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生殖道感染中的衣原体血清学检测:免疫组合法与伊帕齐姆法的比较

Chlamydial serology in genital infections: ImmunoComb versus Ipazyme.

作者信息

Clad A, Flecken U, Petersen E E

机构信息

Universitäts-Frauenklinik, Freiburg, Germany.

出版信息

Infection. 1993 Nov-Dec;21(6):384-9. doi: 10.1007/BF01728919.

Abstract

The ImmunoComb Chlamydia trachomatis IgG/IgA (Orgenics, Israel) is a new serologic test using C. trachomatis L2 elementary bodies (Washington Research Foundation, Seattle) as antigen. The Ipazyme IgG/IgA test (Savyon, Israel) employs whole cells with C. trachomatis L2 inclusions, i.e. elementary and reticulate bodies. Theoretically, the ImmunoComb is expected to be less cross-reactive (LPS) with Chlamydia pneumoniae than the Ipazyme (LPS and reticulate body group specific antigens). Compared with the Ipazyme, the ImmunoComb IgA showed both a higher positive predictive value (36% versus 25%) and sensitivity (67% versus 33%) for antigen detection in a control group of 100 post partum women with a 6% prevalence of C. trachomatis positive cervical smears. In sterility patients (45 cases with occluded and 53 with open fallopian tubes) the tube status was predicted by the ImmunoComb (Ipazyme) with 74% (72%) positive predictive value, 87% (80%) sensitivity, and 87% (81%) negative predictive value. IgG/IgA prevalence in 118 patients with C. trachomatis positive cervical smears was 85%/55% for the ImmunoComb and 84%/49% for the Ipazyme. The ImmunoComb is considerably faster and easier in handling and less subjective in reading than the Ipazyme.

摘要

免疫组合沙眼衣原体IgG/IgA检测试剂盒(以色列奥根尼克斯公司)是一种新型血清学检测方法,它使用沙眼衣原体L2原体(华盛顿研究基金会,西雅图)作为抗原。伊帕酶IgG/IgA检测试剂盒(以色列萨维昂公司)采用含有沙眼衣原体L2包涵体的全细胞,即原体和网状体。从理论上讲,预计免疫组合检测试剂盒与肺炎衣原体的交叉反应性(脂多糖)低于伊帕酶检测试剂盒(脂多糖和网状体组特异性抗原)。在100名沙眼衣原体宫颈涂片阳性患病率为6%的产后妇女对照组中,与伊帕酶检测试剂盒相比,免疫组合IgA检测试剂盒在抗原检测方面具有更高的阳性预测值(分别为36%和25%)和敏感性(分别为67%和33%)。在不育患者中(45例输卵管堵塞,53例输卵管通畅),免疫组合检测试剂盒(伊帕酶检测试剂盒)对输卵管状况的预测阳性预测值为74%(72%),敏感性为87%(80%),阴性预测值为87%(81%)。在118例沙眼衣原体宫颈涂片阳性患者中,免疫组合检测试剂盒的IgG/IgA患病率为85%/55%,伊帕酶检测试剂盒为84%/49%。与伊帕酶检测试剂盒相比,免疫组合检测试剂盒操作起来要快得多、容易得多,且判读时主观性更小。

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