Dawson G J, Heller J S, Wood C A, Gutierrez R A, Webber J S, Hunt J C, Hojvat S A, Senn D, Devare S G, Decker R H
Hepatitis/AIDS Research Department, Abbott Laboratories, North Chicago, Illinois 60064.
J Infect Dis. 1988 Jan;157(1):149-55. doi: 10.1093/infdis/157.1.149.
We molecularly cloned the gag and env genes of the human immunodeficiency virus (HIV) and expressed fragments of these genes in Escherichia coli. Using the recombinant core and envelope proteins, we developed two competitive immunoassays (CIAs). Samples that recognized either the envelope or core proteins were considered positive for antibodies to HIV. This test system was comparable with western blot in detecting antibodies in patients with AIDS or AIDS-related complex that were repeatably reactive in the HIV screening test. All 360 individuals who were positive by western blot were positive by the CIA. A total of 844 samples repeatably reactive by an ELISA screening test were negative both by western blot and by the CIA; 48 samples positive by ELISA, but negative or indeterminate by western blot, were positive by the CIA. Alternate research procedures verified the positivity of these individuals. These data indicate that the CIA described here may be useful as an adjunct or alternative to the western blot.
我们对人类免疫缺陷病毒(HIV)的gag和env基因进行了分子克隆,并在大肠杆菌中表达了这些基因的片段。利用重组核心蛋白和包膜蛋白,我们开发了两种竞争性免疫测定法(CIA)。识别包膜蛋白或核心蛋白的样本被视为HIV抗体阳性。该检测系统在检测艾滋病或艾滋病相关综合征患者的抗体方面与蛋白质印迹法相当,这些抗体在HIV筛查试验中具有重复性反应性。所有经蛋白质印迹法检测呈阳性的360名个体经CIA检测也呈阳性。共有844份经ELISA筛查试验具有重复性反应性的样本经蛋白质印迹法和CIA检测均为阴性;48份经ELISA检测呈阳性但经蛋白质印迹法检测为阴性或不确定的样本经CIA检测呈阳性。其他研究程序证实了这些个体的阳性结果。这些数据表明,这里描述的CIA可用作蛋白质印迹法的辅助方法或替代方法。