佐剂
明矾
免疫原性
免疫系统
免疫学
CpG寡核苷酸
医学
病毒学
生物
化学
生物化学
基因表达
DNA甲基化
有机化学
基因
作者
Jie Yang,Boran Li,Dongsheng Yang,Jie Wu,Anna Yang,Wenhui Wang,Fengjie Lin,Xin Wan,Yuwei Li,Zhuo Chen,Shiyun Lv,Deqin Pang,Wenbo Liao,Shengli Meng,Jia Lu,Jing Guo,Zejun Wang,Shuo Shen
出处
期刊:Vaccine
[Elsevier BV]
日期:2023-08-26
卷期号:41 (41): 6064-6071
被引量:8
标识
DOI:10.1016/j.vaccine.2023.08.061
摘要
The ongoing evolution and emergence of SARS-CoV-2 variants have raised concerns regarding the efficacy of existing vaccines and therapeutic agents. This study aimed to investigate the immunogenicity of an aluminum hydroxide (Alum) and CpG adjuvanted inactivated vaccine (IAV) candidate against SARS-CoV-2 in mice. A comparison was made between the immune response of mice vaccinated with the Alum+CpG adjuvant IAV and those vaccinated with the Alum adjuvant IAV. Mice immunized with Alum+CpG adjuvant IAV demonstrated high antibody titers and a durable humoral immune response, as well as a Th1-type cellular immune response. Notably, compared to Alum alone vaccine, the Alum+CpG adjuvant IAV induced significantly higher proportions of GC B cells in the splenocytes of immunized mice. Importantly, the changes in inflammatory cytokine levels in the sera of mice vaccinated with the Alum+CpG adjuvant IAV followed a similar trend to that of the Alum adjuvant IAV, which had been proven safe in clinical trials. Overall, our results demonstrate that Alum+CpG adjuvant has the potential to serve as a novel adjuvant, thereby providing valuable insights into the development of vaccine formulations.
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