{"title":"Development of monoclonal antibodies suitable for rabies virus antibody and antigen detection.","authors":"Vishal Chander, R P Singh, P C Verma","doi":"10.1007/s13337-012-0096-x","DOIUrl":null,"url":null,"abstract":"<p><p>The control of an infectious viral disease as rabies is made easier by rapid and accurate diagnosis. Successful rabies prophylaxis is dependent upon the active immunization with vaccine along with passive administration of rabies virus neutralizing antibodies which together clear the virus before widespread infection of central nervous system occurs. The present study aimed at the development of monoclonal antibodies (MAbs) suitable for rabies virus antibody and antigen detection. For the production of rabies specific MAbs, immunization of Swiss albino mice with a commercially available vaccine was done and Polyethylene glycol mediated fusion of spleenocytes with myeloma cells was performed. The positive clones were selected on the basis of distinct reactivity by cell Enzyme linked immunosorbent assay and fluorescence in Indirect Fluorescent antibody test. The positive clones obtained were subjected to single cell cloning by limiting dilution method. The reactive clones were further titrated and employed for virus titration and virus neutralization. The neutralizing activity was evaluated using Fluorescence Activated Cell Sorter technique. Three MAb clones showed a distinct percent inhibition in the presence of positive serum. One of the MAb clone No. 5C3 was relatively more specific in detecting rabies antibodies and also found suitable for competitive ELISA to assess the antibody level in vaccinated subjects. </p>","PeriodicalId":50370,"journal":{"name":"Indian Journal of Virology","volume":"23 3","pages":"317-25"},"PeriodicalIF":0.0000,"publicationDate":"2012-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3550790/pdf/13337_2012_Article_96.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s13337-012-0096-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/9/26 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The control of an infectious viral disease as rabies is made easier by rapid and accurate diagnosis. Successful rabies prophylaxis is dependent upon the active immunization with vaccine along with passive administration of rabies virus neutralizing antibodies which together clear the virus before widespread infection of central nervous system occurs. The present study aimed at the development of monoclonal antibodies (MAbs) suitable for rabies virus antibody and antigen detection. For the production of rabies specific MAbs, immunization of Swiss albino mice with a commercially available vaccine was done and Polyethylene glycol mediated fusion of spleenocytes with myeloma cells was performed. The positive clones were selected on the basis of distinct reactivity by cell Enzyme linked immunosorbent assay and fluorescence in Indirect Fluorescent antibody test. The positive clones obtained were subjected to single cell cloning by limiting dilution method. The reactive clones were further titrated and employed for virus titration and virus neutralization. The neutralizing activity was evaluated using Fluorescence Activated Cell Sorter technique. Three MAb clones showed a distinct percent inhibition in the presence of positive serum. One of the MAb clone No. 5C3 was relatively more specific in detecting rabies antibodies and also found suitable for competitive ELISA to assess the antibody level in vaccinated subjects.
通过快速准确的诊断,可以更容易地控制狂犬病这种传染性病毒疾病。狂犬病的成功预防有赖于疫苗的主动免疫和狂犬病病毒中和抗体的被动免疫,两者结合才能在中枢神经系统广泛感染之前清除病毒。本研究旨在开发适用于狂犬病病毒抗体和抗原检测的单克隆抗体(MAbs)。为了生产狂犬病特异性 MAbs,用市售疫苗对瑞士白化小鼠进行了免疫接种,并进行了聚乙二醇介导的脾细胞与骨髓瘤细胞的融合。根据细胞酶联免疫吸附试验的明显反应性和间接荧光抗体试验的荧光筛选出阳性克隆。获得的阳性克隆通过极限稀释法进行单细胞克隆。对反应克隆进行进一步滴定,并用于病毒滴定和病毒中和。使用荧光激活细胞分拣技术对中和活性进行了评估。在阳性血清存在的情况下,三个 MAb 克隆显示出明显的抑制百分比。其中 5C3 号 MAb 克隆在检测狂犬病抗体方面具有更高的特异性,也适用于竞争性 ELISA 法评估接种者的抗体水平。