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Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses

Pre-existing immunity to influenza is dependent on a number of factors and can vary greatly within and across influenza subtypes. In this study, volunteers (aged 18–85 years) were vaccinated with split, inactivated Fluzone(TM) in four consecutive influenza seasons from 2013 to 2016. The impact of re...

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Autores principales: Carlock, Michael A., Ingram, John G., Clutter, Emily F., Cecil, Noah C., Ramgopal, Moti, Zimmerman, Richard K., Warren, William, Kleanthous, Harry, Ross, Ted M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773397/
https://www.ncbi.nlm.nih.gov/pubmed/31291153
http://dx.doi.org/10.1080/21645515.2019.1642056
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author Carlock, Michael A.
Ingram, John G.
Clutter, Emily F.
Cecil, Noah C.
Ramgopal, Moti
Zimmerman, Richard K.
Warren, William
Kleanthous, Harry
Ross, Ted M.
author_facet Carlock, Michael A.
Ingram, John G.
Clutter, Emily F.
Cecil, Noah C.
Ramgopal, Moti
Zimmerman, Richard K.
Warren, William
Kleanthous, Harry
Ross, Ted M.
author_sort Carlock, Michael A.
collection PubMed
description Pre-existing immunity to influenza is dependent on a number of factors and can vary greatly within and across influenza subtypes. In this study, volunteers (aged 18–85 years) were vaccinated with split, inactivated Fluzone(TM) in four consecutive influenza seasons from 2013 to 2016. The impact of repeat vaccination on breadth and durability of functional antibodies was assessed for total IgG and IgA anti-hemagglutinin (HA) binding antibodies and hemagglutination-inhibition (HAI) activity against both influenza B lineages. Many subjects were able to maintain high seroprotective titers to the vaccine strains in subsequent years, which resulted in low vaccine-induced seroconversion rates. This was especially evident in younger subjects who typically had higher titers and maintained these titers into the following season. In contrast, the HAI titers in elderly subjects were generally lower and more likely to decline prior to the start of the next influenza season. Immunological recall or ‘back-boosting’ to antigenically related viruses was associated with seroconversion. Overall, influenza vaccination in both younger and older people elicited broadly reactive immune responses within a lineage, as well as cross-reactive immune responses between lineages. This study exemplified the impact that age and influenza exposure history have on determining an individual’s ability to respond to future influenza infections.
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spelling pubmed-67733972019-10-11 Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses Carlock, Michael A. Ingram, John G. Clutter, Emily F. Cecil, Noah C. Ramgopal, Moti Zimmerman, Richard K. Warren, William Kleanthous, Harry Ross, Ted M. Hum Vaccin Immunother Research Paper Pre-existing immunity to influenza is dependent on a number of factors and can vary greatly within and across influenza subtypes. In this study, volunteers (aged 18–85 years) were vaccinated with split, inactivated Fluzone(TM) in four consecutive influenza seasons from 2013 to 2016. The impact of repeat vaccination on breadth and durability of functional antibodies was assessed for total IgG and IgA anti-hemagglutinin (HA) binding antibodies and hemagglutination-inhibition (HAI) activity against both influenza B lineages. Many subjects were able to maintain high seroprotective titers to the vaccine strains in subsequent years, which resulted in low vaccine-induced seroconversion rates. This was especially evident in younger subjects who typically had higher titers and maintained these titers into the following season. In contrast, the HAI titers in elderly subjects were generally lower and more likely to decline prior to the start of the next influenza season. Immunological recall or ‘back-boosting’ to antigenically related viruses was associated with seroconversion. Overall, influenza vaccination in both younger and older people elicited broadly reactive immune responses within a lineage, as well as cross-reactive immune responses between lineages. This study exemplified the impact that age and influenza exposure history have on determining an individual’s ability to respond to future influenza infections. Taylor & Francis 2019-08-08 /pmc/articles/PMC6773397/ /pubmed/31291153 http://dx.doi.org/10.1080/21645515.2019.1642056 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Carlock, Michael A.
Ingram, John G.
Clutter, Emily F.
Cecil, Noah C.
Ramgopal, Moti
Zimmerman, Richard K.
Warren, William
Kleanthous, Harry
Ross, Ted M.
Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title_full Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title_fullStr Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title_full_unstemmed Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title_short Impact of age and pre-existing immunity on the induction of human antibody responses against influenza B viruses
title_sort impact of age and pre-existing immunity on the induction of human antibody responses against influenza b viruses
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773397/
https://www.ncbi.nlm.nih.gov/pubmed/31291153
http://dx.doi.org/10.1080/21645515.2019.1642056
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