He Yongquan, Yin Yi, Zhang Yi, Yang Huiping, Jiang Zhiling, Hao Fang, Zhao Taiqiang, Liu Xiaobin, Liu Yusong, Zeng Yong, Li Xi, Chen Xuemei, Xu Kaiju, Tan Chang, Yang Jie, Jiang Li, Gong Bo, Yang Zhenglin
Sichuan Provincial Key Laboratory for Human Disease Gene Study, Center for Medical Genetics, Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Research Unit for Blindness Prevention of Chinese Academy of Medical Sciences (2019RU026), Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Signal Transduct Target Ther. 2025 Jul 30;10(1):242. doi: 10.1038/s41392-025-02319-3.
From December 2022 to January 2023, the SARS-CoV-2 Omicron BA.5/BF.7 variant significantly impacted mainland China. While most COVID-19 patients experienced mild symptoms and were treated as outpatients or at home, some cases progressed to severe illness, necessitating hospitalization or even resulting in death. To better understand this outbreak and forecast future waves as SARS-CoV-2 continues to evolve, it is crucial to assess the titer of neutralizing antibodies (Nab) for evaluating the establishment of an immune barrier. In this study, we investigated the dynamic evolution of humoral immunity following the breakthrough infection wave driven by the SARS-CoV-2 Omicron BA.5/BF.7 variant in southwest China. Over a period of more than one year, we analyzed 3128 serum samples collected monthly to delineate the kinetics of Nab responses in a large cohort. Our data revealed a pronounced surge in Nab titers immediately after the December 2022-January 2023 outbreak, particularly among individuals primed with two or three doses of vaccine. As the epidemic progressed, emerging variants such as XBB.1.5, EG.5, and JN.1 elicited distinct immunological responses and demonstrated varying capacities for immune escape. Our findings underscore the rapid antigenic evolution of SARS-CoV-2 and the consequent challenges in sustaining effective population-level immunity, thereby advocating for continual surveillance and adaptive vaccine immunogen updates.
2022年12月至2023年1月,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎BA.5/BF.7变异株对中国大陆产生了重大影响。虽然大多数冠状病毒病患者症状较轻,作为门诊患者接受治疗或居家治疗,但一些病例进展为重症,需要住院治疗甚至导致死亡。为了更好地了解此次疫情,并在SARS-CoV-2持续进化的情况下预测未来疫情浪潮,评估中和抗体(Nab)滴度对于评估免疫屏障的建立至关重要。在本研究中,我们调查了中国西南部由SARS-CoV-2奥密克戎BA.5/BF.7变异株引发的突破性感染浪潮后体液免疫的动态演变。在一年多的时间里,我们分析了每月收集的3128份血清样本,以描绘一大群人中Nab反应的动力学。我们的数据显示,在2022年12月至2023年1月疫情爆发后,Nab滴度立即显著上升,尤其是在接种了两剂或三剂疫苗的个体中。随着疫情的发展,XBB.1.5、EG.5和JN.1等新出现的变异株引发了不同的免疫反应,并表现出不同的免疫逃逸能力。我们的研究结果强调了SARS-CoV-2快速的抗原进化以及在维持有效的群体水平免疫方面随之而来的挑战,从而提倡持续监测和适应性疫苗免疫原更新。