Halbert S P, Bastomsky C H, Anken M
Clin Chim Acta. 1983 Jan 7;127(1):69-76. doi: 10.1016/0009-8981(83)90076-1.
A rapid, specific, standardized, objective and sensitive quantitative enzyme immunoassay (ELISA) procedure has been developed for the detection of human autoantibodies to thyroglobulin. It involves three ten minute incubations, with the positive control serum adjusted to yield an absorbance of approximately 1.00. The results are reported as 'percentage of positive control' absorbance. The specificity of the reactions for thyroglobulin autoantibodies was supported by the good correlation found between the ELISA values obtained and the passive hemagglutination (PHA) titers of 348 sera from 333 patients suspected of having thyroid disturbances, as well as by antigen absorption experiments. Rheumatoid factor did not interfere with the assay. An appreciable proportion of passive hemagglutination-negative sera were confirmably positive for thyroglobulin autoantibodies by the ELISA method.
已开发出一种快速、特异、标准化、客观且灵敏的定量酶免疫测定法(ELISA),用于检测人甲状腺球蛋白自身抗体。该方法包括三次10分钟的温育,阳性对照血清经调整后吸光度约为1.00。结果以“阳性对照吸光度百分比”报告。在333例疑似甲状腺疾病患者的348份血清中,ELISA值与被动血凝(PHA)滴度之间存在良好相关性,以及抗原吸收实验均支持了甲状腺球蛋白自身抗体反应的特异性。类风湿因子不干扰该测定。通过ELISA法,相当一部分被动血凝阴性血清被确认为甲状腺球蛋白自身抗体阳性。