| Literature DB >> 32511417 |
Jesse H Erasmus1,2, Amit P Khandhar2,3, Alexandra C Walls4, Emily A Hemann5,6, Megan A O'Connor1,7, Patience Murapa1, Jacob Archer1,3, Shanna Leventhal8, Jim Fuller1, Thomas Lewis1,7, Kevin E Draves1, Samantha Randall3, Kathryn A Guerriero7, Malcolm S Duthie2, Darrick Carter2,3,5, Steven G Reed3,5, David W Hawman8, Heinz Feldmann8, Michael Gale5,7,6, David Veesler4, Peter Berglund2, Deborah Heydenburg Fuller1,5,7.
Abstract
The ongoing COVID-19 pandemic, caused by infection with SARS-CoV-2, is having a dramatic and deleterious impact on health services and the global economy. Grim public health statistics highlight the need for vaccines that can rapidly confer protection after a single dose and be manufactured using components suitable for scale-up and efficient distribution. In response, we have rapidly developed repRNA-CoV2S, a stable and highly immunogenic vaccine candidate comprised of an RNA replicon formulated with a novel Lipid InOrganic Nanoparticle (LION) designed to enhance vaccine stability, delivery and immunogenicity. We show that intramuscular injection of LION/repRNA-CoV2S elicits robust anti-SARS-CoV-2 spike protein IgG antibody isotypes indicative of a Type 1 T helper response as well as potent T cell responses in mice. Importantly, a single-dose administration in nonhuman primates elicited antibody responses that potently neutralized SARS-CoV-2. These data support further development of LION/repRNA-CoV2S as a vaccine candidate for prophylactic protection from SARS-CoV-2 infection.Entities:
Keywords: RNA; SARS-CoV-2; coronavirus; nanoparticle; nonhuman primates; replicon; vaccine
Year: 2020 PMID: 32511417 PMCID: PMC7265689 DOI: 10.1101/2020.05.28.121640
Source DB: PubMed Journal: bioRxiv