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Life course exposures continually shape antibody profiles and risk of seroconversion to influenza
Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across indi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377380/ https://www.ncbi.nlm.nih.gov/pubmed/32702069 http://dx.doi.org/10.1371/journal.ppat.1008635 |
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author | Yang, Bingyi Lessler, Justin Zhu, Huachen Jiang, Chao Qiang Read, Jonathan M. Hay, James A. Kwok, Kin On Shen, Ruiyin Guan, Yi Riley, Steven Cummings, Derek A. T. |
author_facet | Yang, Bingyi Lessler, Justin Zhu, Huachen Jiang, Chao Qiang Read, Jonathan M. Hay, James A. Kwok, Kin On Shen, Ruiyin Guan, Yi Riley, Steven Cummings, Derek A. T. |
author_sort | Yang, Bingyi |
collection | PubMed |
description | Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across individuals and determine future responses is unclear. We used hemagglutination inhibition titers from 21 H3N2 strains to construct 777 paired antibody profiles from people aged 2 to 86, and developed novel metrics to capture features of these profiles. Total antibody titer per potential influenza exposure increases in early life, then decreases in middle age. Increased titers to one or more strains were seen in 97.8% of participants during a roughly four-year interval, suggesting widespread influenza exposure. While titer changes were seen to all strains, recently circulating strains exhibited the greatest titer rise. Higher pre-existing, homologous titers at baseline reduced the risk of seroconversion to recent strains. After adjusting for homologous titer, we also found an increased frequency of seroconversion against recent strains among those with higher immunity to older previously exposed strains. Including immunity to previously exposures also improved the deviance explained by the models. Our results suggest that a comprehensive quantitative description of immunity encompassing past exposures could lead to improved correlates of risk of influenza infection. |
format | Online Article Text |
id | pubmed-7377380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73773802020-08-12 Life course exposures continually shape antibody profiles and risk of seroconversion to influenza Yang, Bingyi Lessler, Justin Zhu, Huachen Jiang, Chao Qiang Read, Jonathan M. Hay, James A. Kwok, Kin On Shen, Ruiyin Guan, Yi Riley, Steven Cummings, Derek A. T. PLoS Pathog Research Article Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across individuals and determine future responses is unclear. We used hemagglutination inhibition titers from 21 H3N2 strains to construct 777 paired antibody profiles from people aged 2 to 86, and developed novel metrics to capture features of these profiles. Total antibody titer per potential influenza exposure increases in early life, then decreases in middle age. Increased titers to one or more strains were seen in 97.8% of participants during a roughly four-year interval, suggesting widespread influenza exposure. While titer changes were seen to all strains, recently circulating strains exhibited the greatest titer rise. Higher pre-existing, homologous titers at baseline reduced the risk of seroconversion to recent strains. After adjusting for homologous titer, we also found an increased frequency of seroconversion against recent strains among those with higher immunity to older previously exposed strains. Including immunity to previously exposures also improved the deviance explained by the models. Our results suggest that a comprehensive quantitative description of immunity encompassing past exposures could lead to improved correlates of risk of influenza infection. Public Library of Science 2020-07-23 /pmc/articles/PMC7377380/ /pubmed/32702069 http://dx.doi.org/10.1371/journal.ppat.1008635 Text en © 2020 Yang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yang, Bingyi Lessler, Justin Zhu, Huachen Jiang, Chao Qiang Read, Jonathan M. Hay, James A. Kwok, Kin On Shen, Ruiyin Guan, Yi Riley, Steven Cummings, Derek A. T. Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title | Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title_full | Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title_fullStr | Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title_full_unstemmed | Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title_short | Life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
title_sort | life course exposures continually shape antibody profiles and risk of seroconversion to influenza |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377380/ https://www.ncbi.nlm.nih.gov/pubmed/32702069 http://dx.doi.org/10.1371/journal.ppat.1008635 |
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