Objective To establish a Plaque-reduction Neutralization Test(PRNT)for the detection of neutralizing antibody titers of Human Respiratory Syncytial Virus(HRSV)and optimize the conditions for preliminary application.Methods The CHO expression system was used to produce palivizumab monoclonal antibody(palivizumab)and the influencing factors such as cell type,cell culture duration,fixation and permeabilization protocols,and blocking agents.The reproducibility of the method was verified and its correlation was verified with conventional PRNT.Finally,the optimized PRNT assay was further used to determine neutralizing antibody titers against HRSV subtypes A and B in BALB/c mouse serum(immunized by intramuscular injection of HRSV fusion proteins).Results Palivizumab was expressed at approximately 50 mg/L.The optimal working conditions for PRNT were as follows:culturing HEp-2 cells for 2 days,fixing with 4％(V/V)paraformaldehyde at room temperature for 15 min followed by 0.2％(V/V)Triton X-100 permeabilization for 15 minutes as the optimal fixation-permeabilization and removing the blocking step.The overall coefficient of variation(CV)for the reproducibility validation of this method was＜15％,showing a good linear relationship with the conventional PRNT.The Spearman correlation coefficient rs was 0.983.This method was used to detect neutralizing antibody titers in mouse sera against HRSV subtype A strain long and subtype B strain 9320,and the fusion proteins combined with AlOH and CpG adjuvant induced the highest neutralizing antibody titers in mice.Conclusion The HRSV neutralizing antibody assay established in this study is rapid,reproducible,high-throughput,and can be used to detect neutralizing antibodies to HRSV subtypes A and B.
关键词
人呼吸道合胞病毒/免疫染色/噬斑减少中和实验/中和抗体
Key words
Human respiratory syncytial virus/Immunostaining/Plaque reduction neutralization test/Neutralizing antibody
维普
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