Dreitz M J, Dow S W, Fiscus S A, Hoover E A
Department of Pathology, Colorado State University, Fort Collins 80523, USA.
Am J Vet Res. 1995 Jun;56(6):764-8.
We generated monoclonal antibodies (MAB) against feline immunodeficiency virus (FIV) and characterized these MAB by single competition enzyme immunoassays (EIA), immunoblot analysis, and radioimmunoprecipitation. Four MAB identified 3 distinct epitopes of the FIV p24/26 gag major core protein. One MAB recognized the p16/17 gag protein; none recognized envelope proteins. We developed an FIV p26 antigen capture EIA that proved more sensitive (0.5 ng of p26/ml), less expensive, and less time-consuming than reverse transcriptase assay. The same MAB were used to develop an antibody EIA specific for FIV p26. The MAB and capture assays reported should prove useful in FIV diagnosis and research.
我们制备了针对猫免疫缺陷病毒(FIV)的单克隆抗体(MAB),并通过单竞争酶免疫测定(EIA)、免疫印迹分析和放射免疫沉淀对这些单克隆抗体进行了表征。四种单克隆抗体鉴定出了FIV p24/26 gag主要核心蛋白的3个不同表位。一种单克隆抗体识别p16/17 gag蛋白;没有一种识别包膜蛋白。我们开发了一种FIV p26抗原捕获EIA,事实证明它比逆转录酶测定更灵敏(0.5 ng p26/ml)、成本更低且耗时更少。相同的单克隆抗体被用于开发针对FIV p26的抗体EIA。所报道的单克隆抗体和捕获测定在FIV诊断和研究中应会很有用。