A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
Autor: | Volkmann, Ariane, Koopman, Gerrit, Mooij, Petra, Verschoor, Ernst J., Verstrepen, Babs E., Bogers, Willy M.J.M., Idorn, Manja, Paludan, Søren R., Vang, Søren, Nielsen, Morten A., Sander, Adam F., Schmittwolf, Carolin, Hochrein, Hubertus, Chaplin, Paul |
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Rok vydání: | 2022 |
Předmět: |
Mice
Inbred BALB C COVID-19 Vaccines SARS-CoV-2 COVID-19/prevention & control Immunology COVID-19 Viral Vaccines variants of concern (VOCs) protection Antibodies Viral Antibodies Neutralizing Macaca mulatta Mice Capsid virus-like particles (VLP) Immunology and Allergy Animals Humans non-human primates (NHP) Capsid Proteins corona broad neutralizing antibodies |
Zdroj: | Front. Immunol Volkmann, A, Koopman, G, Mooij, P, Verschoor, E J, Verstrepen, B E, Bogers, W M J M, Idorn, M, Paludan, S R, Vang, S, Nielsen, M A, Sander, A F, Schmittwolf, C, Hochrein, H & Chaplin, P 2022, ' A capsid virus-like particle-based SARS-CoV-2 vaccine induces high levels of antibodies and protects Rhesus macaques ', Frontiers in Immunology, vol. 13, pp. 857440 . https://doi.org/10.3389/fimmu.2022.857440 Volkmann, A, Koopman, G, Mooij, P, Verschoor, E J, Verstrepen, B E, Bogers, W M J M, Idorn, M, Paludan, S R, Vang, S, Nielsen, M A, Sander, A F, Schmittwolf, C, Hochrein, H & Chaplin, P 2022, ' A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques ', Frontiers in Immunology, vol. 13, 857440 . https://doi.org/10.3389/fimmu.2022.857440 |
ISSN: | 1664-3224 |
DOI: | 10.3389/fimmu.2022.857440 |
Popis: | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a worldwide pandemic. Here, we present non-human primate immunogenicity and protective efficacy data generated with the capsid virus-like particle (cVLP)-based vaccine ABNCoV2 that has previously demonstrated immunogenicity in mice. In rhesus macaques, a single vaccination with either 15 or 100 μg ABNCoV2 induced binding and neutralizing antibodies in a dose-dependent manner, at levels comparable to those measured in human convalescents. A second vaccine administration led to a >50-fold increase in neutralizing antibodies, with 2-log higher mean levels in the 100-μg ABNCoV2 group compared with convalescent samples. Upon SARS-CoV-2 challenge, a significant reduction in viral load was observed for both vaccine groups relative to the challenge control group, with no evidence of enhanced disease. Remarkably, neutralizing antibody titers against an original SARS-CoV-2 isolate and against variants of concern were comparable, indicating a potential for broad protection afforded by ABNCoV2, which is currently in clinical testing. |
Databáze: | OpenAIRE |
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