Kiviat N B, Wølner-Hanssen P, Peterson M, Wasserheit J, Stamm W E, Eschenbach D A, Paavonen J, Lingenfelter J, Bell T, Zabriskie V
Am J Obstet Gynecol. 1986 Apr;154(4):865-73. doi: 10.1016/0002-9378(86)90473-4.
Fifty-five women with suspected pelvic inflammatory disease underwent diagnostic laparoscopy and endometrial and tubal biopsy, with specimens for isolation of Chlamydia trachomatis and for staining with a species-specific monoclonal fluorescein-conjugated antibody to C. trachomatis were obtained from the urethra, rectum, endocervix, endometrium, tubes, and cul-de-sac. C. trachomatis was isolated from 21 patients (38%), including 10 (18%) who had positive endometrial or tubal cultures. The fluorescein-conjugated antibody stain was positive for 43 (86%) of 50 culture-positive specimens, for 14 (18%) of 78 culture-negative specimens from 21 patients who had positive cultures from other sites, and for one (0.5%) of 192 specimens from 34 patients who had negative cultures at all sites. Thus the sensitivity of direct fluorescein-conjugated antibody for culture-positive specimens was 86% and the specificity for specimens from culture-negative patients was 99%. Twelve upper genital tract specimens were positive by fluorescein-conjugated antibody only. Fluorescein-conjugated antibody staining of 50 paraffin-embedded endometrial aspirates showed extracellular or intracellular elementary bodies and or cytoplasmic inclusions in all of seven culture-positive specimens, in four of six culture-negative specimens from patients who had positive cultures at other sites, and in none of 34 specimens from patients with negative cultures. Thus fluorescein-conjugated antibody staining is useful for confirming the role of C. trachomatis in endometritis and salpingitis. It is more sensitive than culture for detection of chlamydia in endometrial or tubal specimens and is able to confirm that the organism is actually present in endometrial tissue (rather than simply reflecting contamination from the cervix) in women with clinical evidence of pelvic inflammatory disease.
55名疑似盆腔炎的女性接受了诊断性腹腔镜检查以及子宫内膜和输卵管活检,从尿道、直肠、宫颈管内膜、子宫内膜、输卵管和直肠子宫陷凹获取标本,用于分离沙眼衣原体以及用针对沙眼衣原体的种特异性单克隆荧光素结合抗体进行染色。21名患者(38%)分离出沙眼衣原体,其中10名(18%)子宫内膜或输卵管培养阳性。50份培养阳性标本中有43份(86%)荧光素结合抗体染色呈阳性,来自21名其他部位培养阳性患者的78份培养阴性标本中有14份(18%)呈阳性,来自34名所有部位培养均为阴性患者的192份标本中有1份(0.5%)呈阳性。因此,直接荧光素结合抗体对培养阳性标本的敏感性为86%,对培养阴性患者标本的特异性为99%。12份上生殖道标本仅荧光素结合抗体呈阳性。对50份石蜡包埋的子宫内膜吸出物进行荧光素结合抗体染色,结果显示,7份培养阳性标本全部可见细胞外或细胞内原体和/或细胞质包涵体,来自其他部位培养阳性患者的6份培养阴性标本中有4份可见,而34份培养阴性患者的标本均未见到。因此,荧光素结合抗体染色有助于确认沙眼衣原体在子宫内膜炎和输卵管炎中的作用。在检测子宫内膜或输卵管标本中的衣原体时,它比培养更敏感,并且能够证实盆腔炎临床证据的女性子宫内膜组织中确实存在该病原体(而不是简单地反映来自宫颈的污染)。