Yu Pengcheng, Tao Xiaoyan, Wang Lihua, Tang Qing, Liu Shuqing, Zhu Wuyang
Bing Du Xue Bao. 2016 Nov;32(6):790-5.
To establish a method for measurement of the neutralizing activity of a monoclonal antibody against the rabies virus. Twenty-four rabies street virus-positive samples were isolated by the mouse inoculation test. Isolated rabies street viruses were cultured and the virus titer tested in N2A cells. We established a rabies street virus bank with viruses that could adapt to the growth of N2A cells with a high titer. Then repeatability was evaluated after three detections of the TRN006 monoclonal antibody. Of the 24 positive samples,15 strains of the virus could adapt to N2A cells and form fluorescent foci in cells.Finally,10 strains with a high titer were selected for the rabies street virus bank, which covered nine Provinces of China and four Chinese lineages. Three lineages were used for the neutralization test for the monoclonal antibody, and the Student’s t-test showed that it had good repeatability.
建立一种检测单克隆抗体对狂犬病病毒中和活性的方法。通过小鼠接种试验分离出24份狂犬病街毒株阳性样本。对分离出的狂犬病街毒株进行培养,并在N2A细胞中检测病毒滴度。我们用能够适应在N2A细胞中高滴度生长的病毒建立了一个狂犬病街毒株库。然后对TRN006单克隆抗体进行三次检测后评估其重复性。在24份阳性样本中,有15株病毒能够适应N2A细胞并在细胞中形成荧光灶。最后,从覆盖中国九个省份和四个中国谱系的毒株中选择10株高滴度毒株用于狂犬病街毒株库。使用三个谱系对该单克隆抗体进行中和试验,学生t检验表明其具有良好的重复性。