A simple ELISA capable of distinguishing between IgG antibodies to Chlamydia trachomatis and Chlamydia pneumoniae

Maureen G. Friedman , Shlomo Ilan , Simona Kahane , Nani Kosashvili , Yona Bir , David Lieberman
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引用次数: 3

Abstract

Simple assays which reliably distinguish between past infection with Chlamydia pneumoniae and with Chlamydia trachomatis are needed. We developed an enzyme-linked immunosorbent assay (ELISA) for this purpose by reducing antigen cross reactive lipopolysaccharide epitopes with deoxycholate treatment and releasing antibodies of low affinity with a 6 M urea wash step. Paired serum samples from 212 patients with non-C. pneumoniae-associated community acquired pneumonia and single serum samples from 61 healthy students, 61 women with gynaecological complaints, and 100 blood donors were tested in the assay system. Excellent positive/negative correlation with the microimmunofluorescence (MIF) test was shown. This urea ELISA assay may be useful in assessment of past infection with these organisms, especially in epidemiological studies.

一个简单的ELISA能够区分沙眼衣原体和肺炎衣原体的IgG抗体
需要简单的测定方法来可靠地区分过去感染的肺炎衣原体和沙眼衣原体。为此,我们开发了一种酶联免疫吸附试验(ELISA),通过脱氧胆酸处理减少抗原交叉反应性脂多糖表位,并通过6米尿素洗涤步骤释放低亲和力的抗体。对212例非丙型肝炎患者的血清样本进行配对。对61名健康学生、61名妇科疾患妇女和100名献血者的肺炎相关社区获得性肺炎和单血清样本进行检测。与微免疫荧光(MIF)试验呈极好的正/负相关。尿素酶联免疫吸附试验可用于评估过去感染这些微生物,特别是在流行病学研究中。
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