作者
Neil C Dalvie, Sergio A Rodriguez-Aponte, Brittany L Hartwell, Lisa H Tostanoski, Andrew M Biedermann, Laura E Crowell, Kawaljit Kaur, Ozan S Kumru, Lauren Carter, Jingyou Yu, Aiquan Chang, Katherine McMahan, Thomas Courant, Celia Lebas, Ashley A Lemnios, Kristen A Rodrigues, Murillo Silva, Ryan S Johnston, Christopher A Naranjo, Mary Kate Tracey, Joseph R Brady, Charles A Whittaker, Dongsoo Yun, Natalie Brunette, Jing Yang Wang, Carl Walkey, Brooke Fiala, Swagata Kar, Maciel Porto, Megan Lok, Hanne Andersen, Mark G Lewis, Kerry R Love, Danielle L Camp, Judith Maxwell Silverman, Harry Kleanthous, Sangeeta B Joshi, David B Volkin, Patrice M Dubois, Nicolas Collin, Neil P King, Dan H Barouch, Darrell J Irvine, J Christopher Love
发表日期
2021/9/21
期刊
Proceedings of the National Academy of Sciences
卷号
118
期号
38
页码范围
e2106845118
出版商
National Academy of Sciences
简介
Global containment of COVID-19 still requires accessible and affordable vaccines for low- and middle-income countries (LMICs). Recently approved vaccines provide needed interventions, albeit at prices that may limit their global access. Subunit vaccines based on recombinant proteins are suited for large-volume microbial manufacturing to yield billions of doses annually, minimizing their manufacturing cost. These types of vaccines are well-established, proven interventions with multiple safe and efficacious commercial examples. Many vaccine candidates of this type for SARS-CoV-2 rely on sequences containing the receptor-binding domain (RBD), which mediates viral entry to cells via ACE2. Here we report an engineered sequence variant of RBD that exhibits high-yield manufacturability, high-affinity binding to ACE2, and enhanced immunogenicity after a single dose in mice compared to the Wuhan-Hu-1 …
引用总数
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NC Dalvie, SA Rodriguez-Aponte, BL Hartwell… - Proceedings of the National Academy of Sciences, 2021