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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the Captia enzyme immunoassays for detection of immunoglobulins G and M to Treponema pallidum in syphilis.
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Evaluation of the Captia enzyme immunoassays for detection of immunoglobulins G and M to Treponema pallidum in syphilis.

机译:评估Captia酶免疫法对梅毒中梅毒螺旋体的免疫球蛋白G和M的检测。

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Two new enzyme-linked immunosorbent assays (ELISA), one for the measurement of immunoglobulin G (IgG) (Captia Syphilis-G) and one for the measurement of IgM (Captia Syphilis-M), were evaluated for detecting antibodies to Treponema pallidum. Serum samples from 169 patients, 96 with various stages of untreated syphilis, 63 with treated syphilis, and 10 who were noninfected, were investigated. All sera were also examined by traditional treponemal and cardiolipin tests and by the fluorescent treponemal antibody absorption (FTA-ABS) test for 19S(IgM). The overall sensitivity of Captia Syphilis-G was 98.3%. The IgG ELISA was very sensitive (100%) in all stages of untreated syphilis, except in primary syphilis (82%). In all diagnostic groups of syphilis, the reactivity of Captia Syphilis-M was similar to that of the 19S(IgM) FTA-ABS test, except in reinfections, in which the IgM capture ELISA was less sensitive. False-positive IgM capture ELISA results were not found in the 10 neonates born to mothers adequately treated for syphilis. However, of six serum samples containing rheumatoid factor, two were reactive in the Captia Syphilis-M test but not in the 19S(IgM) FTA-ABS test. This indicated that the specificity of the IgM capture ELISA was not absolute. All serum samples from treated patients were reactive in the IgG ELISA, but only 15 samples were reactive in the IgM capture ELISA, which appeared to be as effective as the 19S(IgM) FTA-ABS test in monitoring the effect of treatment. Simultaneous measurement of IgG and IgM antibodies for T. pallidum by the Captia immunoassays appears to be an efficient and simple method for confirming the diagnosis of syphilis as well as for indicating whether active disease is present.
机译:评估了两种新的酶联免疫吸附测定(ELISA),一种用于测定免疫球蛋白G(IgG)(梅毒-Captia Syphilis-G),另一种用于检测IgM(Captia Syphilis-M),用于检测抗梅毒螺旋体的抗体。研究了来自169例患者的血清样本,其中96例患有不同阶段的梅毒,63例患有梅毒,还有10例未感染。所有的血清也通过传统的色氨酸和心磷脂测试以及19S(IgM)的荧光色氨酸抗体吸收(FTA-ABS)测试进行了检查。 Captia Syphilis-G的总体敏感性为98.3%。 IgG ELISA在未经治疗的梅毒的所有阶段都非常敏感(100%),除了原发性梅毒(82%)。在梅毒的所有诊断组中,Captia Syphilis-M的反应性与19S(IgM)FTA-ABS测试相似,但在再感染中,IgM捕获ELISA的敏感性较低。在经过充分梅毒治疗的母亲所生的10例新生儿中,未发现IgM捕获呈假阳性。但是,在六个含有类风湿因子的血清样本中,有两个在Captia Syphilis-M测试中有反应,而在19S(IgM)FTA-ABS测试中则没有反应。这表明IgM捕获ELISA的特异性不是绝对的。来自接受治疗的患者的所有血清样品在IgG ELISA中均具有反应性,但在IgM捕获ELISA中仅具有反应性,在监测治疗效果方面似乎与19S(IgM)FTA-ABS测试一样有效。通过Captia免疫测定法同时测定苍白球菌IgG和IgM抗体,是确认梅毒诊断以及表明是否存在活动性疾病的有效而简单的方法。

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