Goodger B V, Waltisbuhl D J, Wright I G, White M
CSIRO Division of Tropical Animal Production, Long Pocket Laboratories, Indooroopilly, Queensland, Australia.
Int J Parasitol. 1992 Jul;22(4):533-5. doi: 10.1016/0020-7519(92)90156-f.
Murine monoclonal antibodies (MAB) were produced against the 'beta' fraction of Babesia bovis. A MAB, W11C5, selected on the criterion of its staining of erythrocytes infected with B. bovis, was purified. The antigen identified by MAB W11C5 was extracted from B. bovis infected erythrocytes by affinity chromatography and used in a vaccination trial to test its vaccine efficacy against homologous B. bovis infection in splenectomized calves. The vaccinated group showed significantly different parasitaemias from the control group and it was concluded that the B. bovis antigen 11C5 induced a protective immune response when used as a vaccine. This antigen should be synthesized using recombinant DNA techniques to determine its efficacy and suitability as a commercial vaccine against B. bovis infection.
制备了针对牛巴贝斯虫“β”组分的鼠单克隆抗体(MAB)。选择了一株基于其对感染牛巴贝斯虫的红细胞染色标准筛选出的单克隆抗体W11C5并进行了纯化。通过亲和层析从感染牛巴贝斯虫的红细胞中提取出由单克隆抗体W11C5识别的抗原,并将其用于疫苗试验,以测试其对脾切除小牛同源牛巴贝斯虫感染的疫苗效力。接种疫苗组的虫血症与对照组有显著差异,得出结论:牛巴贝斯虫抗原11C5用作疫苗时可诱导保护性免疫反应。应使用重组DNA技术合成该抗原,以确定其作为抗牛巴贝斯虫感染商业疫苗的效力和适用性。