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Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity
The rapid development of a SARS-CoV-2 vaccine is a global priority. Here, we develop two capsid-like particle (CLP)-based vaccines displaying the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein. RBD antigens are displayed on AP205 CLPs through a split-protein Tag/Catcher, ensuring unid...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804149/ https://www.ncbi.nlm.nih.gov/pubmed/33436573 http://dx.doi.org/10.1038/s41467-020-20251-8 |
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author | Fougeroux, Cyrielle Goksøyr, Louise Idorn, Manja Soroka, Vladislav Myeni, Sebenzile K. Dagil, Robert Janitzek, Christoph M. Søgaard, Max Aves, Kara-Lee Horsted, Emma W. Erdoğan, Sayit Mahmut Gustavsson, Tobias Dorosz, Jerzy Clemmensen, Stine Fredsgaard, Laurits Thrane, Susan Vidal-Calvo, Elena E. Khalifé, Paul Hulen, Thomas M. Choudhary, Swati Theisen, Michael Singh, Susheel K. Garcia-Senosiain, Asier Van Oosten, Linda Pijlman, Gorben Hierzberger, Bettina Domeyer, Tanja Nalewajek, Blanka W. Strøbæk, Anette Skrzypczak, Magdalena Andersson, Laura F. Buus, Søren Buus, Anette Stryhn Christensen, Jan Pravsgaard Dalebout, Tim J. Iversen, Kasper Harritshøj, Lene H. Mordmüller, Benjamin Ullum, Henrik Reinert, Line S. de Jongh, Willem Adriaan Kikkert, Marjolein Paludan, Søren R. Theander, Thor G. Nielsen, Morten A. Salanti, Ali Sander, Adam F. |
author_facet | Fougeroux, Cyrielle Goksøyr, Louise Idorn, Manja Soroka, Vladislav Myeni, Sebenzile K. Dagil, Robert Janitzek, Christoph M. Søgaard, Max Aves, Kara-Lee Horsted, Emma W. Erdoğan, Sayit Mahmut Gustavsson, Tobias Dorosz, Jerzy Clemmensen, Stine Fredsgaard, Laurits Thrane, Susan Vidal-Calvo, Elena E. Khalifé, Paul Hulen, Thomas M. Choudhary, Swati Theisen, Michael Singh, Susheel K. Garcia-Senosiain, Asier Van Oosten, Linda Pijlman, Gorben Hierzberger, Bettina Domeyer, Tanja Nalewajek, Blanka W. Strøbæk, Anette Skrzypczak, Magdalena Andersson, Laura F. Buus, Søren Buus, Anette Stryhn Christensen, Jan Pravsgaard Dalebout, Tim J. Iversen, Kasper Harritshøj, Lene H. Mordmüller, Benjamin Ullum, Henrik Reinert, Line S. de Jongh, Willem Adriaan Kikkert, Marjolein Paludan, Søren R. Theander, Thor G. Nielsen, Morten A. Salanti, Ali Sander, Adam F. |
author_sort | Fougeroux, Cyrielle |
collection | PubMed |
description | The rapid development of a SARS-CoV-2 vaccine is a global priority. Here, we develop two capsid-like particle (CLP)-based vaccines displaying the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein. RBD antigens are displayed on AP205 CLPs through a split-protein Tag/Catcher, ensuring unidirectional and high-density display of RBD. Both soluble recombinant RBD and RBD displayed on CLPs bind the ACE2 receptor with nanomolar affinity. Mice are vaccinated with soluble RBD or CLP-displayed RBD, formulated in Squalene-Water-Emulsion. The RBD-CLP vaccines induce higher levels of serum anti-spike antibodies than the soluble RBD vaccines. Remarkably, one injection with our lead RBD-CLP vaccine in mice elicits virus neutralization antibody titers comparable to those found in patients that had recovered from COVID-19. Following booster vaccinations, the virus neutralization titers exceed those measured after natural infection, at serum dilutions above 1:10,000. Thus, the RBD-CLP vaccine is a highly promising candidate for preventing COVID-19. |
format | Online Article Text |
