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Standardization of enzyme-linked immunosorbent assay ELISA to detect anti-Toxoplasma gondii IgM and IgG antibodies, and comparison with the indirect immunofluorescence technique

机译:酶联免疫吸附测定ELISA的标准方法,用于检测弓形虫抗IgM和IgG抗体,并与间接免疫荧光技术进行比较

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s Serology has been the most popular method to diagnose toxoplasmosis. Accordingly, this study standardizes an enzyme-linked immunosorbent assay (ELISA) and compares its results with the IFI technique. In the IgG detection test, the standardized technique presented a sensibility (S) of 96.77%, a specificity (SP) of 75%, with a positive predictive value (PPV) of 83.33%, a negative predictive value (NPV) of 94.74%, and an adjusted concordance (K) of 73.50%. The IFI exhibited 83.87% for S, 79.16% for SP, 83.81% for PPV, 79.16% for NPV, and 63% for K. The rough concordance between these two tests (ELISA/IFI) was 88.35% for the IgG detection test and 81.55% for the IgM detection test. K was 70.82% and 1.31% for IgG and IgM, respectively, the correlation index (r) being 0.556 for IgG and -0.023 for IgM. We can conclude that standardized ELISA-IgG is indicated in serologic selection processes, whereas the ELISA-IgM is not recommended for presenting low values for the adjusted concordance with the reference technique, which suggests not very reliable results.
机译:血清学一直是诊断弓形虫病的最流行方法。因此,本研究对酶联免疫吸附测定(ELISA)进行了标准化,并将其结果与IFI技术进行了比较。在IgG检测测试中,标准化技术的灵敏度(S)为96.77%,特异性(SP)为75%,阳性预测值(PPV)为83.33%,阴性预测值(NPV)为94.74% ,调整后的一致性(K)为73.50%。 IFI表现出S的83.87%,SP的79.16%,PPV的83.81%,NPV的79.16%和K的63%。这两个测试(ELISA / IFI)的IgG检验和IgM检测测试为81.55%。 IgG和IgM的K分别为70.82%和1.31%,相关指数(r)对于IgG为0.556,对于IgM为-0.023。我们可以得出结论,血清学选择过程中需要标明标准化的ELISA-IgG,而不建议使用ELISA-IgM来提供与参考技术一致的低值,这表明结果不是很可靠。

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