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首页> 外文期刊>Journal of Clinical Microbiology >Standardization of Immunoglobulin M Capture Enzyme-Linked Immunosorbent Assays for Routine Diagnosis of Arboviral Infections
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Standardization of Immunoglobulin M Capture Enzyme-Linked Immunosorbent Assays for Routine Diagnosis of Arboviral Infections

机译:虫卵病毒感染常规诊断的免疫球蛋白M捕获酶联免疫吸附测定的标准化

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摘要

Immunoglobulin M antibody-capture enzyme-linked immunosorbent assay (MAC-ELISA) is a rapid and versatile diagnostic method that readily permits the combination of multiple assays. Test consolidation is especially important for arthropod-borne viruses (arboviruses) which belong to at least three virus families: the Togaviridae,Flaviviridae, and Bunyaviridae. Using prototype viruses from each of these families and a panel of well-characterized human sera, we have evaluated and standardized a combined MAC-ELISA capable of identifying virus infections caused by members of each virus family. Furthermore, by grouping antigens geographically and utilizing known serological cross-reactivities, we have reduced the number of antigens necessary for testing, while maintaining adequate detection sensitivity. We have determined that a 1:400 serum dilution is most appropriate for screening antiviral antibody, using a positive-to-negative ratio of ≥2.0 as a positive cutoff value. With a blind-coded human serum panel, this combined MAC-ELISA was shown to have test sensitivity and specificity that correlated well with those of other serological techniques.
机译:免疫球蛋白M抗体捕获酶联免疫吸附测定(MAC-ELISA)是一种快速且通用的诊断方法,可轻松实现多种测定的组合。测试整合对于节肢动物传播的病毒(虫媒病毒)尤其重要,该病毒至少属于三个病毒家族: Togaviridae Flaviviridae Bunyaviridae 。使用来自这些家族中的每个家族的原型病毒和一组特征明确的人类血清,我们评估并标准化了一种能够识别由每个病毒家族成员引起的病毒感染的组合MAC-ELISA。此外,通过在地理上对抗原进行分组并利用已知的血清学交叉反应性,我们在保持足够的检测灵敏度的同时,减少了测试所需的抗原数量。我们已经确定,使用正负比(≥2.0)作为正截止值时,以1:400的血清稀释度最适合筛选抗病毒抗体。使用盲法编码的人血清检测试剂盒,表明该组合的MAC-ELISA具有与其他血清学技术良好的相关性。

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