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Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines
Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has led to an unprecedented global health crisis, resulting in a critical need for effective vaccines that generate protective antibodies. Protein subunit vaccines represent a promising approach but often lack the immunogenicity required f...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209904/ https://www.ncbi.nlm.nih.gov/pubmed/34580619 http://dx.doi.org/10.1002/advs.202100316 |
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author | Colombani, Thibault Eggermont, Loek J. Rogers, Zachary J. McKay, Lindsay G. A. Avena, Laura E. Johnson, Rebecca I. Storm, Nadia Griffiths, Anthony Bencherif, Sidi A. |
author_facet | Colombani, Thibault Eggermont, Loek J. Rogers, Zachary J. McKay, Lindsay G. A. Avena, Laura E. Johnson, Rebecca I. Storm, Nadia Griffiths, Anthony Bencherif, Sidi A. |
author_sort | Colombani, Thibault |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has led to an unprecedented global health crisis, resulting in a critical need for effective vaccines that generate protective antibodies. Protein subunit vaccines represent a promising approach but often lack the immunogenicity required for strong immune stimulation. To overcome this challenge, it is first demonstrated that advanced biomaterials can be leveraged to boost the effectiveness of SARS‐CoV‐2 protein subunit vaccines. Additionally, it is reported that oxygen is a powerful immunological co‐adjuvant and has an ability to further potentiate vaccine potency. In preclinical studies, mice immunized with an oxygen‐generating coronavirus disease 2019 (COVID‐19) cryogel‐based vaccine (O(2)‐Cryogel(VAX)) exhibit a robust Th1 and Th2 immune response, leading to a sustained production of highly effective neutralizing antibodies against the virus. Even with a single immunization, O(2)‐Cryogel(VAX) achieves high antibody titers within 21 days, and both binding and neutralizing antibody levels are further increased after a second dose. Engineering a potent vaccine system that generates sufficient neutralizing antibodies after one dose is a preferred strategy amid vaccine shortage. The data suggest that this platform is a promising technology to reinforce vaccine‐driven immunostimulation and is applicable to current and emerging infectious diseases. |
format | Online Article Text |
id | pubmed-8209904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82099042021-06-21 Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines Colombani, Thibault Eggermont, Loek J. Rogers, Zachary J. McKay, Lindsay G. A. Avena, Laura E. Johnson, Rebecca I. Storm, Nadia Griffiths, Anthony Bencherif, Sidi A. Adv Sci (Weinh) Research Articles Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has led to an unprecedented global health crisis, resulting in a critical need for effective vaccines that generate protective antibodies. Protein subunit vaccines represent a promising approach but often lack the immunogenicity required for strong immune stimulation. To overcome this challenge, it is first demonstrated that advanced biomaterials can be leveraged to boost the effectiveness of SARS‐CoV‐2 protein subunit vaccines. Additionally, it is reported that oxygen is a powerful immunological co‐adjuvant and has an ability to further potentiate vaccine potency. In preclinical studies, mice immunized with an oxygen‐generating coronavirus disease 2019 (COVID‐19) cryogel‐based vaccine (O(2)‐Cryogel(VAX)) exhibit a robust Th1 and Th2 immune response, leading to a sustained production of highly effective neutralizing antibodies against the virus. Even with a single immunization, O(2)‐Cryogel(VAX) achieves high antibody titers within 21 days, and both binding and neutralizing antibody levels are further increased after a second dose. Engineering a potent vaccine system that generates sufficient neutralizing antibodies after one dose is a preferred strategy amid vaccine shortage. The data suggest that this platform is a promising technology to reinforce vaccine‐driven immunostimulation and is applicable to current and emerging infectious diseases. John Wiley and Sons Inc. 2021-07-20 /pmc/articles/PMC8209904/ /pubmed/34580619 http://dx.doi.org/10.1002/advs.202100316 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Colombani, Thibault Eggermont, Loek J. Rogers, Zachary J. McKay, Lindsay G. A. Avena, Laura E. Johnson, Rebecca I. Storm, Nadia Griffiths, Anthony Bencherif, Sidi A. Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title | Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title_full | Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title_fullStr | Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title_full_unstemmed | Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title_short | Biomaterials and Oxygen Join Forces to Shape the Immune Response and Boost COVID‐19 Vaccines |
title_sort | biomaterials and oxygen join forces to shape the immune response and boost covid‐19 vaccines |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209904/ https://www.ncbi.nlm.nih.gov/pubmed/34580619 http://dx.doi.org/10.1002/advs.202100316 |
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