Saikku P, Paavonen J, Väänänen P, Vaheri A
J Clin Microbiol. 1983 Jan;17(1):22-7. doi: 10.1128/jcm.17.1.22-27.1983.
An enzyme immunoassay (EIA) for chlamydial immunoglobulin G antibodies was developed by using microtiter wells coated with partially purified reticulate bodies of Chlamydia trachomatis serotype L2, grown in McCoy cells, and uninfected McCoy cells as a control. Duplicate testing of a single serum dilution, 1:500, was found to be sufficient. A good correlation between positive reactions was observed in a comparative study of 421 patient sera with the EIA and an inclusion immunofluorescence test. A good correlation between positive reactions was also observed in a comparative study of 140 patient sera with EIA and microimmunofluorescence tests in which chlamydial elementary or reticulate bodies were used as antigens. Sera of 77 healthy control individuals with low titers in inclusion immunofluorescence or complement fixation tests gave negative results in the EIA. Immunoblotting experiments showed that the major antigenic component in the EIA antigen was a protein with an Mr of 39,000.
通过使用包被有沙眼衣原体L2血清型部分纯化的网状体的微量滴定板来开发一种用于衣原体免疫球蛋白G抗体的酶免疫测定法(EIA),该网状体在McCoy细胞中生长,并使用未感染的McCoy细胞作为对照。发现对单一血清稀释度(1:500)进行重复检测就足够了。在一项对421份患者血清进行的EIA与包涵体免疫荧光试验的比较研究中,观察到阳性反应之间有良好的相关性。在一项对140份患者血清进行的EIA与微量免疫荧光试验的比较研究中也观察到阳性反应之间有良好的相关性,其中使用衣原体原体或网状体作为抗原。77名在包涵体免疫荧光或补体结合试验中滴度较低的健康对照个体的血清在EIA中呈阴性结果。免疫印迹实验表明,EIA抗原中的主要抗原成分是一种分子量为39,000的蛋白质。