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A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques

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 m...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037084/
https://www.ncbi.nlm.nih.gov/pubmed/35479095
http://dx.doi.org/10.3389/fimmu.2022.857440
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author 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
author_facet 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
author_sort Volkmann, Ariane
collection PubMed
description 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.
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spelling pubmed-90370842022-04-26 A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques 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 Front Immunol Immunology 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. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9037084/ /pubmed/35479095 http://dx.doi.org/10.3389/fimmu.2022.857440 Text en Copyright © 2022 Volkmann, Koopman, Mooij, Verschoor, Verstrepen, Bogers, Idorn, Paludan, Vang, Nielsen, Sander, Schmittwolf, Hochrein and Chaplin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
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
A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title_full A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title_fullStr A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title_full_unstemmed A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title_short A Capsid Virus-Like Particle-Based SARS-CoV-2 Vaccine Induces High Levels of Antibodies and Protects Rhesus Macaques
title_sort capsid virus-like particle-based sars-cov-2 vaccine induces high levels of antibodies and protects rhesus macaques
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037084/
https://www.ncbi.nlm.nih.gov/pubmed/35479095
http://dx.doi.org/10.3389/fimmu.2022.857440
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