Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.

BACKGROUND: Influenza A (flu) virus causes significant morbidity and mortality worldwide, and current vaccines require annual updating to protect against the rapidly arising antigenic variations due to antigenic shift and drift. In fact, current subunit or split flu vaccines rely exclusively on anti...

Full description

Bibliographic Details
Main Authors: Mohammed Alsharifi, Yoichi Furuya, Timothy R Bowden, Mario Lobigs, Aulikki Koskinen, Matthias Regner, Lee Trinidad, David B Boyle, Arno Müllbacher
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2671162?pdf=render
id doaj-d7df0ff886154443a74a919693951cdf
record_format Article
spelling doaj-d7df0ff886154443a74a919693951cdf2020-11-24T21:55:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0144e533610.1371/journal.pone.0005336Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.Mohammed AlsharifiYoichi FuruyaTimothy R BowdenMario LobigsAulikki KoskinenMatthias RegnerLee TrinidadDavid B BoyleArno MüllbacherBACKGROUND: Influenza A (flu) virus causes significant morbidity and mortality worldwide, and current vaccines require annual updating to protect against the rapidly arising antigenic variations due to antigenic shift and drift. In fact, current subunit or split flu vaccines rely exclusively on antibody responses for protection and do not induce cytotoxic T (Tc) cell responses, which are broadly cross-reactive between virus strains. We have previously reported that gamma-ray inactivated flu virus can induce cross-reactive Tc cell responses. METHODOLOGY/PRINCIPAL FINDING: Here, we report that intranasal administration of purified gamma-ray inactivated human influenza A virus preparations (gamma-Flu) effectively induces heterotypic and cross-protective immunity. A single intranasal administration of gamma-A/PR8[H1N1] protects mice against lethal H5N1 and other heterotypic infections. CONCLUSIONS/SIGNIFICANCE: Intranasal gamma-Flu represents a unique approach for a cross-protective vaccine against both seasonal as well as possible future pandemic influenza A virus infections.http://europepmc.org/articles/PMC2671162?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mohammed Alsharifi
Yoichi Furuya
Timothy R Bowden
Mario Lobigs
Aulikki Koskinen
Matthias Regner
Lee Trinidad
David B Boyle
Arno Müllbacher
spellingShingle Mohammed Alsharifi
Yoichi Furuya
Timothy R Bowden
Mario Lobigs
Aulikki Koskinen
Matthias Regner
Lee Trinidad
David B Boyle
Arno Müllbacher
Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
PLoS ONE
author_facet Mohammed Alsharifi
Yoichi Furuya
Timothy R Bowden
Mario Lobigs
Aulikki Koskinen
Matthias Regner
Lee Trinidad
David B Boyle
Arno Müllbacher
author_sort Mohammed Alsharifi
title Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
title_short Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
title_full Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
title_fullStr Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
title_full_unstemmed Intranasal flu vaccine protective against seasonal and H5N1 avian influenza infections.
title_sort intranasal flu vaccine protective against seasonal and h5n1 avian influenza infections.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description BACKGROUND: Influenza A (flu) virus causes significant morbidity and mortality worldwide, and current vaccines require annual updating to protect against the rapidly arising antigenic variations due to antigenic shift and drift. In fact, current subunit or split flu vaccines rely exclusively on antibody responses for protection and do not induce cytotoxic T (Tc) cell responses, which are broadly cross-reactive between virus strains. We have previously reported that gamma-ray inactivated flu virus can induce cross-reactive Tc cell responses. METHODOLOGY/PRINCIPAL FINDING: Here, we report that intranasal administration of purified gamma-ray inactivated human influenza A virus preparations (gamma-Flu) effectively induces heterotypic and cross-protective immunity. A single intranasal administration of gamma-A/PR8[H1N1] protects mice against lethal H5N1 and other heterotypic infections. CONCLUSIONS/SIGNIFICANCE: Intranasal gamma-Flu represents a unique approach for a cross-protective vaccine against both seasonal as well as possible future pandemic influenza A virus infections.
url http://europepmc.org/articles/PMC2671162?pdf=render
work_keys_str_mv AT mohammedalsharifi intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT yoichifuruya intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT timothyrbowden intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT mariolobigs intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT aulikkikoskinen intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT matthiasregner intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT leetrinidad intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT davidbboyle intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
AT arnomullbacher intranasalfluvaccineprotectiveagainstseasonalandh5n1avianinfluenzainfections
_version_ 1725862087481098240