A Spike-Accum bioconjugate protein vaccine confers potent SARS-CoV-2-specific immunity.

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作者:Pierre Bikorimana Jean, Caveney Nathanael A, El-Hachem Nehme, Mandl Gabrielle A, Capobianco John A, Stanga Daniela, Abusarah Jamilah, Hancock Mark A, Farah Roudy, Gonçalves Marina P, Falzarano Darryl, Liao Mingmin, Hamonic Glenn, Liu Qiang, Beaudoin Simon, Talbot Sebastien, Rafei Moutih
Despite the recent control of COVID-19, the devastating effects caused by the 3-year pandemic highlight the importance of developing effective vaccines to rapidly address future outbreaks. The present study describes a novel Spike (Sp) protein-based vaccine formulation using the Accum platform. Although Sp-Accum bioconjugation does not alter the overall protein structure, it triggers a substantial antibody titer: i) exhibiting higher specificity toward the S1 domain of Sp, ii) neutralizing Sp-ACE2 interactions, and iii) cross-reacting with various Sp variants. Besides validating the vaccine immunogenicity in rabbits, its administration in a "gold-standard" SARS-CoV-2 hamster model was shown to be safe while accelerating viral clearance without eliciting signs of pathological inflammation in the lungs of infected animals. Altogether, this proof-of-concept study not only demonstrates once again the versatility of the Accum technology in vaccine engineering, but it provides an enabling technology for the rapid development of value-added, protein-based vaccines for future pandemics.

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