免疫原性
佐剂
生物
明矾
病毒学
免疫
CpG站点
免疫学
抗体
减毒疫苗
接种疫苗
免疫系统
微生物学
遗传学
毒力
化学
基因
基因表达
有机化学
DNA甲基化
作者
Xiaotong Zheng,Rong Yang,Yuxiu Zhao,Yadan Zhang,Guangying Yuan,Weidong Li,Zhuangzhuang Xiao,Xiaofei Dong,Meng Ma,Yancen Guo,Wei Wang,Xue Zhao,Hongqiang Yang,Shaoting Qiu,Peng Zheng,Ankang Liu,Shouzhi Yu,Yuntao Zhang
出处
期刊:Virology
[Elsevier BV]
日期:2024-03-07
卷期号:594: 110050-110050
标识
DOI:10.1016/j.virol.2024.110050
摘要
The SARS-CoV-2 Omicron variant, which was classified as a variant of concern (VOC) by the World Health Organization on 26 November 2021, has attracted worldwide attention for its high transmissibility and immune evasion ability. The existing COVID-19 vaccine has been shown to be less effective in preventing Omicron variant infection and symptomatic infection, which brings new challenges to vaccine development and application. Here, we evaluated the immunogenicity and safety of an Omicron variant COVID-19 inactivated vaccine containing aluminum and CpG adjuvants in a variety of animal models. The results showed that the vaccine candidate could induce high levels of neutralizing antibodies against the Omicron variant virus and binding antibodies, and significantly promoted cellular immune response. Meanwhile, the vaccine candidate was safe. Therefore, it provided more foundation for the development of aluminum and CpG as a combination adjuvant in human vaccines.
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