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用于检测抗1型和2型人类免疫缺陷病毒抗体的新型双抗原夹心酶免疫测定法的多中心评估

Multicenter evaluation of new double-antigen sandwich enzyme immunoassay for measurement of anti-human immunodeficiency virus type 1 and type 2 antibodies.

作者信息

Burgisser P, Simon F, Wernli M, Wust T, Beya M F, Frei P C

机构信息

Division d'Immunologie et Allergie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

出版信息

J Clin Microbiol. 1996 Mar;34(3):634-7. doi: 10.1128/jcm.34.3.634-637.1996.

Abstract

A new enzyme immunoassay (EIA), the Cobas Core Anti-HIV-1/HIV-2 EIA DAGS (also referred to as Roche DAGS), for the detection of antibodies to human immunodeficiency virus type 1 (HIV-1) and HIV-2 was evaluated in four centers. The assay is based on the double-antigen sandwich (DAGS) format, which enables the detection of all classes of antibodies. The antigens consist of recombinant proteins in their native conformation and of synthetic peptides. Of a total of 5,836 negative serum samples, including 95 samples likely to produce false reactivities, 6 were false positive, resulting in a specificity of 99.9%. None of 35 sera that were from noninfected individuals but contained p24-cross-reacting antibodies as revealed by Western blot (immunoblot) analysis were reactive by the Roche DAGS assay. In samples from individuals infected with HIV-1 group M (n = 499) and HIV-2 (n = 200), the sensitivity of the assay was 100%. Although containing antigens with sequences from subtype B only, the assay was also able to correctly identify with high optical density/cutoff ratios samples from subjects infected with HIV-1 subtype O (n = 10). In 17 of 19 seroconversion panels tested, the assay detected the presence of HIV-1 antibodies as early as another sandwich EIA. Eight of these panels were also analyzed by an indirect second-generation assay, which detected antibodies 2 to 10 days later than did the DAGS assay under evaluation. The excellent specificity and sensitivity of the new Cobas Core Anti-HIV-1/HIV-2 EIA DAGS are the result of the DAGS format as well as of the native, naturally folded form of the recombinant protein used as the gag antigen.

摘要

一种用于检测人免疫缺陷病毒1型(HIV-1)和HIV-2抗体的新型酶免疫测定法(EIA)—— cobas Core Anti-HIV-1/HIV-2 EIA DAGS(也称为罗氏DAGS),在四个中心进行了评估。该测定法基于双抗原夹心(DAGS)形式,能够检测所有类别的抗体。抗原由天然构象的重组蛋白和合成肽组成。在总共5836份阴性血清样本中,包括95份可能产生假反应性的样本,有6份为假阳性,特异性为99.9%。通过蛋白质印迹(免疫印迹)分析显示,35份来自未感染个体但含有p24交叉反应抗体的血清,用罗氏DAGS测定法均无反应性。在感染HIV-1 M组(n = 499)和HIV-2(n = 200)个体的样本中,该测定法的灵敏度为100%。尽管该测定法仅含有B亚型序列的抗原,但也能够以高光学密度/临界值比值正确鉴定来自感染HIV-1 O亚型(n = 10)受试者的样本。在测试的19个血清转化样本组中的17个中,该测定法与另一种夹心EIA一样,能够尽早检测到HIV-1抗体的存在。其中8个样本组还通过间接第二代测定法进行了分析,该方法检测抗体的时间比正在评估的DAGS测定法晚2至10天。新型cobas Core Anti-HIV-1/HIV-2 EIA DAGS的优异特异性和灵敏度是DAGS形式以及用作gag抗原的重组蛋白的天然、自然折叠形式的结果。

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