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Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters

Vaccines play a critical role in combating the COVID-19 pandemic. Future control of the pandemic requires improved vaccines with high efficacy against newly emerging SARS-CoV-2 variants and the ability to reduce virus transmission. Here we compare immune responses and preclinical efficacy of the mRN...

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Autores principales: Nouailles, Geraldine, Adler, Julia M., Pennitz, Peter, Peidli, Stefan, Teixeira Alves, Luiz Gustavo, Baumgardt, Morris, Bushe, Judith, Voss, Anne, Langenhagen, Alina, Langner, Christine, Martin Vidal, Ricardo, Pott, Fabian, Kazmierski, Julia, Ebenig, Aileen, Lange, Mona V., Mühlebach, Michael D., Goekeri, Cengiz, Simmons, Szandor, Xing, Na, Abdelgawad, Azza, Herwig, Susanne, Cichon, Günter, Niemeyer, Daniela, Drosten, Christian, Goffinet, Christine, Landthaler, Markus, Blüthgen, Nils, Wu, Haibo, Witzenrath, Martin, Gruber, Achim D., Praktiknjo, Samantha D., Osterrieder, Nikolaus, Wyler, Emanuel, Kunec, Dusan, Trimpert, Jakob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159847/
https://www.ncbi.nlm.nih.gov/pubmed/37012419
http://dx.doi.org/10.1038/s41564-023-01352-8
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author Nouailles, Geraldine
Adler, Julia M.
Pennitz, Peter
Peidli, Stefan
Teixeira Alves, Luiz Gustavo
Baumgardt, Morris
Bushe, Judith
Voss, Anne
Langenhagen, Alina
Langner, Christine
Martin Vidal, Ricardo
Pott, Fabian
Kazmierski, Julia
Ebenig, Aileen
Lange, Mona V.
Mühlebach, Michael D.
Goekeri, Cengiz
Simmons, Szandor
Xing, Na
Abdelgawad, Azza
Herwig, Susanne
Cichon, Günter
Niemeyer, Daniela
Drosten, Christian
Goffinet, Christine
Landthaler, Markus
Blüthgen, Nils
Wu, Haibo
Witzenrath, Martin
Gruber, Achim D.
Praktiknjo, Samantha D.
Osterrieder, Nikolaus
Wyler, Emanuel
Kunec, Dusan
Trimpert, Jakob
author_facet Nouailles, Geraldine
Adler, Julia M.
Pennitz, Peter
Peidli, Stefan
Teixeira Alves, Luiz Gustavo
Baumgardt, Morris
Bushe, Judith
Voss, Anne
Langenhagen, Alina
Langner, Christine
Martin Vidal, Ricardo
Pott, Fabian
Kazmierski, Julia
Ebenig, Aileen
Lange, Mona V.
Mühlebach, Michael D.
Goekeri, Cengiz
Simmons, Szandor
Xing, Na
Abdelgawad, Azza
Herwig, Susanne
Cichon, Günter
Niemeyer, Daniela
Drosten, Christian
Goffinet, Christine
Landthaler, Markus
Blüthgen, Nils
Wu, Haibo
Witzenrath, Martin
Gruber, Achim D.
Praktiknjo, Samantha D.
Osterrieder, Nikolaus
Wyler, Emanuel
Kunec, Dusan
Trimpert, Jakob
author_sort Nouailles, Geraldine
collection PubMed
description Vaccines play a critical role in combating the COVID-19 pandemic. Future control of the pandemic requires improved vaccines with high efficacy against newly emerging SARS-CoV-2 variants and the ability to reduce virus transmission. Here we compare immune responses and preclinical efficacy of the mRNA vaccine BNT162b2, the adenovirus-vectored spike vaccine Ad2-spike and the live-attenuated virus vaccine candidate sCPD9 in Syrian hamsters, using both homogeneous and heterologous vaccination regimens. Comparative vaccine efficacy was assessed by employing readouts from virus titrations to single-cell RNA sequencing. Our results show that sCPD9 vaccination elicited the most robust immunity, including rapid viral clearance, reduced tissue damage, fast differentiation of pre-plasmablasts, strong systemic and mucosal humoral responses, and rapid recall of memory T cells from lung tissue after challenge with heterologous SARS-CoV-2. Overall, our results demonstrate that live-attenuated vaccines offer advantages over currently available COVID-19 vaccines.
