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急性盆腔炎患者对沙眼衣原体的抗原特异性血清抗体反应。

Antigen specific serum antibody response to Chlamydia trachomatis in patients with acute pelvic inflammatory disease.

作者信息

Miettinen A, Heinonen P K, Teisala K, Punnonen R, Paavonen J

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

J Clin Pathol. 1990 Sep;43(9):758-61. doi: 10.1136/jcp.43.9.758.

Abstract

Sera from 35 patients with acute pelvic inflammatory disease (PID) with and without Chlamydia trachomatis confirmed by culture and sera from 19 control patients with neither evidence of pelvic infection nor C trachomatis infection were studied for the presence of serum IgG, IgA, and IgM antibodies to C trachomatis using enzyme immunoassay (EIA) and immunoblotting techniques. There was no correlation between the antibody concentrations in the EIA and the spread of chlamydial infection, as determined by cervical, endometrial, and laparoscopic sampling for chlamydia. The immunoblot analysis showed antibodies to the major outer membrane protein (MOMP) of C trachomatis elementary bodies in all patients who had had C trachomatis isolated. Reactivity was also frequently observed against the 68, 62, 60, 45, and 31 kilodalton antigens. About 20 antigenic polypeptides were identified. Differences in antibody prevalence to specific chlamydial antigens, however, were not related to the site of chlamydial isolation or serum antibody concentrations observed with the EIA. The results indicate that patients with PID with and without upper genital tract infection with C trachomatis cannot be differentiated by reactivity of sera to specific chlamydial polypeptide antigens. The determination of a specific serum IgA antibody response by EIA was the most effective single test to discriminate between patients with and without acute chlamydial infection.

摘要

对35例经培养确诊有或无沙眼衣原体感染的急性盆腔炎(PID)患者的血清,以及19例既无盆腔感染迹象也无沙眼衣原体感染的对照患者的血清,采用酶免疫测定(EIA)和免疫印迹技术研究针对沙眼衣原体的血清IgG、IgA和IgM抗体的存在情况。通过对宫颈、子宫内膜和腹腔镜取样检测衣原体来确定,EIA中的抗体浓度与衣原体感染的传播之间没有相关性。免疫印迹分析显示,所有分离出沙眼衣原体的患者体内都有针对沙眼衣原体原体主要外膜蛋白(MOMP)的抗体。还经常观察到对68、62、60、45和31千道尔顿抗原的反应性。大约鉴定出20种抗原多肽。然而,针对特定衣原体抗原的抗体流行率差异与衣原体分离部位或EIA观察到的血清抗体浓度无关。结果表明,无论有无沙眼衣原体上生殖道感染的PID患者,不能通过血清对特定衣原体多肽抗原的反应性来区分。通过EIA测定特异性血清IgA抗体反应是区分有无急性衣原体感染患者的最有效的单项检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1d/502756/7402f08f68ad/jclinpath00399-0060-a.jpg

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