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Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model
Epidemic or pandemic influenza can annually cause significant morbidity and mortality in humans. We developed novel chimeric hemagglutinin (cHA)-based universal influenza virus vaccines, which contain a conserved HA stalk domain from a 2009 pandemic H1N1 (pH1N1) strain combined with globular head do...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826668/ https://www.ncbi.nlm.nih.gov/pubmed/33440898 http://dx.doi.org/10.3390/vaccines9010040 |
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author | Liu, Wen-Chun Nachbagauer, Raffael Stadlbauer, Daniel Strohmeier, Shirin Solórzano, Alicia Berlanda-Scorza, Francesco Innis, Bruce L. García-Sastre, Adolfo Palese, Peter Krammer, Florian Albrecht, Randy A. |
author_facet | Liu, Wen-Chun Nachbagauer, Raffael Stadlbauer, Daniel Strohmeier, Shirin Solórzano, Alicia Berlanda-Scorza, Francesco Innis, Bruce L. García-Sastre, Adolfo Palese, Peter Krammer, Florian Albrecht, Randy A. |
author_sort | Liu, Wen-Chun |
collection | PubMed |
description | Epidemic or pandemic influenza can annually cause significant morbidity and mortality in humans. We developed novel chimeric hemagglutinin (cHA)-based universal influenza virus vaccines, which contain a conserved HA stalk domain from a 2009 pandemic H1N1 (pH1N1) strain combined with globular head domains from avian influenza A viruses. Our previous reports demonstrated that prime-boost sequential immunizations induced robust antibody responses directed toward the conserved HA stalk domain in ferrets. Herein, we further followed vaccinated animals for one year to compare the efficacy and durability of these vaccines in the preclinical ferret model of influenza. Although all cHA-based immunization regimens induced durable HA stalk-specific and heterosubtypic antibody responses in ferrets, sequential immunization with live-attenuated influenza virus vaccines (LAIV-LAIV) conferred the best protection against upper respiratory tract infection by a pH1N1 influenza A virus. The findings from this study suggest that our sequential immunization strategy for a cHA-based universal influenza virus vaccine provides durable protective humoral and cellular immunity against influenza virus infection. |
format | Online Article Text |
id | pubmed-7826668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78266682021-01-25 Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model Liu, Wen-Chun Nachbagauer, Raffael Stadlbauer, Daniel Strohmeier, Shirin Solórzano, Alicia Berlanda-Scorza, Francesco Innis, Bruce L. García-Sastre, Adolfo Palese, Peter Krammer, Florian Albrecht, Randy A. Vaccines (Basel) Article Epidemic or pandemic influenza can annually cause significant morbidity and mortality in humans. We developed novel chimeric hemagglutinin (cHA)-based universal influenza virus vaccines, which contain a conserved HA stalk domain from a 2009 pandemic H1N1 (pH1N1) strain combined with globular head domains from avian influenza A viruses. Our previous reports demonstrated that prime-boost sequential immunizations induced robust antibody responses directed toward the conserved HA stalk domain in ferrets. Herein, we further followed vaccinated animals for one year to compare the efficacy and durability of these vaccines in the preclinical ferret model of influenza. Although all cHA-based immunization regimens induced durable HA stalk-specific and heterosubtypic antibody responses in ferrets, sequential immunization with live-attenuated influenza virus vaccines (LAIV-LAIV) conferred the best protection against upper respiratory tract infection by a pH1N1 influenza A virus. The findings from this study suggest that our sequential immunization strategy for a cHA-based universal influenza virus vaccine provides durable protective humoral and cellular immunity against influenza virus infection. MDPI 2021-01-11 /pmc/articles/PMC7826668/ /pubmed/33440898 http://dx.doi.org/10.3390/vaccines9010040 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Wen-Chun Nachbagauer, Raffael Stadlbauer, Daniel Strohmeier, Shirin Solórzano, Alicia Berlanda-Scorza, Francesco Innis, Bruce L. García-Sastre, Adolfo Palese, Peter Krammer, Florian Albrecht, Randy A. Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title | Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title_full | Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title_fullStr | Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title_full_unstemmed | Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title_short | Chimeric Hemagglutinin-Based Live-Attenuated Vaccines Confer Durable Protective Immunity against Influenza A Viruses in a Preclinical Ferret Model |
title_sort | chimeric hemagglutinin-based live-attenuated vaccines confer durable protective immunity against influenza a viruses in a preclinical ferret model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826668/ https://www.ncbi.nlm.nih.gov/pubmed/33440898 http://dx.doi.org/10.3390/vaccines9010040 |
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