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An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity
We evaluated enveloped virus-like particles (eVLPs) expressing various forms of the Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike protein and several adjuvants in an effort to identify a highly potent Coronavirus disease 2019 (COVID-19) vaccine candidate. eVLPs expressing a modi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282453/ https://www.ncbi.nlm.nih.gov/pubmed/34304928 http://dx.doi.org/10.1016/j.vaccine.2021.07.034 |
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author | Fluckiger, Anne-Catherine Ontsouka, Barthelemy Bozic, Jasminka Diress, Abebaw Ahmed, Tanvir Berthoud, Tamara Tran, Anh Duque, Diane Liao, Mingmin McCluskie, Michael Diaz-Mitoma, Francisco Anderson, David E. Soare, Catalina |
author_facet | Fluckiger, Anne-Catherine Ontsouka, Barthelemy Bozic, Jasminka Diress, Abebaw Ahmed, Tanvir Berthoud, Tamara Tran, Anh Duque, Diane Liao, Mingmin McCluskie, Michael Diaz-Mitoma, Francisco Anderson, David E. Soare, Catalina |
author_sort | Fluckiger, Anne-Catherine |
collection | PubMed |
description | We evaluated enveloped virus-like particles (eVLPs) expressing various forms of the Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike protein and several adjuvants in an effort to identify a highly potent Coronavirus disease 2019 (COVID-19) vaccine candidate. eVLPs expressing a modified prefusion form of SARS-CoV-2 spike protein were selected as they induced high antibody binding titers and neutralizing activity after a single injection in mice. Formulation of SARS-CoV-2 S eVLPs with aluminum phosphate resulted in balanced induction of IgG2 and IgG1 isotypes and antibody binding and neutralization titers were undiminished for more than 3 months after a single immunization. A single dose of this candidate, named VBI-2902a, protected Syrian golden hamsters from challenge with SARS-CoV-2 and supports the on-going clinical evaluation of VBI-2902a as a highly potent vaccine against COVID-19. |
format | Online Article Text |
id | pubmed-8282453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Authors. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82824532021-07-20 An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity Fluckiger, Anne-Catherine Ontsouka, Barthelemy Bozic, Jasminka Diress, Abebaw Ahmed, Tanvir Berthoud, Tamara Tran, Anh Duque, Diane Liao, Mingmin McCluskie, Michael Diaz-Mitoma, Francisco Anderson, David E. Soare, Catalina Vaccine Article We evaluated enveloped virus-like particles (eVLPs) expressing various forms of the Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike protein and several adjuvants in an effort to identify a highly potent Coronavirus disease 2019 (COVID-19) vaccine candidate. eVLPs expressing a modified prefusion form of SARS-CoV-2 spike protein were selected as they induced high antibody binding titers and neutralizing activity after a single injection in mice. Formulation of SARS-CoV-2 S eVLPs with aluminum phosphate resulted in balanced induction of IgG2 and IgG1 isotypes and antibody binding and neutralization titers were undiminished for more than 3 months after a single immunization. A single dose of this candidate, named VBI-2902a, protected Syrian golden hamsters from challenge with SARS-CoV-2 and supports the on-going clinical evaluation of VBI-2902a as a highly potent vaccine against COVID-19. The Authors. Published by Elsevier Ltd. 2021-08-16 2021-07-16 /pmc/articles/PMC8282453/ /pubmed/34304928 http://dx.doi.org/10.1016/j.vaccine.2021.07.034 Text en © 2021 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Fluckiger, Anne-Catherine Ontsouka, Barthelemy Bozic, Jasminka Diress, Abebaw Ahmed, Tanvir Berthoud, Tamara Tran, Anh Duque, Diane Liao, Mingmin McCluskie, Michael Diaz-Mitoma, Francisco Anderson, David E. Soare, Catalina An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title | An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title_full | An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title_fullStr | An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title_full_unstemmed | An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title_short | An enveloped virus-like particle vaccine expressing a stabilized prefusion form of the SARS-CoV-2 spike protein elicits highly potent immunity |
title_sort | enveloped virus-like particle vaccine expressing a stabilized prefusion form of the sars-cov-2 spike protein elicits highly potent immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282453/ https://www.ncbi.nlm.nih.gov/pubmed/34304928 http://dx.doi.org/10.1016/j.vaccine.2021.07.034 |
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