A trimeric spike-based COVID-19 vaccine candidate induces broad neutralization against SARS-CoV-2 variants

被引:2
|
作者
Gao, Feixia [1 ]
Zheng, Mei [1 ]
Fan, Jiangfeng [1 ]
Ding, Yahong [1 ]
Liu, Xueying [1 ]
Zhang, Min [1 ]
Zhang, Xin [1 ]
Dong, Jinrong [1 ]
Zhou, Xu [1 ]
Luo, Jian [1 ,2 ]
Li, Xiuling [1 ,2 ]
机构
[1] Shanghai Inst Biol Prod, Dept Res & Dev, Shanghai, Peoples R China
[2] Shanghai Inst Biol Prod, Dept Res & Dev, 350 Anshun Rd, Shanghai 200052, Peoples R China
关键词
SARS-CoV-2; vaccine; S-Trimer protein; CpG; aluminum hydroxide adjuvant; cross-neutralization; DOUBLE-BLIND; ADJUVANTS;
D O I
10.1080/21645515.2023.2186110
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
COVID-19 pandemic caused by SARS-CoV-2 infection has an impact on global public health and social economy. The emerging immune escape of SARS-CoV-2 variants pose great challenges to the development of vaccines based on original strains. The development of second-generation COVID-19 vaccines to induce immune responses with broad-spectrum protective effects is a matter of great urgency. Here, a prefusion-stabilized spike (S) trimer protein based on B.1.351 variant was expressed and prepared with CpG7909/aluminum hydroxide dual adjuvant to investigate the immunogenicity in mice. The results showed that the candidate vaccine could induce a significant receptor binding domain-specific antibody response and a substantial interferon-gamma-mediated immune response. Furthermore, the candidate vaccine also elicited robust cross-neutralization against the pseudoviruses of the original strain, Beta variant, Delta variant and Omicron variant. The vaccine strategy of S-trimer protein formulated with CpG7909/aluminum hydroxide dual adjuvant may be considered a means to increase vaccine effectiveness against future variants.
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页数:8
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