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恩济诺斯风疹检测:一种用于风疹病毒抗体筛查和定量的酶免疫测定法。

Enzygnost-Rubella: an enzyme immunoassay for screening and quantitation of antibodies to rubella virus.

作者信息

Madsen R D, Witheiler A P, Coates S R, Rippe D F

出版信息

Am J Clin Pathol. 1983 Feb;79(2):206-10. doi: 10.1093/ajcp/79.2.206.

Abstract

Calbiochem-Behring, Enzygnost-Rubella is an enzyme-linked immunosorbent assay (ELISA) for the determination of IgG antibodies to rubella virus. Two procedures, screening and quantitative, were used for the measurement of rubella antibodies in a characterized panel of sera and in random, premarital serum specimens. Using the screening procedure, no false-positive or false-negative results were observed in testing a panel of 40 sera previously characterized by human "O" cell and chick cell hemagglutination-inhibition (HI) tests. Additional testing of 323 random, premarital serum samples resulted in 99.4% agreement with HI tests in identifying positive and negative specimens. In the evaluation of the quantitative procedure, a coefficient of correlation (r) of 0.93 between ELISA titers and the geometric mean HI titers was obtained when testing the panel of 40 characterized sera. Furthermore, 100% agreement with HI test was obtained in the detection of titer rises in 20 pairs of acute and convalescent sera. The average within-run coefficients of variation for the screening and quantitative procedures were determined to be 11.2% and 15.6%, respectively. It is concluded that the Enzygnost-Rubella reagents are sensitive, specific, and provide objective means for assessing immunestatus and detecting rises in antibody titers to rubella virus.

摘要

Calbiochem - Behring公司的Enzygnost - 风疹检测是一种用于测定风疹病毒IgG抗体的酶联免疫吸附测定(ELISA)。采用筛查和定量两种方法对一组特征明确的血清以及随机抽取的婚前血清样本中的风疹抗体进行检测。使用筛查方法,在检测一组先前通过人“O”细胞和鸡胚细胞血凝抑制(HI)试验鉴定的40份血清时,未观察到假阳性或假阴性结果。对323份随机抽取的婚前血清样本进行的额外检测显示,在鉴定阳性和阴性样本方面,与HI试验的一致性达到99.4%。在评估定量方法时,对40份特征明确的血清样本进行检测时,ELISA滴度与几何平均HI滴度之间的相关系数(r)为0.93。此外,在检测20对急性和恢复期血清的滴度升高时,与HI试验的一致性达到100%。筛查和定量方法的批内变异系数平均值分别确定为11.2%和15.6%。结论是,Enzygnost - 风疹试剂灵敏、特异,为评估免疫状态和检测风疹病毒抗体滴度升高提供了客观手段。

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