| Literature DB >> 35723969 |
Farshad Guirakhoo1, Shixia Wang1, Chang Yi Wang2, Hui Kai Kuo2, Wen Jiun Peng2, Hope Liu2, Lixia Wang1, Marina Johnson3, Adam Hunt3, Mei Mei Hu1, Thomas P Monath1, Alexander Rumyantsev1, David Goldblatt3.
Abstract
The highly transmissible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has caused high rates of breakthrough infections in those previously vaccinated with ancestral strain coronavirus disease 2019 (COVID-19) vaccines. Here, we demonstrate that a booster dose of UB-612 vaccine candidate delivered 7-9 months after primary vaccination increased neutralizing antibody levels by 131-, 61-, and 49-fold against ancestral SARS-CoV-2 and the Omicron BA.1 and BA.2 variants, respectively. Based on the receptor-binding domain protein binding antibody responses, the UB-612 third-dose booster may lead to an estimated approximately 95% efficacy against symptomatic COVID-19 caused by the ancestral strain. Our results support UB-612 as a potential potent booster against current and emerging SARS-CoV-2 variants.Entities:
Keywords: COVID-19; Omicron; SARS-CoV-2; booster; clinical trial; neutralizing antibody; receptor-binding domain; subunit; vaccine; variant
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Year: 2022 PMID: 35723969 PMCID: PMC9278180 DOI: 10.1093/infdis/jiac241
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 7.759