Hearn V M, Donaldson G C, Healy M J, Trotman D M
J Immunoassay. 1985;6(3):165-87. doi: 10.1080/01971528508063028.
A method is described which assesses results obtained from an ELISA system for the determination of human serum levels of IgG class antibodies to Aspergillus fumigatus. The method is used to discriminate positive from negative samples, and significant antibody activity may be reported to the clinician, relative to a reference positive control serum monitored simultaneously under the same test conditions. Antibody content is expressed as the absorbance of a certain dilution of serum. Duplicate samples were analysed at a single serum dilution and their absorbtion values obtained from a semi-automated ELISA microplate reader. These were entered into a computer programmed to convert the data into units on a logarithmic scale. In parallel experiments, ELISA results were compared with those obtained by the techniques of counterimmunoelectrophoresis and double diffusion which measure precipitating antibody of all classes. A relatively good degree of correlation between tests was found only among sera with a high level of antibody.
本文描述了一种方法,该方法用于评估酶联免疫吸附测定(ELISA)系统检测人血清中烟曲霉IgG类抗体水平所获得的结果。此方法用于区分阳性和阴性样本,并且在相同测试条件下,相对于同时监测的参考阳性对照血清,可将显著的抗体活性报告给临床医生。抗体含量以血清特定稀释度的吸光度表示。在单一血清稀释度下对重复样本进行分析,并使用半自动ELISA酶标仪获取其吸光度值。将这些值输入计算机程序,该程序可将数据转换为对数尺度的单位。在平行实验中,将ELISA结果与通过对流免疫电泳和双向扩散技术获得的结果进行比较,后两种技术用于检测所有类别的沉淀抗体。仅在抗体水平较高的血清中,发现不同检测方法之间具有相对较好的相关性。