Siakkou H, Platzer C, Beier D, Olechnowitz A F, Rosenthal S
Zentralinstitut für Molekularbiologie Berlin-Buch, Akademie der Wissenschaften, DDR.
Arch Exp Veterinarmed. 1990;44(2):223-31.
A highly specific monoclonal antibody (mAb) directed against envelope protein gp51 and effectively bonding the antigen (Ag) on account of its high affinity from an unpurified Ag preparation was chosen for use in a double-sandwich enzyme immuno-assay (EIA) for diagnosis of bovine leukaemia virus (BLV). The epitopes recognised in bovine sera by the gp51-specific antibodies were at the same time properly exposed. Some parameters of major importance to testing were optimised (Ab and Ag quantities, dilution of bovine sera for testing). Preliminary testing of the double-sandwich EIA on selected bovine sera and comparison with both the immunodiffusion test and anti-BLV EIA confirmed its good diagnostic specificity and sensitivity. Hence, this double-sandwich EIA, developed by means of an mAB against gp51, on account of the possibility to use as Ag culture supernatant of the FLC cell line, is a sensitive, low-cost alternative to the anti-BLV EIA Dessau MTP which had so far been used. The double-sandwich EIA is recommended for use in final sanitation for its high analytical and diagnostic sensitivity.
一种针对包膜蛋白gp51的高特异性单克隆抗体(mAb),因其对未纯化抗原制剂具有高亲和力而能有效结合抗原(Ag),被选用于双夹心酶免疫分析(EIA)以诊断牛白血病病毒(BLV)。gp51特异性抗体在牛血清中识别的表位同时能适当暴露。对检测至关重要的一些参数进行了优化(抗体和抗原量、用于检测的牛血清稀释度)。在选定的牛血清上对双夹心EIA进行初步检测,并与免疫扩散试验和抗BLV EIA进行比较,证实了其良好的诊断特异性和敏感性。因此,这种借助针对gp51的单克隆抗体开发的双夹心EIA,由于有可能使用FLC细胞系的培养上清液作为抗原,是一种对迄今使用的抗BLV EIA Dessau MTP而言敏感、低成本的替代方法。双夹心EIA因其高分析和诊断敏感性而被推荐用于最终卫生检测。