Systemic immune profiling of Omicron-infected subjects inoculated with different doses of inactivated virus vaccine

生物 接种疫苗 助推器(火箭) 免疫系统 病毒学 增强剂量 免疫学 免疫 病毒 爆发 免疫 天文 物理
作者
Shanhe Yu,Yingni Lin,Yong Li,Shijun Chen,Lina Zhou,Hejie Song,Cuiping Yang,Haiqing Zhang,Jianping Zhou,Shun-Chang Sun,Yanan Li,Juan Chen,Ruixue Feng,Q. L. Niu,Yinyin Xie,Ruihong Zhang,Yin Tong,Sai‐Juan Chen,Qing Yun Li,Jiang Zhu
出处
期刊:Cell [Cell Press]
卷期号:186 (21): 4615-4631.e16 被引量:20
标识
DOI:10.1016/j.cell.2023.08.033
摘要

SARS-CoV-2 primary strain-based vaccination exerts a protective effect against Omicron variants-initiated infection, symptom occurrence, and disease severity in a booster-dependent manner. Yet, the underlying mechanisms remain unclear. During the 2022 Omicron outbreak in Shanghai, we enrolled 122 infected adults and 50 uninfected controls who had been unvaccinated or vaccinated with two or three doses of COVID-19 inactive vaccines and performed integrative analysis of 41-plex CyTOF, RNA-seq, and Olink on their peripheral blood samples. The frequencies of HLA-DRhi classical monocytes, non-classical monocytes, and Th1-like Tem tended to increase, whereas the frequency of Treg was reduced by booster vaccine, and they influenced symptom occurrence in a vaccine dose-dependent manner. Intercorrelation and mechanistic analysis suggested that the booster vaccination induced monocytic training, which would prime monocytic activation and maturation rather than differentiating into myeloid-derived suppressive cells upon Omicron infections. Overall, our study provides insights into how booster vaccination elaborates protective immunity across SARS-CoV-2 variants.
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