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用于虫媒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

Standardization of immunoglobulin M capture enzyme-linked immunosorbent assays for routine diagnosis of arboviral infections.

作者信息

Martin D A, Muth D A, Brown T, Johnson A J, Karabatsos N, Roehrig J T

机构信息

Division of Vector-Borne Infectious Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Fort Collins, Colorado 80522, USA.

出版信息

J Clin Microbiol. 2000 May;38(5):1823-6. doi: 10.1128/JCM.38.5.1823-1826.2000.

DOI:10.1128/JCM.38.5.1823-1826.2000
PMID:10790107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC86599/
Abstract

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.

摘要

免疫球蛋白M抗体捕获酶联免疫吸附测定法(MAC-ELISA)是一种快速且通用的诊断方法,很容易实现多种检测的组合。检测整合对于节肢动物传播病毒(虫媒病毒)尤为重要,这些病毒至少属于三个病毒科:披膜病毒科、黄病毒科和布尼亚病毒科。利用来自这些病毒科的原型病毒和一组特征明确的人血清,我们评估并标准化了一种联合MAC-ELISA,它能够识别由每个病毒科成员引起的病毒感染。此外,通过按地理位置对抗原进行分组并利用已知的血清学交叉反应性,我们减少了检测所需的抗原数量,同时保持了足够的检测灵敏度。我们确定,使用阳性与阴性比值≥2.0作为阳性临界值时,1:400的血清稀释度最适合用于筛选抗病毒抗体。对于一组盲编码的人血清,这种联合MAC-ELISA的检测灵敏度和特异性与其他血清学技术的灵敏度和特异性具有良好的相关性。