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首页> 外文期刊>Journal of Clinical Microbiology >Comparison of five commercial enzyme-linked immunosorbent assays and Western immunoblotting for human immunodeficiency virus antibody detection in serum samples from Central Africa.
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Comparison of five commercial enzyme-linked immunosorbent assays and Western immunoblotting for human immunodeficiency virus antibody detection in serum samples from Central Africa.

机译:比较五种商业酶联免疫吸附测定法和Western免疫印迹法对中非血清样品中人免疫缺陷病毒抗体的检测。

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Detection by five different enzyme-linked immunosorbent assays (ELISAs) of antibody to human immunodeficiency virus (HIV) in sera from three Zairian populations consisting of 1,998 individuals with various risks for HIV infection was evaluated. Sera that were reactive by at least one assay and 10% of the nonreactive serum samples were analyzed by Western blot (immunoblot) by using U.S. Public Health Service interpretation criteria. Sera which were positive by ELISA for detection of antibody to HIV-1 and HIV-2 and negative or indeterminate by HIV-1 Western blot were also analyzed by HIV-2 Western blot. Overall, 443 (22.2%) serum specimens were HIV-1 Western blot positive, 390 (19.5%) had indeterminate HIV-1 Western blot patterns, and no samples were HIV-2 Western blot positive. The sensitivity of the ELISAs ranged from 97.5 to 99.8%, and the specificity ranged from 51.7 to 98.4%. By population group, the negative predictive value ranged from 97.1 to 100%, in contrast to the positive predictive value, which varied from 6.6 to 100%. Follow-up results for sera which were indeterminate for antibody to HIV-1 documented only four seroconversions (6.0%) among 67 individuals at high risk for HIV-1 infection and no seroconversions among 202 individuals at relatively low risk for HIV-1 infection. This study demonstrates the importance of evaluating commercial ELISAs with sera from appropriate geographical regions in order to select the most cost-effective and practical assay for use in that region. Furthermore, the high frequency of indeterminate Western blots for African sera emphasizes the continual need for improved confirmatory assays and interpretation criteria.
机译:通过五种不同的酶联免疫吸附测定(ELISA),检测了来自三个扎伊尔人群的血清中针对人类免疫缺陷病毒(HIV)的抗体,该人群包括1,998名具有各种HIV感染风险的个体。使用美国公共卫生服务局的解释标准,通过Western印迹(免疫印迹)分析了至少一种测定具有反应性的血清和10%的非反应性血清样品。还通过HIV-2 Western印迹分析了用于检测针对HIV-1和HIV-2的抗体的ELISA阳性的血清以及通过HIV-1 Western印迹检测的阴性或不确定的血清。总体而言,有443个(22.2%)血清标本为HIV-1 Western blot阳性,有390个(19.5%)具有不确定的HIV-1 Western blot模式,没有样品为HIV-2 Western blot阳性。 ELISA的灵敏度范围为97.5至99.8%,特异性范围为51.7至98.4%。按人群划分,阴性预测值为97.1至100%,而阳性预测值为6.6至100%。对HIV-1抗体不确定的血清随访结果表明,在67位HIV-1高感染风险人群中只有4次血清转化(6.0%),而在HIV-1感染风险相对较低的202个人中没有血清转化。这项研究表明,评估来自适当地理区域血清的商业ELISA的重要性,以便选择在该区域使用的最具成本效益和最实用的检测方法。此外,用于非洲血清的不确定性Western印迹的高频率强调了不断需要改进的确证测定和解释标准。

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