Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages

Summary: A quarter of all seasonal influenza cases are caused by type B influenza virus (IBV) that also dominates periodically. Here, we investigated a recombinant adenovirus vaccine carrying a synthetic HA2 representing the consensus sequence of all IBV hemagglutinins. The vaccine fully protected m...

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Autores principales: Caroline Gravel, Abenaya Muralidharan, Amparo Duran, Adrian Zetner, Annabelle Pfeifle, Wanyue Zhang, Anwar Hashem, Levi Tamming, Aaron Farnsworth, Hugues Loemba, Wangxue Chen, Florian Krammer, David Safronetz, Jingxin Cao, Lisheng Wang, Simon Sauve, Michael Rosu-Myles, Gary Van Domselaar, Xuguang Li
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Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/c44338db000c4fca9f7baa27557288ba
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spelling oai:doaj.org-article:c44338db000c4fca9f7baa27557288ba2021-11-20T05:09:59ZSynthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages2589-004210.1016/j.isci.2021.103328https://doaj.org/article/c44338db000c4fca9f7baa27557288ba2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221012979https://doaj.org/toc/2589-0042Summary: A quarter of all seasonal influenza cases are caused by type B influenza virus (IBV) that also dominates periodically. Here, we investigated a recombinant adenovirus vaccine carrying a synthetic HA2 representing the consensus sequence of all IBV hemagglutinins. The vaccine fully protected mice from lethal challenges by IBV of both genetic lineages, demonstrating its breadth of protection. The protection was not mediated by neutralizing antibodies but robust antibody-dependent cellular cytotoxicity and cell-mediated immune responses. Complete protection of the animals required the entire codon-optimized HA2 sequence that elicited a balanced immune response, whereas truncated vaccines without either the fusion peptide or the transmembrane domain reduced the efficacy of protection. Finally, the vaccines did not demonstrate any sign of disease exacerbation following lung pathology and morbidity monitoring. Collectively, these data suggest that it could be worth further exploring this prototype universal vaccine because of its considerable efficacy, safety, and breadth of protection.Caroline GravelAbenaya MuralidharanAmparo DuranAdrian ZetnerAnnabelle PfeifleWanyue ZhangAnwar HashemLevi TammingAaron FarnsworthHugues LoembaWangxue ChenFlorian KrammerDavid SafronetzJingxin CaoLisheng WangSimon SauveMichael Rosu-MylesGary Van DomselaarXuguang LiElsevierarticleImmunologyimmune responseVirologyScienceQENiScience, Vol 24, Iss 11, Pp 103328- (2021)
institution DOAJ
collection DOAJ
language EN
topic Immunology
immune response
Virology
Science
Q
spellingShingle Immunology
immune response
Virology
Science
Q
Caroline Gravel
Abenaya Muralidharan
Amparo Duran
Adrian Zetner
Annabelle Pfeifle
Wanyue Zhang
Anwar Hashem
Levi Tamming
Aaron Farnsworth
Hugues Loemba
Wangxue Chen
Florian Krammer
David Safronetz
Jingxin Cao
Lisheng Wang
Simon Sauve
Michael Rosu-Myles
Gary Van Domselaar
Xuguang Li
Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
description Summary: A quarter of all seasonal influenza cases are caused by type B influenza virus (IBV) that also dominates periodically. Here, we investigated a recombinant adenovirus vaccine carrying a synthetic HA2 representing the consensus sequence of all IBV hemagglutinins. The vaccine fully protected mice from lethal challenges by IBV of both genetic lineages, demonstrating its breadth of protection. The protection was not mediated by neutralizing antibodies but robust antibody-dependent cellular cytotoxicity and cell-mediated immune responses. Complete protection of the animals required the entire codon-optimized HA2 sequence that elicited a balanced immune response, whereas truncated vaccines without either the fusion peptide or the transmembrane domain reduced the efficacy of protection. Finally, the vaccines did not demonstrate any sign of disease exacerbation following lung pathology and morbidity monitoring. Collectively, these data suggest that it could be worth further exploring this prototype universal vaccine because of its considerable efficacy, safety, and breadth of protection.
format article
author Caroline Gravel
Abenaya Muralidharan
Amparo Duran
Adrian Zetner
Annabelle Pfeifle
Wanyue Zhang
Anwar Hashem
Levi Tamming
Aaron Farnsworth
Hugues Loemba
Wangxue Chen
Florian Krammer
David Safronetz
Jingxin Cao
Lisheng Wang
Simon Sauve
Michael Rosu-Myles
Gary Van Domselaar
Xuguang Li
author_facet Caroline Gravel
Abenaya Muralidharan
Amparo Duran
Adrian Zetner
Annabelle Pfeifle
Wanyue Zhang
Anwar Hashem
Levi Tamming
Aaron Farnsworth
Hugues Loemba
Wangxue Chen
Florian Krammer
David Safronetz
Jingxin Cao
Lisheng Wang
Simon Sauve
Michael Rosu-Myles
Gary Van Domselaar
Xuguang Li
author_sort Caroline Gravel
title Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
title_short Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
title_full Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
title_fullStr Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
title_full_unstemmed Synthetic vaccine affords full protection to mice against lethal challenge of influenza B virus of both genetic lineages
title_sort synthetic vaccine affords full protection to mice against lethal challenge of influenza b virus of both genetic lineages
publisher Elsevier
publishDate 2021
url https://doaj.org/article/c44338db000c4fca9f7baa27557288ba
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