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Reduced cross-protective potential of Omicron compared to ancestral SARS-CoV-2 spike vaccines against potentially zoonotic coronaviruses.

npj Viruses. 2024-11; 
Tyler M. Renner, Matthew Stuible, Brian Cass, Sylvie Perret, Julie Guimond, Simon Lord-Dufour, Michael J. McCluskie, Yves Durocher & Bassel Akache
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Gene Synthesis HO codon-optimized sequences encoding spike ectodomains of animalorigin sarbecoviruses (with prefusion-stabilizing 2P mutations) fused to human resistin and purification tags (FLAG-dual-Strep-6His or dualStrep-6His) at the C-terminus were synthesized at Genscript and cloned into the pTT241® plasmid50. The plasmid DNA templates used to generate the tested mRNAs were designed based on the publicly available Pfizer-BioNTech mRNA/LNP vaccine sequence24 and synthesized by Genscript (Piscataway, NJ, USA) in a pUC57 backbone. Get A Quote

摘要

The COVID-19 pandemic has emphasised the importance of vaccines and preparedness against viral threats crossing species barriers. In response, a worldwide vaccination campaign targeting SARS-CoV-2 was implemented, which provides some cross-protective immunological memory to other coronavirus species with zoonotic potential. Following a vaccination regimen against SARS-CoV-2 spike in a preclinical mouse model, we were able to demonstrate the induction of neutralizing antibodies towards multiple human ACE2 (hACE2)-binding Sarbecovirus spikes. Importantly, compared to vaccines based on the SARS-CoV-2 Reference strain, vaccines based on Omicron spike sequences induced drastically less broadly cross-protective neutr... More

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