Wu Mingkun, Liu Jiangfeng, Wang Xinming, Zhang Xiaomei, Liang Te, Chen Lan, Huang Tingxuan, Li Yanan, Zheng Chang, Yang Yehong, Wang Jianwei, Yu Xiaobo, Guo Li, Yang Juntao, Ren Lili
National Health Commission Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory Institute of Pathogen Biology Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China.
State Key Laboratory of Medical Molecular Biology Institute of Basic Medical Sciences Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China.
MedComm (2020). 2023 Sep 3;4(5):e361. doi: 10.1002/mco2.361. eCollection 2023 Oct.
The profile of antibodies against antigenic epitopes of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during neutralizing antibody (NAb) decay has not been clarified. Using a SARS-CoV-2 proteome microarray that contained viral antigenic peptides, we analyzed the characteristics of the humoral response in patients with coronavirus disease 19 (COVID-19) in a longitudinal study. A total of 89 patients were recruited, and 226 plasma samples were serially collected in 2020. In the antigenic peptide microarray, the level of immunoglobulin G (IgG) antibodies against peptides within the S2 subunit (S-82) and a conserved gene region in variants of interest, open reading frame protein 10 (ORF10-3), were closely associated with the presence of SARS-CoV-2 NAbs. In an independent evaluation cohort of 232 plasma samples collected from 116 COVID-19 cases in 2020, S82-IgG titers were higher in NAbs-positive samples ( = 0.002) than in NAbs-negative samples using enzyme-linked immunosorbent assay. We further collected 66 plasma samples from another cohort infected by Omicron BA.1 virus in 2022. Compared with the samples with lower S82-IgG titers, NAb titers were significantly higher in the samples with higher S82-IgG titers ( = 0.04). Our findings provide insights into the understanding of the decay-associated signatures of SARS-CoV-2 NAbs.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)中和抗体(NAb)衰减过程中针对其抗原表位的抗体谱尚未明确。在一项纵向研究中,我们使用包含病毒抗原肽的SARS-CoV-2蛋白质组微阵列,分析了19冠状病毒病(COVID-19)患者的体液免疫反应特征。共招募了89名患者,并于2020年连续采集了226份血浆样本。在抗原肽微阵列中,针对S2亚基内肽段(S-82)和关注变异株中一个保守基因区域开放阅读框蛋白10(ORF10-3)的免疫球蛋白G(IgG)抗体水平与SARS-CoV-2 NAb的存在密切相关。在2020年从116例COVID-19病例中采集的232份血浆样本的独立评估队列中,使用酶联免疫吸附测定法,NAb阳性样本中的S82-IgG滴度高于NAb阴性样本(P = 0.002)。我们还于2022年从另一组感染奥密克戎BA.1病毒的队列中进一步采集了66份血浆样本。与S82-IgG滴度较低的样本相比,S82-IgG滴度较高的样本中NAb滴度显著更高(P = 0.04)。我们的研究结果为理解SARS-CoV-2 NAb的衰减相关特征提供了见解。