生物结合
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
穗蛋白
2019年冠状病毒病(COVID-19)
免疫
2019-20冠状病毒爆发
Spike(软件开发)
病毒学
冠状病毒
计算生物学
生物
化学
免疫系统
免疫学
医学
计算机科学
传染病(医学专业)
生物化学
疾病
软件工程
病理
爆发
作者
Jean Pierre Bikorimana,Nathanael A. Caveney,Nehme El‐Hachem,Gabrielle A. Mandl,John A. Capobianco,Daniela Stanga,Jamilah Abusarah,Mark A. Hancock,Roudy Farah,Marina P. Gonçalves,Darryl Falzarano,Mingmin Liao,Glenn Hamonic,Qiang Liu,Simon Beaudoin,Sébastien Talbot,Moutih Rafei
出处
期刊:iScience
[Elsevier]
日期:2025-08-07
卷期号:28 (9): 113314-113314
标识
DOI:10.1016/j.isci.2025.113314
摘要
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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