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spelling pubmed-101598472023-05-06 Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters Nouailles, Geraldine Adler, Julia M. Pennitz, Peter Peidli, Stefan Teixeira Alves, Luiz Gustavo Baumgardt, Morris Bushe, Judith Voss, Anne Langenhagen, Alina Langner, Christine Martin Vidal, Ricardo Pott, Fabian Kazmierski, Julia Ebenig, Aileen Lange, Mona V. Mühlebach, Michael D. Goekeri, Cengiz Simmons, Szandor Xing, Na Abdelgawad, Azza Herwig, Susanne Cichon, Günter Niemeyer, Daniela Drosten, Christian Goffinet, Christine Landthaler, Markus Blüthgen, Nils Wu, Haibo Witzenrath, Martin Gruber, Achim D. Praktiknjo, Samantha D. Osterrieder, Nikolaus Wyler, Emanuel Kunec, Dusan Trimpert, Jakob Nat Microbiol Article Vaccines play a critical role in combating the COVID-19 pandemic. Future control of the pandemic requires improved vaccines with high efficacy against newly emerging SARS-CoV-2 variants and the ability to reduce virus transmission. Here we compare immune responses and preclinical efficacy of the mRNA vaccine BNT162b2, the adenovirus-vectored spike vaccine Ad2-spike and the live-attenuated virus vaccine candidate sCPD9 in Syrian hamsters, using both homogeneous and heterologous vaccination regimens. Comparative vaccine efficacy was assessed by employing readouts from virus titrations to single-cell RNA sequencing. Our results show that sCPD9 vaccination elicited the most robust immunity, including rapid viral clearance, reduced tissue damage, fast differentiation of pre-plasmablasts, strong systemic and mucosal humoral responses, and rapid recall of memory T cells from lung tissue after challenge with heterologous SARS-CoV-2. Overall, our results demonstrate that live-attenuated vaccines offer advantages over currently available COVID-19 vaccines. Nature Publishing Group UK 2023-04-03 2023 /pmc/articles/PMC10159847/ /pubmed/37012419 http://dx.doi.org/10.1038/s41564-023-01352-8 Text en © The Author(s) 2023 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
Nouailles, Geraldine
Adler, Julia M.
Pennitz, Peter
Peidli, Stefan
Teixeira Alves, Luiz Gustavo
Baumgardt, Morris
Bushe, Judith
Voss, Anne
Langenhagen, Alina
Langner, Christine
Martin Vidal, Ricardo
Pott, Fabian
Kazmierski, Julia
Ebenig, Aileen
Lange, Mona V.
Mühlebach, Michael D.
Goekeri, Cengiz
Simmons, Szandor
Xing, Na
Abdelgawad, Azza
Herwig, Susanne
Cichon, Günter
Niemeyer, Daniela
Drosten, Christian
Goffinet, Christine
Landthaler, Markus
Blüthgen, Nils
Wu, Haibo
Witzenrath, Martin
Gruber, Achim D.
Praktiknjo, Samantha D.
Osterrieder, Nikolaus
Wyler, Emanuel
Kunec, Dusan
Trimpert, Jakob
Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title_full Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title_fullStr Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title_full_unstemmed Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title_short Live-attenuated vaccine sCPD9 elicits superior mucosal and systemic immunity to SARS-CoV-2 variants in hamsters
title_sort live-attenuated vaccine scpd9 elicits superior mucosal and systemic immunity to sars-cov-2 variants in hamsters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159847/
https://www.ncbi.nlm.nih.gov/pubmed/37012419
http://dx.doi.org/10.1038/s41564-023-01352-8
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