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cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model

Current strategies for improving protective response to influenza vaccines during immunosenescence do not adequately protect individuals over 65 years of age. Here, we used an aged mouse model to investigate the potential of co-delivery of influenza vaccine with the recently identified combination o...

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Autores principales: Vassilieva, Elena V., Li, Song, Korniychuk, Heorhiy, Taylor, Dahnide M., Wang, Shelly, Prausnitz, Mark R., Compans, Richard W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884748/
https://www.ncbi.nlm.nih.gov/pubmed/33603732
http://dx.doi.org/10.3389/fimmu.2020.583251
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author Vassilieva, Elena V.
Li, Song
Korniychuk, Heorhiy
Taylor, Dahnide M.
Wang, Shelly
Prausnitz, Mark R.
Compans, Richard W.
author_facet Vassilieva, Elena V.
Li, Song
Korniychuk, Heorhiy
Taylor, Dahnide M.
Wang, Shelly
Prausnitz, Mark R.
Compans, Richard W.
author_sort Vassilieva, Elena V.
collection PubMed
description Current strategies for improving protective response to influenza vaccines during immunosenescence do not adequately protect individuals over 65 years of age. Here, we used an aged mouse model to investigate the potential of co-delivery of influenza vaccine with the recently identified combination of a saponin adjuvant Quil-A and an activator of the STING pathway, 2’3 cyclic guanosine monophosphate–adenosine monophosphate (cGAMP) via dissolving microneedle patches (MNPs) applied to skin. We demonstrate that synergy between the two adjuvant components is observed after their incorporation with H1N1 vaccine into MNPs as revealed by analysis of the immune responses in adult mice. Aged 21-month-old mice were found to be completely protected against live influenza challenge after vaccination with the MNPs adjuvanted with the Quil-A/cGAMP combination (5 µg each) and demonstrated significantly reduced morbidity compared to the observed responses in these mice vaccinated with unadjuvanted MNPs. Analysis of the lung lysates of the surviving aged mice post challenge revealed the lowest level of residual inflammation in the adjuvanted groups. We conclude that combining influenza vaccine with a STING pathway activator and saponin-based adjuvant in MNPs is a novel option for skin vaccination of the immunosenescent population, which is at high risk for influenza.
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spelling pubmed-78847482021-02-17 cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model Vassilieva, Elena V. Li, Song Korniychuk, Heorhiy Taylor, Dahnide M. Wang, Shelly Prausnitz, Mark R. Compans, Richard W. Front Immunol Immunology Current strategies for improving protective response to influenza vaccines during immunosenescence do not adequately protect individuals over 65 years of age. Here, we used an aged mouse model to investigate the potential of co-delivery of influenza vaccine with the recently identified combination of a saponin adjuvant Quil-A and an activator of the STING pathway, 2’3 cyclic guanosine monophosphate–adenosine monophosphate (cGAMP) via dissolving microneedle patches (MNPs) applied to skin. We demonstrate that synergy between the two adjuvant components is observed after their incorporation with H1N1 vaccine into MNPs as revealed by analysis of the immune responses in adult mice. Aged 21-month-old mice were found to be completely protected against live influenza challenge after vaccination with the MNPs adjuvanted with the Quil-A/cGAMP combination (5 µg each) and demonstrated significantly reduced morbidity compared to the observed responses in these mice vaccinated with unadjuvanted MNPs. Analysis of the lung lysates of the surviving aged mice post challenge revealed the lowest level of residual inflammation in the adjuvanted groups. We conclude that combining influenza vaccine with a STING pathway activator and saponin-based adjuvant in MNPs is a novel option for skin vaccination of the immunosenescent population, which is at high risk for influenza. Frontiers Media S.A. 2021-02-02 /pmc/articles/PMC7884748/ /pubmed/33603732 http://dx.doi.org/10.3389/fimmu.2020.583251 Text en Copyright © 2021 Vassilieva, Li, Korniychuk, Taylor, Wang, Prausnitz and Compans http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Vassilieva, Elena V.
Li, Song
Korniychuk, Heorhiy
Taylor, Dahnide M.
Wang, Shelly
Prausnitz, Mark R.
Compans, Richard W.
cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title_full cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title_fullStr cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title_full_unstemmed cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title_short cGAMP/Saponin Adjuvant Combination Improves Protective Response to Influenza Vaccination by Microneedle Patch in an Aged Mouse Model
title_sort cgamp/saponin adjuvant combination improves protective response to influenza vaccination by microneedle patch in an aged mouse model
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884748/
https://www.ncbi.nlm.nih.gov/pubmed/33603732
http://dx.doi.org/10.3389/fimmu.2020.583251
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