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首页> 外文期刊>Journal of Clinical Microbiology >Enzyme immunoassay for measurement of antibodies to herpes simplex virus infection: comparison with complement fixation, immunofluorescent-antibody, and neutralization techniques.
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Enzyme immunoassay for measurement of antibodies to herpes simplex virus infection: comparison with complement fixation, immunofluorescent-antibody, and neutralization techniques.

机译:用于测量单纯疱疹病毒感染抗体的酶免疫测定:与补体固定,免疫荧光抗体和中和技术的比较。

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An enzyme immunoassay (EIA) was developed for detecting antibody to herpes simplex virus, and the results were compared with those of complement fixation, indirect immunofluorescent-antibody, and plaque reduction neutralization tests. Test sera showed very little nonspecific reactivity even at a starting dilution as low as 1:10. EIA results showed excellent correlation with results obtained by the neutralization test, with an average gain in sensitivity of 1.65. EIA proved very useful in detecting current herpes simplex virus infection, and antibody appeared in all cases soon after clinical onset. EIA appears to be a rapid, sensitive, and specific method for routine demonstration of herpes simplex virus antibody in a clinical setting.
机译:开发了用于检测单纯疱疹病毒抗体的酶免疫法(EIA),并将结果与​​补体固定法,间接免疫荧光抗体法和噬菌斑减少中和法进行了比较。测试血清显示出极低的非特异性反应性,即使在起始稀释度低至1:10时也是如此。 EIA结果显示与中和试验获得的结果具有极好的相关性,灵敏度平均提高1.65。 EIA被证明对检测当前的单纯疱疹病毒感染非常有用,并且在临床发病后不久所有病例均出现抗体。 EIA似乎是一种在临床环境中常规证明单纯疱疹病毒抗体的快速,灵敏和特异的方法。

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