Frontiers in Immunology (May 2023)

SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern

  • Qinhai Ma,
  • Man Li,
  • Lin Ma,
  • Caroline Zhang,
  • Hong Zhang,
  • Huiling Zhong,
  • Jian Wen,
  • Yongsheng Wang,
  • Zewei Yan,
  • Wei Xiong,
  • Linping Wu,
  • Jianmin Guo,
  • Wei Yang,
  • Zifeng Yang,
  • Zifeng Yang,
  • Biliang Zhang,
  • Biliang Zhang,
  • Biliang Zhang

DOI
https://doi.org/10.3389/fimmu.2023.1195299
Journal volume & issue
Vol. 14

Abstract

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IntroductionThe severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has rapidly spread around the globe. With a substantial number of mutations in its Spike protein, the SARS-CoV-2 Omicron variant is prone to immune evasion and led to the reduced efficacy of approved vaccines. Thus, emerging variants have brought new challenges to the prevention of COVID-19 and updated vaccines are urgently needed to provide better protection against the Omicron variant or other highly mutated variants.Materials and methodsHere, we developed a novel bivalent mRNA vaccine, RBMRNA-405, comprising a 1:1 mix of mRNAs encoding both Delta-derived and Omicron-derived Spike proteins. We evaluated the immunogenicity of RBMRNA-405 in BALB/c mice and compared the antibody response and prophylactic efficacy induced by monovalent Delta or Omicron-specific vaccine with the bivalent RBMRNA-405 vaccine in the SARSCoV-2 variant challenge.ResultsResults showed that the RBMRNA-405 vaccine could generate broader neutralizing antibody responses against both Wuhan-Hu-1 and other SARS-CoV-2 variants, including Delta, Omicron, Alpha, Beta, and Gamma. RBMRNA-405 efficiently blocked infectious viral replication and lung injury in both Omicron- and Delta-challenged K18-ACE2 mice.ConclusionOur data suggest that RBMRNA-405 is a promising bivalent SARS-CoV-2 vaccine with broad-spectrum efficacy for further clinical development.

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