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Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine
Vaccines that protect against any H1N1 influenza A virus strain would be advantageous for use in pigs and humans. Here, we try to induce a pan-H1N1 antibody response in pigs by sequential vaccination with antigenically divergent H1N1 strains. Adjuvanted whole inactivated vaccines are given intramusc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679120/ https://www.ncbi.nlm.nih.gov/pubmed/38008801 http://dx.doi.org/10.1038/s41467-023-43339-3 |
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author | Van Reeth, Kristien Parys, Anna Gracia, José Carlos Mancera Trus, Ivan Chiers, Koen Meade, Philip Liu, Sean Palese, Peter Krammer, Florian Vandoorn, Elien |
author_facet | Van Reeth, Kristien Parys, Anna Gracia, José Carlos Mancera Trus, Ivan Chiers, Koen Meade, Philip Liu, Sean Palese, Peter Krammer, Florian Vandoorn, Elien |
author_sort | Van Reeth, Kristien |
collection | PubMed |
description | Vaccines that protect against any H1N1 influenza A virus strain would be advantageous for use in pigs and humans. Here, we try to induce a pan-H1N1 antibody response in pigs by sequential vaccination with antigenically divergent H1N1 strains. Adjuvanted whole inactivated vaccines are given intramuscularly in various two- and three-dose regimens. Three doses of heterologous monovalent H1N1 vaccine result in seroprotective neutralizing antibodies against 71% of a diverse panel of human and swine H1 strains, detectable antibodies against 88% of strains, and sterile cross-clade immunity against two heterologous challenge strains. This strategy outperforms any two-dose regimen and is as good or better than giving three doses of matched trivalent vaccine. Neutralizing antibodies are H1-specific, and the second heterologous booster enhances reactivity with conserved epitopes in the HA head. We show that even the most traditional influenza vaccines can offer surprisingly broad protection if they are administered in an alternative way. |
format | Online Article Text |
id | pubmed-10679120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106791202023-11-27 Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine Van Reeth, Kristien Parys, Anna Gracia, José Carlos Mancera Trus, Ivan Chiers, Koen Meade, Philip Liu, Sean Palese, Peter Krammer, Florian Vandoorn, Elien Nat Commun Article Vaccines that protect against any H1N1 influenza A virus strain would be advantageous for use in pigs and humans. Here, we try to induce a pan-H1N1 antibody response in pigs by sequential vaccination with antigenically divergent H1N1 strains. Adjuvanted whole inactivated vaccines are given intramuscularly in various two- and three-dose regimens. Three doses of heterologous monovalent H1N1 vaccine result in seroprotective neutralizing antibodies against 71% of a diverse panel of human and swine H1 strains, detectable antibodies against 88% of strains, and sterile cross-clade immunity against two heterologous challenge strains. This strategy outperforms any two-dose regimen and is as good or better than giving three doses of matched trivalent vaccine. Neutralizing antibodies are H1-specific, and the second heterologous booster enhances reactivity with conserved epitopes in the HA head. We show that even the most traditional influenza vaccines can offer surprisingly broad protection if they are administered in an alternative way. Nature Publishing Group UK 2023-11-27 /pmc/articles/PMC10679120/ /pubmed/38008801 http://dx.doi.org/10.1038/s41467-023-43339-3 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Van Reeth, Kristien Parys, Anna Gracia, José Carlos Mancera Trus, Ivan Chiers, Koen Meade, Philip Liu, Sean Palese, Peter Krammer, Florian Vandoorn, Elien Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title | Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title_full | Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title_fullStr | Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title_full_unstemmed | Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title_short | Sequential vaccinations with divergent H1N1 influenza virus strains induce multi-H1 clade neutralizing antibodies in swine |
title_sort | sequential vaccinations with divergent h1n1 influenza virus strains induce multi-h1 clade neutralizing antibodies in swine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679120/ https://www.ncbi.nlm.nih.gov/pubmed/38008801 http://dx.doi.org/10.1038/s41467-023-43339-3 |
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