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Intranasal Flu Vaccine Protective against Seasonal and H5N1 Avian Influenza Infections
Author(s) -
Mohammed Alsharifi,
Yoichi Furuya,
Timothy R. Bowden,
Mario Lobigs,
Aulikki Koskinen,
Matthias Regner,
Lee Trinidad,
David B. Boyle,
Arno Müllbacher
Publication year - 2009
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0005336
Subject(s) - virology , nasal administration , virus , influenza a virus , influenza a virus subtype h5n1 , pandemic , antigenic drift , antigen , immunity , immunology , biology , vaccination , h5n1 genetic structure , orthomyxoviridae , medicine , antigenic shift , microbiology and biotechnology , immune system , covid-19 , infectious disease (medical specialty) , disease , pathology
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 γ-ray inactivated flu virus can induce cross-reactive Tc cell responses. Methodology/Principal Finding Here, we report that intranasal administration of purified γ-ray inactivated human influenza A virus preparations (γ-Flu) effectively induces heterotypic and cross-protective immunity. A single intranasal administration of γ-A/PR8[H1N1] protects mice against lethal H5N1 and other heterotypic infections. Conclusions/Significance Intranasal γ-Flu represents a unique approach for a cross-protective vaccine against both seasonal as well as possible future pandemic influenza A virus infections.

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