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A self-assembled trimeric protein vaccine induces protective immunity against Omicron variant

Authors :
Cai He
Jingyun Yang
Weiqi Hong
Zimin Chen
Dandan Peng
Hong Lei
Aqu Alu
Xuemei He
Zhenfei Bi
Xiaohua Jiang
Guowen Jia
Yun Yang
Yanan Zhou
Wenhai Yu
Cong Tang
Qing Huang
Mengli Yang
Bai Li
Jingmei Li
Junbin Wang
Haiying Que
Li Chen
Wenyan Ren
Dandan Wan
Jiong Li
Wei Wang
Guobo Shen
Zhiwei Zhao
Li Yang
Jinliang Yang
Zhenling Wang
Zhaoming Su
Yuquan Wei
Xiaobo Cen
Yoshimasa Tanaka
Xiangrong Song
Shuaiyao Lu
Xiaozhong Peng
Guangwen Lu
Xiawei Wei
Source :
Nature Communications. 13
Publication Year :
2022
Publisher :
Springer Science and Business Media LLC, 2022.

Abstract

The recently emerged Omicron (B.1.1.529) variant has rapidly surpassed Delta to become the predominant circulating SARS-CoV-2 variant, given the higher transmissibility rate and immune escape ability, resulting in breakthrough infections in vaccinated individuals. A new generation of SARS-CoV-2 vaccines targeting the Omicron variant are urgently needed. Here, we developed a subunit vaccine named RBD-HR/trimer by directly linking the sequence of RBD derived from the Delta variant (containing L452R and T478K) and HR1 and HR2 in SARS-CoV-2 S2 subunit in a tandem manner, which can self-assemble into a trimer. In multiple animal models, vaccination of RBD-HR/trimer formulated with MF59-like oil-in-water adjuvant elicited sustained humoral immune response with high levels of broad-spectrum neutralizing antibodies against Omicron variants, also inducing a strong T cell immune response in vivo. In addition, our RBD-HR/trimer vaccine showed a strong boosting effect against Omicron variants after two doses of mRNA vaccines, featuring its capacity to be used in a prime-boost regimen. In mice and non-human primates, RBD-HR/trimer vaccination could confer a complete protection against live virus challenge of Omicron and Delta variants. The results qualified RBD-HR/trimer vaccine as a promising next-generation vaccine candidate for prevention of SARS-CoV-2, which deserved further evaluation in clinical trials.

Details

ISSN :
20411723
Volume :
13
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....17ac7a6da3822ba8a9908ced47303a56