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An mRNA vaccine candidate for the SARS-CoV-2 Omicron variant
Jinkai Zang; Chao Zhang; Yannan Yin; Shiqi Xu; Weihua Qiao; Dimitri LAVILLETTE; HaiKun Wang; Zhong Huang.
Afiliação
  • Jinkai Zang; Institut Pasteur of Shanghai Chinese Academy of Sciences
  • Chao Zhang; Institut Pasteur of Shanghai, Chinese Academy of Sciences
  • Yannan Yin; Institut Pasteur of Shanghai, Chinese Academy of Sciences
  • Shiqi Xu; Institut Pasteur of Shanghai, Chinese Academy of Sciences
  • Weihua Qiao; Institut Pasteur of Shanghai, Chinese Academy of Sciences
  • Dimitri LAVILLETTE; Institut Pasteur Shanghai Chine Academy of Sciences
  • HaiKun Wang; Institut Pasteur of Shanghai Chinese Academy of Sciences
  • Zhong Huang; Institut Pasteur of Shanghai
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-479348
ABSTRACT
The newly emerged Omicron variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) contains more than 30 mutations on the spike protein, 15 of which are located within the receptor binding domain (RBD). Consequently, Omicron is able to extensively escape existing neutralizing antibodies and may therefore compromise the efficacy of current vaccines based on the original strain, highlighting the importance and urgency of developing effective vaccines against Omicron. Here we report the rapid generation and evaluation of an mRNA vaccine candidate specific to Omicron. This mRNA vaccine encodes the RBD of Omicron (designated RBD-O) and is formulated with lipid nanoparticle. Two doses of the RBD-O mRNA vaccine efficiently induce neutralizing antibodies in mice; however, the antisera are effective only on the Omicron variant but not on the wildtype and Delta strains, indicating a narrow neutralization spectrum. It is noted that the neutralization profile of the RBD-O mRNA vaccine is opposite to that observed for the mRNA vaccine expressing the wildtype RBD (RBD-WT). Our work demonstrates the feasibility and potency of an RBD-based mRNA vaccine specific to Omicron, providing important information for further development of bivalent or multivalent SARS-CoV-2 vaccines with broad-spectrum efficacy.
Licença
cc_no
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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