Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice

The need for more effective influenza vaccines is highlighted by the emergence of novel influenza strains, which can lead to new pandemics. There is a growing population of susceptible subjects at risk for severe complications of influenza, such as the elderly who are only in part protected by curre...

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Main Authors: Thomas Ebensen, Jennifer Debarry, Gabriel K. Pedersen, Paulina Blazejewska, Sebastian Weissmann, Kai Schulze, Kenneth C. McCullough, Rebecca J. Cox, Carlos A. Guzmán
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-09-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.01223/full
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spelling doaj-823265d357f44f59aa1a3b2f3b294ace2020-11-24T22:29:49ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-09-01810.3389/fimmu.2017.01223289805Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in MiceThomas Ebensen0Jennifer Debarry1Gabriel K. Pedersen2Gabriel K. Pedersen3Gabriel K. Pedersen4Paulina Blazejewska5Sebastian Weissmann6Kai Schulze7Kenneth C. McCullough8Rebecca J. Cox9Rebecca J. Cox10Rebecca J. Cox11Carlos A. Guzmán12Department of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyThe Influenza Centre, University of Bergen, Bergen, NorwayJebsen Centre for Influenza Vaccine Research, Department of Clinical Science, University of Bergen, Bergen, NorwayDepartment of Research and Development, Haukeland University Hospital, Bergen, NorwayDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyInstitute of Virology and Immunology, Mittelhäusern, SwitzerlandThe Influenza Centre, University of Bergen, Bergen, NorwayJebsen Centre for Influenza Vaccine Research, Department of Clinical Science, University of Bergen, Bergen, NorwayDepartment of Research and Development, Haukeland University Hospital, Bergen, NorwayDepartment of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, Braunschweig, GermanyThe need for more effective influenza vaccines is highlighted by the emergence of novel influenza strains, which can lead to new pandemics. There is a growing population of susceptible subjects at risk for severe complications of influenza, such as the elderly who are only in part protected by current licensed seasonal vaccines. One strategy for improving seasonal and pandemic vaccines takes advantage of adjuvants to boost and modulate evoked immune responses. In this study, we examined the capacity of the recently described adjuvant cyclic di-adenosine monophosphate (c-di-AMP) to serve as an adjuvant for improved mucosal influenza vaccines, and induce effective protection against influenza H5N1. In detail, c-di-AMP promoted (i) effective local and systemic humoral immune responses, including protective hemagglutination inhibition titers, (ii) effective cellular responses, including multifunctional T cell activity, (iii) induction of long-lasting immunity, and (iv) protection against viral challenge. Furthermore, we demonstrated the dose-sparing capacity of the adjuvant as well as the ability to evoke cross-clade protective immune responses. Overall, our results suggest that c-di-AMP contributes to the generation of a protective cell-mediated immune response required for efficacious vaccination against influenza, which supports the further development of c-di-AMP as an adjuvant for seasonal and pandemic influenza mucosal vaccines.http://journal.frontiersin.org/article/10.3389/fimmu.2017.01223/fullmucosal adjuvantcyclic di-adenosine monophosphatesublingual administrationc-di-GMPdose-sparing capacity
collection DOAJ
language English
format Article
sources DOAJ
author Thomas Ebensen
Jennifer Debarry
Gabriel K. Pedersen
Gabriel K. Pedersen
Gabriel K. Pedersen
Paulina Blazejewska
Sebastian Weissmann
Kai Schulze
Kenneth C. McCullough
Rebecca J. Cox
Rebecca J. Cox
Rebecca J. Cox
Carlos A. Guzmán
spellingShingle Thomas Ebensen
Jennifer Debarry
Gabriel K. Pedersen
Gabriel K. Pedersen
Gabriel K. Pedersen
Paulina Blazejewska
Sebastian Weissmann
Kai Schulze
Kenneth C. McCullough
Rebecca J. Cox
Rebecca J. Cox
Rebecca J. Cox
Carlos A. Guzmán
Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
Frontiers in Immunology
mucosal adjuvant
cyclic di-adenosine monophosphate
sublingual administration
c-di-GMP
dose-sparing capacity
author_facet Thomas Ebensen
Jennifer Debarry
Gabriel K. Pedersen
Gabriel K. Pedersen
Gabriel K. Pedersen
Paulina Blazejewska
Sebastian Weissmann
Kai Schulze
Kenneth C. McCullough
Rebecca J. Cox
Rebecca J. Cox
Rebecca J. Cox
Carlos A. Guzmán
author_sort Thomas Ebensen
title Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
title_short Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
title_full Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
title_fullStr Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
title_full_unstemmed Mucosal Administration of Cycle-Di-Nucleotide-Adjuvanted Virosomes Efficiently Induces Protection against Influenza H5N1 in Mice
title_sort mucosal administration of cycle-di-nucleotide-adjuvanted virosomes efficiently induces protection against influenza h5n1 in mice
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2017-09-01
description The need for more effective influenza vaccines is highlighted by the emergence of novel influenza strains, which can lead to new pandemics. There is a growing population of susceptible subjects at risk for severe complications of influenza, such as the elderly who are only in part protected by current licensed seasonal vaccines. One strategy for improving seasonal and pandemic vaccines takes advantage of adjuvants to boost and modulate evoked immune responses. In this study, we examined the capacity of the recently described adjuvant cyclic di-adenosine monophosphate (c-di-AMP) to serve as an adjuvant for improved mucosal influenza vaccines, and induce effective protection against influenza H5N1. In detail, c-di-AMP promoted (i) effective local and systemic humoral immune responses, including protective hemagglutination inhibition titers, (ii) effective cellular responses, including multifunctional T cell activity, (iii) induction of long-lasting immunity, and (iv) protection against viral challenge. Furthermore, we demonstrated the dose-sparing capacity of the adjuvant as well as the ability to evoke cross-clade protective immune responses. Overall, our results suggest that c-di-AMP contributes to the generation of a protective cell-mediated immune response required for efficacious vaccination against influenza, which supports the further development of c-di-AMP as an adjuvant for seasonal and pandemic influenza mucosal vaccines.
topic mucosal adjuvant
cyclic di-adenosine monophosphate
sublingual administration
c-di-GMP
dose-sparing capacity
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.01223/full
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