首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Enzyme-linked immunosorbent assay for detection of respiratory syncytial virus infection: application to clinical samples.
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Enzyme-linked immunosorbent assay for detection of respiratory syncytial virus infection: application to clinical samples.

机译:酶联免疫吸附法检测呼吸道合胞病毒感染:应用于临床样品。

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摘要

An enzyme-linked immunosorbent assay (ELISA) for respiratory syncytial virus antigens was applied to the rapid diagnosis of acute infections in children and was compared with viral culture and immunofluorescence tests. The ELISA test employed commercially available reagents and was run on a day-to-day basis as specimens were received in the laboratory. Sensitivity and specificity by ELISA were 82 and 95%, respectively, compared with culture. In the same specimens, the sensitivity and specificity by immunofluorescence were 86 and 96%, respectively. Nasopharyngeal aspirates were proven to be a better source of viral antigen than were nasopharyngeal swabs. ELISA-positive samples remained positive even when left unrefrigerated for a week or mailed to the laboratory in plastic containers. Respiratory syncytial virus ELISA, like culture, became negative as the disease progressed and showed no superiority over culture for diagnosis late in the illness.
机译:呼吸道合胞病毒抗原的酶联免疫吸附试验(ELISA)用于儿童急性感染的快速诊断,并与病毒培养和免疫荧光试验进行了比较。 ELISA测试采用市售试剂,并且在实验室接收标本的情况下每天进行。与培养相比,ELISA的灵敏度和特异性分别为82%和95%。在同一样本中,免疫荧光的敏感性和特异性分别为86%和96%。事实证明,鼻咽抽吸物比鼻咽拭子是一种更好的病毒抗原来源。即使未冷藏一周或用塑料容器邮寄到实验室,ELISA阳性样品仍保持阳性。呼吸道合胞病毒酶联免疫吸附测定(ELISA)与培养物一样,随着疾病的发展而呈阴性,并且在疾病后期诊断中没有优于培养物。

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