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抗HIV检测试剂盒(IMx 8B32)的假阴性情况及其替代产品(IMx 8C98)的评估

False negativity by an anti-HIV assay kit (IMx 8B32) and evaluation of its replacement (IMx 8C98).

作者信息

Parry J V, Perry K R, Harbour S, Burgess C, Mortimer P P, Blackburn N K, Martin D

机构信息

Virus Reference Division, Central Public Health Laboratory, London, United Kingdom.

出版信息

J Med Virol. 1998 Oct;56(2):138-44.

PMID:9746070
Abstract

False negativity in a commercial anti-HIV kit (IMx HIV-1/HIV-2 3rd Generation Plus (code 8B32) was investigated, and the kit that superseded it (IMx HIV-1/HIV-2 III Plus, code 8C98) was evaluated. In a comparison on 574 freshly collected anti-HIV-1-positive specimens, 97.2% were more reactive in 8C98 than in 8B32; 35.5% were more than twice as reactive and 8.5% were more than four times as reactive. In 8B32, the signal from 55 specimens selected because of weak reactivity was enhanced 1.5 to 8.8 times by preliminary heating at 56 degrees C for 30 min. The reactivity of the 55 heated sera was then similar to that of the same specimens tested without heat treatment in the 8C98 assay. Reactivity in 8B32 was also increased in 66 of 76 (at least twofold in 20) randomly chosen anti-HIV-positive serum specimens by the addition of EDTA (10 mM final concentration). One of these specimens was false negative (signal:cutoff (S:CO) ratio 0.76) in 8B32, though its reactivity was restored by addition of EDTA (S:CO ratio 9.54). These findings indicate that the inhibitory effect that originally led to false negative findings in 8B32 was probably due to complement activity, and that the same activity was present in the freshly collected specimens used here to evaluate the replacement IMx anti-HIV assay (8C98). The specimen panel employed to evaluate 8C98 included 1,892 anti-HIV-positive and 779 anti-HIV-negative specimens. There were no false negative reactions. The lowest S:CO ratio observed was 6.2 and only 17 (0.2%) anti-HIV-positive specimens gave ratios less than 10. Nine unreproducible false positive reactions arose, all possibly attributable to specimen carryover by the IMx instrument. The performance of 8C98 was also compared with that of 10 other current anti-HIV kits using 21 sets of seroconversion specimens (127 specimens in total), and five performance assessment panels (92 specimens in total) comprised mostly of single bleeds from recent seroconverters. IMx 8C98 was the second most sensitive assay. We found no evidence that the 8C98 kit was prone to the effect that had given rise to false negative results in its predecessor (8B32).

摘要

对一款商用抗HIV试剂盒(IMx HIV-1/HIV-2第3代升级版(代码8B32))的假阴性情况进行了调查,并对其替代试剂盒(IMx HIV-1/HIV-2 III升级版,代码8C98)进行了评估。在对574份新采集的抗HIV-1阳性标本的比较中,97.2%的标本在8C98中的反应性高于8B32;35.5%的标本反应性高出两倍以上,8.5%的标本反应性高出四倍以上。在8B32中,因反应性较弱而挑选出的55份标本的信号,通过在56℃下初步加热30分钟,增强了1.5至8.8倍。然后,这55份加热血清的反应性与在8C98检测中未经热处理的相同标本的反应性相似。在76份随机选择的抗HIV阳性血清标本中,有66份通过添加EDTA(终浓度10 mM),8B32中的反应性也有所增加(20份至少增加了两倍)。其中一份标本在8B32中为假阴性(信号:临界值(S:CO)比值为0.76),不过添加EDTA后其反应性恢复(S:CO比值为9.54)。这些发现表明,最初导致8B32出现假阴性结果的抑制作用可能是由于补体活性,并且在此用于评估替代的IMx抗HIV检测(8C98)的新采集标本中也存在相同活性。用于评估8C98的标本组包括1892份抗HIV阳性标本和779份抗HIV阴性标本。未出现假阴性反应。观察到的最低S:CO比值为6.2,只有17份(0.2%)抗HIV阳性标本的比值小于10。出现了9次不可重复的假阳性反应,所有这些反应可能都归因于IMx仪器的标本残留。还使用21组血清转化标本(共127份标本)以及五个主要由近期血清转化者的单次出血组成的性能评估组(共92份标本),将8C98的性能与其他10种当前抗HIV试剂盒进行了比较。IMx 8C98是第二敏感的检测方法。我们没有发现证据表明8C98试剂盒容易出现导致其前身(8B32)出现假阴性结果的那种效应。

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