Bachmann P, Beyer J, Brust S, Engelhardt W, Gürtler L G, Habermehl K O, Karakassopoulos A, Michl U, Mühlbacher A, Stöffler-Meilicke M
Swiss Red Cross, Central Laboratory, Bern, Switzerland.
Infection. 1995 Sep-Oct;23(5):322-33. doi: 10.1007/BF01716301.
The aim of the study was to evaluate a new ELISA for detection of HIV-1, HIV-2 and HIV-1 subtype 0 (HIV-0) antibodies. The assay format is based on the antigen sandwich principle. To enable specific detection of HIV-0 antibodies, in addition to HIV-1 and HIV-2 antigens HIV-0 antigen is used for coating the solid phase and for the conjugate. The results show that all 12 HIV-0 samples tested were detected with a high degree of reactivity, as were all the 1,144 anti-HIV-1 and 424 anti-HIV-2 positive samples. The capacity of the test to enable early detection of seroconversions is equivalent to that of other sandwich ELISAs. The specificity of the assay was determined to be 99.89/99.94% (initial/after retest) using 58,366 samples, which is superior to the other ELISAs used for comparison. Even with difficult samples (i.e. samples of African origin, samples known to cause false-positive reactivity in different ELISAs, or samples containing potential interference factors) there were very few false-positive reactions. Therefore, the new assay is well suited for screening blood donations as well as for evaluating samples from patients of different geographic origin.
该研究的目的是评估一种用于检测HIV-1、HIV-2和HIV-1 0亚型(HIV-0)抗体的新型酶联免疫吸附测定(ELISA)。该检测方法基于抗原夹心原理。为了能够特异性检测HIV-0抗体,除了HIV-1和HIV-2抗原外,HIV-0抗原还用于包被固相和用于缀合物。结果显示,所有检测的12份HIV-0样本均具有高度反应性,所有1144份抗HIV-1阳性样本和424份抗HIV-2阳性样本也是如此。该检测方法早期检测血清转化的能力与其他夹心ELISA相当。使用58366份样本确定该检测方法的特异性为99.89/99.94%(初次检测/复测后),优于用于比较的其他ELISA。即使对于困难样本(即非洲来源的样本、已知在不同ELISA中会引起假阳性反应的样本或含有潜在干扰因素的样本),假阳性反应也非常少。因此,这种新检测方法非常适合用于筛查献血以及评估来自不同地理区域患者的样本。