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Age-specific differences in the dynamics of protective immunity to influenza
Influenza A viruses evolve rapidly to escape host immunity, causing reinfection. The form and duration of protection after each influenza virus infection are poorly understood. We quantify the dynamics of protective immunity by fitting individual-level mechanistic models to longitudinal serology fro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458119/ https://www.ncbi.nlm.nih.gov/pubmed/30971703 http://dx.doi.org/10.1038/s41467-019-09652-6 |
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author | Ranjeva, Sylvia Subramanian, Rahul Fang, Vicky J. Leung, Gabriel M. Ip, Dennis K. M. Perera, Ranawaka A. P. M. Peiris, J. S. Malik Cowling, Benjamin J. Cobey, Sarah |
author_facet | Ranjeva, Sylvia Subramanian, Rahul Fang, Vicky J. Leung, Gabriel M. Ip, Dennis K. M. Perera, Ranawaka A. P. M. Peiris, J. S. Malik Cowling, Benjamin J. Cobey, Sarah |
author_sort | Ranjeva, Sylvia |
collection | PubMed |
description | Influenza A viruses evolve rapidly to escape host immunity, causing reinfection. The form and duration of protection after each influenza virus infection are poorly understood. We quantify the dynamics of protective immunity by fitting individual-level mechanistic models to longitudinal serology from children and adults. We find that most protection in children but not adults correlates with antibody titers to the hemagglutinin surface protein. Protection against circulating strains wanes to half of peak levels 3.5–7 years after infection in both age groups, and wanes faster against influenza A(H3N2) than A(H1N1)pdm09. Protection against H3N2 lasts longer in adults than in children. Our results suggest that influenza antibody responses shift focus with age from the mutable hemagglutinin head to other epitopes, consistent with the theory of original antigenic sin, and might affect protection. Imprinting, or primary infection with a subtype, has modest to no effect on the risk of non-medically attended infections in adults. |
format | Online Article Text |
id | pubmed-6458119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64581192019-04-12 Age-specific differences in the dynamics of protective immunity to influenza Ranjeva, Sylvia Subramanian, Rahul Fang, Vicky J. Leung, Gabriel M. Ip, Dennis K. M. Perera, Ranawaka A. P. M. Peiris, J. S. Malik Cowling, Benjamin J. Cobey, Sarah Nat Commun Article Influenza A viruses evolve rapidly to escape host immunity, causing reinfection. The form and duration of protection after each influenza virus infection are poorly understood. We quantify the dynamics of protective immunity by fitting individual-level mechanistic models to longitudinal serology from children and adults. We find that most protection in children but not adults correlates with antibody titers to the hemagglutinin surface protein. Protection against circulating strains wanes to half of peak levels 3.5–7 years after infection in both age groups, and wanes faster against influenza A(H3N2) than A(H1N1)pdm09. Protection against H3N2 lasts longer in adults than in children. Our results suggest that influenza antibody responses shift focus with age from the mutable hemagglutinin head to other epitopes, consistent with the theory of original antigenic sin, and might affect protection. Imprinting, or primary infection with a subtype, has modest to no effect on the risk of non-medically attended infections in adults. Nature Publishing Group UK 2019-04-10 /pmc/articles/PMC6458119/ /pubmed/30971703 http://dx.doi.org/10.1038/s41467-019-09652-6 Text en © The Author(s) 2019 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 Ranjeva, Sylvia Subramanian, Rahul Fang, Vicky J. Leung, Gabriel M. Ip, Dennis K. M. Perera, Ranawaka A. P. M. Peiris, J. S. Malik Cowling, Benjamin J. Cobey, Sarah Age-specific differences in the dynamics of protective immunity to influenza |
title | Age-specific differences in the dynamics of protective immunity to influenza |
title_full | Age-specific differences in the dynamics of protective immunity to influenza |
title_fullStr | Age-specific differences in the dynamics of protective immunity to influenza |
title_full_unstemmed | Age-specific differences in the dynamics of protective immunity to influenza |
title_short | Age-specific differences in the dynamics of protective immunity to influenza |
title_sort | age-specific differences in the dynamics of protective immunity to influenza |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458119/ https://www.ncbi.nlm.nih.gov/pubmed/30971703 http://dx.doi.org/10.1038/s41467-019-09652-6 |
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