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Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity
The objective of this study is to further analyze recombinant rabies virus-vectored SARS-CoV-2 vaccine, CORAVAX, as an effective COVID-19 vaccine strategy. CORAVAX has proven immunogenic and protective against SARS-CoV-2 in animal models. Here, we have screened adjuvants for the highest quality anti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508099/ https://www.ncbi.nlm.nih.gov/pubmed/36151100 http://dx.doi.org/10.1038/s41541-022-00532-7 |
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author | Yankowski, Catherine Wirblich, Christoph Kurup, Drishya Schnell, Matthias J. |
author_facet | Yankowski, Catherine Wirblich, Christoph Kurup, Drishya Schnell, Matthias J. |
author_sort | Yankowski, Catherine |
collection | PubMed |
description | The objective of this study is to further analyze recombinant rabies virus-vectored SARS-CoV-2 vaccine, CORAVAX, as an effective COVID-19 vaccine strategy. CORAVAX has proven immunogenic and protective against SARS-CoV-2 in animal models. Here, we have screened adjuvants for the highest quality antibody titers, negated the concern of pre-existing rabies-vector immunity, and established its potential as a long-term COVID-19 vaccine. We have tested toll-like receptor 4 (TLR4) agonists, inflammasome activators, and alum adjuvants in CORAVAX and found TLR4-activating MPLA-AddaVax to have the greatest potential. We followed the humoral immune response to CORAVAX in mice with pre-existing rabies virus immunity and saw no significant differences compared to naive mice. We then followed the immune response to CORAVAX over several months and 1-year post-immunization. Mice maintained high antigen-specific serum antibody titers as well as long-lived antibody-secreting cells in the spleen and bone marrow. We believe this rabies-vector strategy combats the problem of waning immunity of other COVID-19 vaccines. These results together support CORAVAX’s potential during the ongoing COVID-19 pandemic. |
format | Online Article Text |
id | pubmed-9508099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95080992022-09-25 Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity Yankowski, Catherine Wirblich, Christoph Kurup, Drishya Schnell, Matthias J. NPJ Vaccines Article The objective of this study is to further analyze recombinant rabies virus-vectored SARS-CoV-2 vaccine, CORAVAX, as an effective COVID-19 vaccine strategy. CORAVAX has proven immunogenic and protective against SARS-CoV-2 in animal models. Here, we have screened adjuvants for the highest quality antibody titers, negated the concern of pre-existing rabies-vector immunity, and established its potential as a long-term COVID-19 vaccine. We have tested toll-like receptor 4 (TLR4) agonists, inflammasome activators, and alum adjuvants in CORAVAX and found TLR4-activating MPLA-AddaVax to have the greatest potential. We followed the humoral immune response to CORAVAX in mice with pre-existing rabies virus immunity and saw no significant differences compared to naive mice. We then followed the immune response to CORAVAX over several months and 1-year post-immunization. Mice maintained high antigen-specific serum antibody titers as well as long-lived antibody-secreting cells in the spleen and bone marrow. We believe this rabies-vector strategy combats the problem of waning immunity of other COVID-19 vaccines. These results together support CORAVAX’s potential during the ongoing COVID-19 pandemic. Nature Publishing Group UK 2022-09-23 /pmc/articles/PMC9508099/ /pubmed/36151100 http://dx.doi.org/10.1038/s41541-022-00532-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yankowski, Catherine Wirblich, Christoph Kurup, Drishya Schnell, Matthias J. Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title | Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title_full | Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title_fullStr | Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title_full_unstemmed | Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title_short | Inactivated rabies-vectored SARS-CoV-2 vaccine provides long-term immune response unaffected by vector immunity |
title_sort | inactivated rabies-vectored sars-cov-2 vaccine provides long-term immune response unaffected by vector immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508099/ https://www.ncbi.nlm.nih.gov/pubmed/36151100 http://dx.doi.org/10.1038/s41541-022-00532-7 |
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