Kishimoto T, Kubota Y, Matsushima T, Izutsu H, Matsumoto A, Soejima R, Morikawa T, Kawagoe K
Department of Internal Medicine, Kawasaki Medical School.
Kansenshogaku Zasshi. 1996 Aug;70(8):821-9. doi: 10.11150/kansenshogakuzasshi1970.70.821.
Studies were conducted with the goal of developing a kit for assaying anti-Chlamydia pneumoniae antibodies in human serum which would enable judging positive cases with high specificity by means of an objective numerical index. Thus, an enzyme-linked immunosorbent assay (ELISA) method employing a C. pneumoniae outer membrane complex protein was established. Elementary bodies (EB) were purified from the YK-41 strain of C. pneumoniae, and subsequent treatment with Sarkosyl, DNase and RNase yielded chlamydial outer membrane complex (COMC). COMC was employed as the antigen and immobilized on 96-well microplates for ELISA method. This ELISA method was used to test 51 serum specimens from patients who had been demonstrated to be positive for C. pneumoniae antigen (throat swab: PCR positive), and the levels of IgG, IgA and IgM antibodies were assayed. For each specimen, comparison was made with the antibody titers determined by the micro immunofluorescence test (Micro-IF method). The results showed good correlation coefficients of 0.950 for IgG, 0.852 for IgA and 0.866 for IgM. In addition, the two assay methods showed the following high agreement rates: 90.2% for IgG, 84.3% for IgA and 82.4% for IgM. Specimens which did not yield the same results with the ELISA method and Micro-IF method were subjected to analysis by Western blot method, and the rates of agreement with the ELISA results were 80% for IgG, 87.5% for IgA and 88.9% for IgM. These data indicate the efficacy of this new ELISA method. Moreover, COMC was reacted with mouse antisera to three Chlamydia species, and the mouse IgG antibody was assayed. Anti-C. pneumoniae antiserum showed the strongest reactivity, whereas weaker reactivity was shown by anti-C. trachomatis antiserum (1/32nd of the reactivity of the anti-C. pneumoniae antiserum) and anti-C. psittaci antiserum (1/4th). In addition, sera from patients infected with C. trachomatis or C. psittaci (Psittacosis) were subjected to the ELISA method using COMC from C. pneumoniae. It was found that the correlation between the ELISA and Micro-IF methods was higher in relation to the anti-C. pneumoniae antibody titer than either the anti-C. trachomatis antibody titer or anti-C. psittaci antibody titer. These findings indicate this new assay kit based on the ELISA method has high specificity for C. pneumoniae.
开展了多项研究,目的是开发一种用于检测人血清中抗肺炎衣原体抗体的试剂盒,该试剂盒能够通过客观的数值指标高特异性地判断阳性病例。因此,建立了一种采用肺炎衣原体外膜复合蛋白的酶联免疫吸附测定(ELISA)方法。从肺炎衣原体YK - 41菌株中纯化出原体(EB),随后用十二烷基肌氨酸钠、DNA酶和RNA酶处理得到衣原体外膜复合物(COMC)。将COMC用作抗原并固定在96孔微孔板上用于ELISA方法。该ELISA方法用于检测51份已被证明肺炎衣原体抗原阳性(咽拭子:PCR阳性)患者的血清标本,并测定IgG、IgA和IgM抗体水平。对于每份标本,将其与通过微量免疫荧光试验(微量IF法)测定的抗体滴度进行比较。结果显示,IgG的相关系数为0.950,IgA为0.852,IgM为0.866,相关性良好。此外,两种检测方法显示出以下高一致率:IgG为90.2%,IgA为84.3%,IgM为82.4%。ELISA方法和微量IF法结果不同的标本采用蛋白质印迹法进行分析,与ELISA结果的一致率分别为:IgG为80%,IgA为87.5%,IgM为88.9%。这些数据表明这种新的ELISA方法有效。此外,使COMC与针对三种衣原体的小鼠抗血清反应,并测定小鼠IgG抗体。抗肺炎衣原体抗血清显示出最强的反应性,而抗沙眼衣原体抗血清的反应性较弱(为抗肺炎衣原体抗血清反应性的1/32),抗鹦鹉热衣原体抗血清的反应性较弱(为1/4)。此外,使用肺炎衣原体的COMC对感染沙眼衣原体或鹦鹉热衣原体(鹦鹉热)患者的血清进行ELISA方法检测。结果发现,ELISA方法与微量IF法之间,针对抗肺炎衣原体抗体滴度的相关性高于抗沙眼衣原体抗体滴度或抗鹦鹉热衣原体抗体滴度。这些发现表明这种基于ELISA方法的新检测试剂盒对肺炎衣原体具有高特异性。