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dc.contributor.authorSvindland, Signe C
dc.contributor.authorPedersen, Gabriel K
dc.contributor.authorPathirana, Rishi D
dc.contributor.authorBredholt, Geir
dc.contributor.authorNøstbakken, Jane K
dc.contributor.authorJul-Larsen, Åsne
dc.contributor.authorGuzmán, Carlos A
dc.contributor.authorMontomoli, Emanuele
dc.contributor.authorLapini, Giulia
dc.contributor.authorPiccirella, Simona
dc.contributor.authorJabbal-Gill, Inderjit
dc.contributor.authorHinchcliffe, Michael
dc.contributor.authorCox, Rebecca J
dc.date.accessioned2014-01-14T15:11:57Z
dc.date.available2014-01-14T15:11:57Z
dc.date.issued2013-11
dc.identifier.citationA study of Chitosan and c-di-GMP as mucosal adjuvants for intranasal influenza H5N1 vaccine. 2013, 7 (6):1181-93 Influenza Other Respir Virusesen
dc.identifier.issn1750-2659
dc.identifier.pmid23170900
dc.identifier.doi10.1111/irv.12056
dc.identifier.urihttp://hdl.handle.net/10033/311297
dc.description.abstractHighly pathogenic avian influenza A/H5N1 virus remains a potential pandemic threat, and it is essential to continue vaccine development against this subtype. A local mucosal immune response in the upper respiratory tract may stop influenza transmission. It is therefore important to develop effective intranasal pandemic influenza vaccines that induce mucosal immunity at the site of viral entry.
dc.language.isoenen
dc.rightsArchived with thanks to Influenza and other respiratory virusesen
dc.titleA study of Chitosan and c-di-GMP as mucosal adjuvants for intranasal influenza H5N1 vaccine.en
dc.typeArticleen
dc.contributor.departmentdepartment of vaccinology and applied microbiology, Helmholtz Centre for infection research, D38124 Braunschweig, Germanyen
dc.identifier.journalInfluenza and other respiratory virusesen
refterms.dateFOA2018-06-12T22:45:20Z
html.description.abstractHighly pathogenic avian influenza A/H5N1 virus remains a potential pandemic threat, and it is essential to continue vaccine development against this subtype. A local mucosal immune response in the upper respiratory tract may stop influenza transmission. It is therefore important to develop effective intranasal pandemic influenza vaccines that induce mucosal immunity at the site of viral entry.


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