Chimeric mRNA-based COVID-19 vaccine induces protective immunity against Omicron and Delta variants

Autor: Qidong Hu, Ying Zhao, Namir Shaabani, Xiaoxuan Lyu, Colin Powers, Haotian Sun, Vincent Cruz, Karen Stegman, Jia Xu, Amber Fossier, Yu Huang, Giang Ho, Yi Kao, Zhihao Wang, Zhenping Wang, Yue Hu, Yi Zheng, Lilian Kyaw, Cipriano Zuluaga, Hua Wang, Hong Pei, Robert Allen, Hui Xie, Henry Ji, Runqiang Chen
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Molecular Therapy: Nucleic Acids, Vol 30, Iss , Pp 465-476 (2022)
Druh dokumentu: article
ISSN: 2162-2531
DOI: 10.1016/j.omtn.2022.10.021
Popis: The emerging SARS-CoV-2 variants of concern (VOCs) exhibit enhanced transmission and immune escape, reducing the effectiveness of currently approved mRNA vaccines. To achieve wider coverage of VOCs, we first constructed a cohort of mRNAs harboring a furin cleavage mutation in the spike (S) protein of predominant VOCs, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), and Delta (B.1.617.2). The mutation abolished the cleavage between the S1 and S2 subunits. Systematic evaluation in vaccinated mice discovered that individual VOC mRNAs elicited strong neutralizing activity in a VOC-specific manner. In particular, the neutralizing antibodies (nAb) produced by immunization with Beta-Furin and Washington (WA)-Furin mRNAs showed potent cross-reactivity with other VOCs. However, neither mRNA elicited strong neutralizing activity against the Omicron variant. Hence, we further developed an Omicron-specific mRNA vaccine that restored protection against the original Omicron variant and some sublineages. Finally, to broaden the protection spectrum of the new Omicron mRNA vaccine, we engineered an mRNA-based chimeric immunogen by introducing the receptor-binding domain of Delta variant into the entire S antigen of Omicron. The resultant chimeric mRNA induced potent and broadly nAbs against Omicron and Delta, which paves the way to developing new vaccine candidates to target emerging variants in the future.
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