发了一种酶联免疫吸附测定法(ELISA)用于定量红细胞结合的IgG和IgA,并在50份献血样本和32份红细胞结合IgG升高的临床样本上评估了其可行性。测试样本、质量控制样本和免疫球蛋白标准品(在红细胞裂解缓冲液中)一起进行检测。根据标准品得出校准曲线,从校准曲线上读取测试值并与细胞计数相关联。工作范围约为5-70 ng/ml,上限可通过用裂解缓冲液稀释无限扩展。献血样本中,每红细胞分子的结果范围(及中位数)对于IgG为<26-240(40),对于IgA为<29-94(<29);临床样本中,对于IgG为240-62,700(1,200),对于IgA为<29-4,500(73)。该方法可适用于任何细胞结合的免疫蛋白,在自身免疫性溶血的研究中应具有特别重要的价值。

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