Suntronwong Nungruthai, Assawakosri Suvichada, Kanokudom Sitthichai, Yorsaeng Ritthideach, Auphimai Chompoonut, Thongmee Thanunrat, Vichaiwattana Preeyaporn, Duangchinda Thaneeya, Chantima Warangkana, Pakchotanon Pattarakul, Chansaenroj Jira, Nilyanimit Pornjarim, Srimuan Donchida, Thatsanatorn Thaksaporn, Sudhinaraset Natthinee, Wanlapakorn Nasamon, Mongkolsapaya Juthathip, Poovorawan Yong
Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Molecular Biology of Dengue and Flaviviruses Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Development Agency, NSTDA, Pathum Thani 12120, Thailand.
Diagnostics (Basel). 2022 Jul 22;12(8):1781. doi: 10.3390/diagnostics12081781.
This study examined the neutralizing activity and receptor-binding domain (RBD) antibody levels against wild-type and omicron BA.1 and BA.2 variants in individuals who received three doses of COVID-19 vaccination. The relationship between the anti-RBD IgG against wild-type and live virus neutralizing antibody titers against omicron BA.1 and BA.2 variants was examined. In total, 310 sera samples from individuals after booster vaccination (third-dose) were tested for specific IgG wild-type SARS-CoV-2 RBD and the omicron BA.1 surrogate virus neutralization test (sVNT). The live virus neutralization assay against omicron BA.1 and BA.2 was performed using the foci-reduction neutralization test (FRNT50). The anti-RBD IgG strongly correlated with FRNT50 titers against BA.1 and BA.2. Non-linear regression showed that anti-RBD IgG at the cut-off value ≥148 BAU/mL and ≥138 BAU/mL were related to the threshold for FRNT50 titers ≥20 against BA.1 and BA.2, respectively. A moderate correlation was observed between the sVNT and FRNT50 titers. At FRNT50 titers ≥20, the predicted sVNT for BA.1 and BA.2 was ≥10.57% and ≥11.52%, respectively. The study identified anti-RBD IgG and sVNT levels that predict detectable neutralizing antibodies against omicron variants. Assessment and monitoring of protective immunity support vaccine policies and will help identify optimal timing for booster vaccination.
本研究检测了接种三剂新冠疫苗的个体针对野生型、奥密克戎BA.1和BA.2变体的中和活性及受体结合域(RBD)抗体水平。研究了针对野生型的抗RBD IgG与针对奥密克戎BA.1和BA.2变体的活病毒中和抗体滴度之间的关系。总共对310份加强接种(第三剂)个体的血清样本进行了检测,以检测特异性IgG野生型SARS-CoV-2 RBD和奥密克戎BA.1替代病毒中和试验(sVNT)。使用蚀斑减少中和试验(FRNT50)对奥密克戎BA.1和BA.2进行活病毒中和测定。抗RBD IgG与针对BA.1和BA.2的FRNT50滴度密切相关。非线性回归显示,临界值≥148 BAU/mL和≥138 BAU/mL的抗RBD IgG分别与针对BA.1和BA.2的FRNT50滴度≥20的阈值相关。观察到sVNT和FRNT50滴度之间存在中度相关性。在FRNT50滴度≥20时,针对BA.1和BA.2预测的sVNT分别≥10.57%和≥11.52%。该研究确定了可预测针对奥密克戎变体的可检测中和抗体的抗RBD IgG和sVNT水平。对保护性免疫的评估和监测有助于支持疫苗政策,并将有助于确定加强接种的最佳时机。