id | pubmed-7804149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78041492021-01-21 Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity Fougeroux, Cyrielle Goksøyr, Louise Idorn, Manja Soroka, Vladislav Myeni, Sebenzile K. Dagil, Robert Janitzek, Christoph M. Søgaard, Max Aves, Kara-Lee Horsted, Emma W. Erdoğan, Sayit Mahmut Gustavsson, Tobias Dorosz, Jerzy Clemmensen, Stine Fredsgaard, Laurits Thrane, Susan Vidal-Calvo, Elena E. Khalifé, Paul Hulen, Thomas M. Choudhary, Swati Theisen, Michael Singh, Susheel K. Garcia-Senosiain, Asier Van Oosten, Linda Pijlman, Gorben Hierzberger, Bettina Domeyer, Tanja Nalewajek, Blanka W. Strøbæk, Anette Skrzypczak, Magdalena Andersson, Laura F. Buus, Søren Buus, Anette Stryhn Christensen, Jan Pravsgaard Dalebout, Tim J. Iversen, Kasper Harritshøj, Lene H. Mordmüller, Benjamin Ullum, Henrik Reinert, Line S. de Jongh, Willem Adriaan Kikkert, Marjolein Paludan, Søren R. Theander, Thor G. Nielsen, Morten A. Salanti, Ali Sander, Adam F. Nat Commun Article The rapid development of a SARS-CoV-2 vaccine is a global priority. Here, we develop two capsid-like particle (CLP)-based vaccines displaying the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein. RBD antigens are displayed on AP205 CLPs through a split-protein Tag/Catcher, ensuring unidirectional and high-density display of RBD. Both soluble recombinant RBD and RBD displayed on CLPs bind the ACE2 receptor with nanomolar affinity. Mice are vaccinated with soluble RBD or CLP-displayed RBD, formulated in Squalene-Water-Emulsion. The RBD-CLP vaccines induce higher levels of serum anti-spike antibodies than the soluble RBD vaccines. Remarkably, one injection with our lead RBD-CLP vaccine in mice elicits virus neutralization antibody titers comparable to those found in patients that had recovered from COVID-19. Following booster vaccinations, the virus neutralization titers exceed those measured after natural infection, at serum dilutions above 1:10,000. Thus, the RBD-CLP vaccine is a highly promising candidate for preventing COVID-19. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804149/ /pubmed/33436573 http://dx.doi.org/10.1038/s41467-020-20251-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fougeroux, Cyrielle Goksøyr, Louise Idorn, Manja Soroka, Vladislav Myeni, Sebenzile K. Dagil, Robert Janitzek, Christoph M. Søgaard, Max Aves, Kara-Lee Horsted, Emma W. Erdoğan, Sayit Mahmut Gustavsson, Tobias Dorosz, Jerzy Clemmensen, Stine Fredsgaard, Laurits Thrane, Susan Vidal-Calvo, Elena E. Khalifé, Paul Hulen, Thomas M. Choudhary, Swati Theisen, Michael Singh, Susheel K. Garcia-Senosiain, Asier Van Oosten, Linda Pijlman, Gorben Hierzberger, Bettina Domeyer, Tanja Nalewajek, Blanka W. Strøbæk, Anette Skrzypczak, Magdalena Andersson, Laura F. Buus, Søren Buus, Anette Stryhn Christensen, Jan Pravsgaard Dalebout, Tim J. Iversen, Kasper Harritshøj, Lene H. Mordmüller, Benjamin Ullum, Henrik Reinert, Line S. de Jongh, Willem Adriaan Kikkert, Marjolein Paludan, Søren R. Theander, Thor G. Nielsen, Morten A. Salanti, Ali Sander, Adam F. Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title | Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title_full | Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title_fullStr | Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title_full_unstemmed | Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title_short | Capsid-like particles decorated with the SARS-CoV-2 receptor-binding domain elicit strong virus neutralization activity |
title_sort | capsid-like particles decorated with the sars-cov-2 receptor-binding domain elicit strong virus neutralization activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804149/ https://www.ncbi.nlm.nih.gov/pubmed/33436573 http://dx.doi.org/10.1038/s41467-020-20251-8 |
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