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- W3201612838 abstract "Abstract Second-generation COVID-19 vaccines could contribute to establish protective immunity against SARS-CoV-2 and its emerging variants. We developed COH04S1, a synthetic multiantigen Modified Vaccinia Ankara-based SARS-CoV-2 vaccine that co-expresses spike and nucleocapsid antigens. Here, we report COH04S1 vaccine efficacy in animal models. We demonstrate that intramuscular or intranasal vaccination of Syrian hamsters with COH04S1 induces robust Th1-biased antigen-specific humoral immunity and cross-neutralizing antibodies (NAb) and protects against weight loss, lower respiratory tract infection, and lung injury following intranasal SARS-CoV-2 challenge. Moreover, we demonstrate that single-dose or two-dose vaccination of non-human primates with COH04S1 induces robust antigen-specific binding antibodies, NAb, and Th1-biased T cells, protects against both upper and lower respiratory tract infection following intranasal/intratracheal SARS-CoV-2 challenge, and triggers potent post-challenge anamnestic antiviral responses. These results demonstrate COH04S1-mediated vaccine protection in animal models through different vaccination routes and dose regimens, complementing ongoing investigation of this multiantigen SARS-CoV-2 vaccine in clinical trials." @default.
- W3201612838 created "2021-09-27" @default.
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- W3201612838 date "2021-09-15" @default.
- W3201612838 modified "2023-10-07" @default.
- W3201612838 title "Synthetic Multiantigen MVA Vaccine COH04S1 Protects Against SARS-CoV-2 in Syrian Hamsters and Non-Human Primates" @default.
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- W3201612838 doi "https://doi.org/10.1101/2021.09.15.460487" @default.
- W3201612838 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8452095" @default.
- W3201612838 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34545366" @default.
- W3201612838 hasPublicationYear "2021" @default.
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