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Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains

Seasonal influenza vaccine formulas change almost every year yet information about how this affects the antibody repertoire of vaccine recipients is inadequate. New vaccine virus strains are selected, replacing older strains to better match the currently circulating strains. But even while the vacci...

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Autores principales: Plant, Ewan P., Fredell, Lucy J., Hatcher, Blake A., Li, Xing, Chiang, Meng-Jung, Kosikova, Martina, Xie, Hang, Zoueva, Olga, Cost, Angelia A., Ye, Zhiping, Cooper, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507920/
https://www.ncbi.nlm.nih.gov/pubmed/28701762
http://dx.doi.org/10.1038/s41598-017-05579-4
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author Plant, Ewan P.
Fredell, Lucy J.
Hatcher, Blake A.
Li, Xing
Chiang, Meng-Jung
Kosikova, Martina
Xie, Hang
Zoueva, Olga
Cost, Angelia A.
Ye, Zhiping
Cooper, Michael J.
author_facet Plant, Ewan P.
Fredell, Lucy J.
Hatcher, Blake A.
Li, Xing
Chiang, Meng-Jung
Kosikova, Martina
Xie, Hang
Zoueva, Olga
Cost, Angelia A.
Ye, Zhiping
Cooper, Michael J.
author_sort Plant, Ewan P.
collection PubMed
description Seasonal influenza vaccine formulas change almost every year yet information about how this affects the antibody repertoire of vaccine recipients is inadequate. New vaccine virus strains are selected, replacing older strains to better match the currently circulating strains. But even while the vaccine is being manufactured the circulating strains can evolve. The ideal response to a seasonal vaccine would maintain antibodies toward existing strains that might continue to circulate, and to generate cross-reactive antibodies, particularly towards conserved influenza epitopes, potentially limiting infections caused by newly evolving strains. Here we use the hemagglutination inhibition assay to analyze the antibody repertoire in subjects vaccinated two years in a row with either identical vaccine virus strains or with differing vaccine virus strains. The data indicates that changing the vaccine formulation results in an antibody repertoire that is better able to react with strains emerging after the vaccine virus strains are selected. The effect is observed for both influenza A and B strains in groups of subjects vaccinated in three different seasons. Analyses include stratification by age and sex.
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spelling pubmed-55079202017-07-14 Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains Plant, Ewan P. Fredell, Lucy J. Hatcher, Blake A. Li, Xing Chiang, Meng-Jung Kosikova, Martina Xie, Hang Zoueva, Olga Cost, Angelia A. Ye, Zhiping Cooper, Michael J. Sci Rep Article Seasonal influenza vaccine formulas change almost every year yet information about how this affects the antibody repertoire of vaccine recipients is inadequate. New vaccine virus strains are selected, replacing older strains to better match the currently circulating strains. But even while the vaccine is being manufactured the circulating strains can evolve. The ideal response to a seasonal vaccine would maintain antibodies toward existing strains that might continue to circulate, and to generate cross-reactive antibodies, particularly towards conserved influenza epitopes, potentially limiting infections caused by newly evolving strains. Here we use the hemagglutination inhibition assay to analyze the antibody repertoire in subjects vaccinated two years in a row with either identical vaccine virus strains or with differing vaccine virus strains. The data indicates that changing the vaccine formulation results in an antibody repertoire that is better able to react with strains emerging after the vaccine virus strains are selected. The effect is observed for both influenza A and B strains in groups of subjects vaccinated in three different seasons. Analyses include stratification by age and sex. Nature Publishing Group UK 2017-07-12 /pmc/articles/PMC5507920/ /pubmed/28701762 http://dx.doi.org/10.1038/s41598-017-05579-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Plant, Ewan P.
Fredell, Lucy J.
Hatcher, Blake A.
Li, Xing
Chiang, Meng-Jung
Kosikova, Martina
Xie, Hang
Zoueva, Olga
Cost, Angelia A.
Ye, Zhiping
Cooper, Michael J.
Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title_full Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title_fullStr Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title_full_unstemmed Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title_short Different Repeat Annual Influenza Vaccinations Improve the Antibody Response to Drifted Influenza Strains
title_sort different repeat annual influenza vaccinations improve the antibody response to drifted influenza strains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507920/
https://www.ncbi.nlm.nih.gov/pubmed/28701762
http://dx.doi.org/10.1038/s41598-017-05579-4
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