Shanghai Institute of Hematology, National Research Center for Translational Medicine, State Key Laboratory of Medical Genomics, Ruijin Hospital Affiliated to Shanghai Jiao Tong University (SJTU) School of Medicine, Shanghai, 200025, China.
National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, China.
Front Med. 2023 Jun;17(3):562-575. doi: 10.1007/s11684-022-0977-3. Epub 2023 Mar 23.
The Omicron family of SARS-CoV-2 variants are currently driving the COVID-19 pandemic. Here we analyzed the clinical laboratory test results of 9911 Omicron BA.2.2 sublineages-infected symptomatic patients without earlier infection histories during a SARS-CoV-2 outbreak in Shanghai in spring 2022. Compared to an earlier patient cohort infected by SARS-CoV-2 prototype strains in 2020, BA.2.2 infection led to distinct fluctuations of pathophysiological markers in the peripheral blood. In particular, severe/critical cases of COVID-19 post BA.2.2 infection were associated with less pro-inflammatory macrophage activation and stronger interferon alpha response in the bronchoalveolar microenvironment. Importantly, the abnormal biomarkers were significantly subdued in individuals who had been immunized by 2 or 3 doses of SARS-CoV-2 prototype-inactivated vaccines, supporting the estimation of an overall 96.02% of protection rate against severe/critical disease in the 4854 cases in our BA.2.2 patient cohort with traceable vaccination records. Furthermore, even though age was a critical risk factor of the severity of COVID-19 post BA.2.2 infection, vaccination-elicited protection against severe/critical COVID-19 reached 90.15% in patients aged ≽ 60 years old. Together, our study delineates the pathophysiological features of Omicron BA.2.2 sublineages and demonstrates significant protection conferred by prior prototype-based inactivated vaccines.
奥密克戎家族的 SARS-CoV-2 变体目前正在推动 COVID-19 大流行。在这里,我们分析了 2022 年春季上海 SARS-CoV-2 爆发期间 9911 名无既往感染史的感染奥密克戎 BA.2.2 亚谱系的有症状患者的临床实验室检测结果。与 2020 年感染 SARS-CoV-2 原型株的早期患者队列相比,BA.2.2 感染导致外周血中病理生理标志物的明显波动。特别是,COVID-19 后 BA.2.2 感染的重症/危重症病例与支气管肺泡微环境中促炎巨噬细胞激活减少和干扰素α反应增强有关。重要的是,在接受 2 或 3 剂 SARS-CoV-2 原型灭活疫苗免疫的个体中,异常生物标志物明显减弱,支持对我们 BA.2.2 患者队列中 4854 例有可追溯疫苗接种记录的个体的严重/危重症疾病的总体 96.02%的保护率估计。此外,尽管年龄是 COVID-19 后 BA.2.2 感染严重程度的关键危险因素,但疫苗接种对 COVID-19 重症/危重症的保护作用在年龄≧60 岁的患者中达到 90.15%。总之,我们的研究描绘了奥密克戎 BA.2.2 亚谱系的病理生理特征,并证明了先前基于原型的灭活疫苗提供的显著保护作用。