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Preparation and identification of anti-rabies virus monoclonal antibodies

机译:抗狂犬病病毒单克隆抗体的制备与鉴定

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摘要

To provide a foundation for the development of rapid and specific methods for the diagnosis of rabies virus infection, anti-rabies virus monoclonal antibodies were prepared and rabies virus nucleoprotein and human rabies virus vaccine strain (PV strain) were used as immunogens to immunize 6–8 week old female BALB/c mice. Spleen cells and SP2/0 myeloma cells were fused according to conventional methods: the monoclonal cell strains obtained were selected using the indirect immunofluorescence test; this was followed by preparation of monoclonal antibody ascitic fluid; and finally, systematic identification of subclass, specificity and sensitivity was carried out. Two high potency and specific monoclonal antibodies against rabies virus were obtained and named 3B12 and 4A12, with ascitic fluid titers of 1:8000 and 1:10000, respectively. Both belonged to the IgG2a subclass. These strains secrete potent, stable and specific anti-rabies virus monoclonal antibodies, which makes them well suited for the development of rabies diagnosis reagents.
机译:为开发快速,特异性的狂犬病毒感染诊断方法奠定基础,制备了抗狂犬病毒单克隆抗体,并将狂犬病毒核蛋白和人类狂犬病毒疫苗株(PV株)用作免疫原,对6- 8周大的雌性BALB / c小鼠。按照常规方法融合脾细胞和SP2 / 0骨髓瘤细胞:使用间接免疫荧光试验选择获得的单克隆细胞株;用间接免疫荧光试验选择获得的单克隆细胞株。然后制备单克隆抗体腹水。最后,对亚类,特异性和敏感性进行了系统的鉴定。获得了两种针对狂犬病毒的高效单克隆抗体,分别命名为3B12和4A12,腹水滴度分别为1:8000和1:10000。两者都属于IgG2a亚类。这些菌株分泌有效,稳定和特异性的抗狂犬病病毒单克隆抗体,使其非常适合开发狂犬病诊断试剂。

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