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Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children
Different vaccine strains included in the live attenuated influenza vaccine (LAIV) have variable efficacy. The reasons for this are not clear and may include differences in immunogenicity. We report a Phase IV open‐label study on the immunogenicity of a single dose of quadrivalent LAIV (Fluenz™ Tetr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954673/ https://www.ncbi.nlm.nih.gov/pubmed/31670841 http://dx.doi.org/10.1111/cei.13395 |
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author | Turner, P. J. Abdulla, A. F. Cole, M. E. Javan, R. R. Gould, V. O'Driscoll, M. E. Southern, J. Zambon, M. Miller, E. Andrews, N. J. Höschler, K. Tregoning, J. S. |
author_facet | Turner, P. J. Abdulla, A. F. Cole, M. E. Javan, R. R. Gould, V. O'Driscoll, M. E. Southern, J. Zambon, M. Miller, E. Andrews, N. J. Höschler, K. Tregoning, J. S. |
author_sort | Turner, P. J. |
collection | PubMed |
description | Different vaccine strains included in the live attenuated influenza vaccine (LAIV) have variable efficacy. The reasons for this are not clear and may include differences in immunogenicity. We report a Phase IV open‐label study on the immunogenicity of a single dose of quadrivalent LAIV (Fluenz™ Tetra) in children during the 2015/16 season, to investigate the antibody responses to different strains. Eligible children were enrolled to receive LAIV; nasal samples were collected before and approximately 4 weeks after immunization. There was a significant increase in nasal immunoglobulin (Ig)A to the H3N2, B/Victoria lineage (B/Brisbane) and B/Yamagata lineage (B/Phuket) components, but not to the H1N1 component. The fold change in nasal IgA response was inversely proportional to the baseline nasal IgA titre for H1N1, H3N2 and B/Brisbane. We investigated possible associations that may explain baseline nasal IgA, including age and prior vaccination status, but found different patterns for different antigens, suggesting that the response is multi‐factorial. Overall, we observed differences in immune responses to different viral strains included in the vaccine; the reasons for this require further investigation. |
format | Online Article Text |
id | pubmed-6954673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69546732020-01-17 Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children Turner, P. J. Abdulla, A. F. Cole, M. E. Javan, R. R. Gould, V. O'Driscoll, M. E. Southern, J. Zambon, M. Miller, E. Andrews, N. J. Höschler, K. Tregoning, J. S. Clin Exp Immunol Editors' Choice Different vaccine strains included in the live attenuated influenza vaccine (LAIV) have variable efficacy. The reasons for this are not clear and may include differences in immunogenicity. We report a Phase IV open‐label study on the immunogenicity of a single dose of quadrivalent LAIV (Fluenz™ Tetra) in children during the 2015/16 season, to investigate the antibody responses to different strains. Eligible children were enrolled to receive LAIV; nasal samples were collected before and approximately 4 weeks after immunization. There was a significant increase in nasal immunoglobulin (Ig)A to the H3N2, B/Victoria lineage (B/Brisbane) and B/Yamagata lineage (B/Phuket) components, but not to the H1N1 component. The fold change in nasal IgA response was inversely proportional to the baseline nasal IgA titre for H1N1, H3N2 and B/Brisbane. We investigated possible associations that may explain baseline nasal IgA, including age and prior vaccination status, but found different patterns for different antigens, suggesting that the response is multi‐factorial. Overall, we observed differences in immune responses to different viral strains included in the vaccine; the reasons for this require further investigation. John Wiley and Sons Inc. 2019-11-15 2020-02 /pmc/articles/PMC6954673/ /pubmed/31670841 http://dx.doi.org/10.1111/cei.13395 Text en © 2019 The Authors. Clinical & Experimental Immunology published by John Wiley & Sons Ltd on behalf of British Society for Immunology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Editors' Choice Turner, P. J. Abdulla, A. F. Cole, M. E. Javan, R. R. Gould, V. O'Driscoll, M. E. Southern, J. Zambon, M. Miller, E. Andrews, N. J. Höschler, K. Tregoning, J. S. Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title | Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title_full | Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title_fullStr | Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title_full_unstemmed | Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title_short | Differences in nasal immunoglobulin A responses to influenza vaccine strains after live attenuated influenza vaccine (LAIV) immunization in children |
title_sort | differences in nasal immunoglobulin a responses to influenza vaccine strains after live attenuated influenza vaccine (laiv) immunization in children |
topic | Editors' Choice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954673/ https://www.ncbi.nlm.nih.gov/pubmed/31670841 http://dx.doi.org/10.1111/cei.13395 |
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