Burgisser P, Simon F, Wernli M, Wust T, Beya M F, Frei P C
Division d'Immunologie et Allergie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
J Clin Microbiol. 1996 Mar;34(3):634-7. doi: 10.1128/jcm.34.3.634-637.1996.
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.
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。