Timescales of influenza A/H3N2 antibody dynamics.

Human immunity influences the evolution and impact of influenza strains. Because individuals are infected with multiple influenza strains during their lifetime, and each virus can generate a cross-reactive antibody response, it is challenging to quantify the processes that shape observed immune resp...

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Main Authors: Adam J Kucharski, Justin Lessler, Derek A T Cummings, Steven Riley
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-08-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.2004974
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spelling doaj-e329064c1ca94a2eb03ce556436fe3722021-07-02T21:22:17ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852018-08-01168e200497410.1371/journal.pbio.2004974Timescales of influenza A/H3N2 antibody dynamics.Adam J KucharskiJustin LesslerDerek A T CummingsSteven RileyHuman immunity influences the evolution and impact of influenza strains. Because individuals are infected with multiple influenza strains during their lifetime, and each virus can generate a cross-reactive antibody response, it is challenging to quantify the processes that shape observed immune responses or to reliably detect recent infection from serological samples. Using a Bayesian model of antibody dynamics at multiple timescales, we explain complex cross-reactive antibody landscapes by inferring participants' histories of infection with serological data from cross-sectional and longitudinal studies of influenza A/H3N2 in southern China and Vietnam. We find that individual-level influenza antibody profiles can be explained by a short-lived, broadly cross-reactive response that decays within a year to leave a smaller long-term response acting against a narrower range of strains. We also demonstrate that accounting for dynamic immune responses alongside infection history can provide a more accurate alternative to traditional definitions of seroconversion for the estimation of infection attack rates. Our work provides a general model for quantifying aspects of influenza immunity acting at multiple timescales based on contemporary serological data and suggests a two-armed immune response to influenza infection consistent with competitive dynamics between B cell populations. This approach to analysing multiple timescales for antigenic responses could also be applied to other multistrain pathogens such as dengue and related flaviviruses.https://doi.org/10.1371/journal.pbio.2004974
collection DOAJ
language English
format Article
sources DOAJ
author Adam J Kucharski
Justin Lessler
Derek A T Cummings
Steven Riley
spellingShingle Adam J Kucharski
Justin Lessler
Derek A T Cummings
Steven Riley
Timescales of influenza A/H3N2 antibody dynamics.
PLoS Biology
author_facet Adam J Kucharski
Justin Lessler
Derek A T Cummings
Steven Riley
author_sort Adam J Kucharski
title Timescales of influenza A/H3N2 antibody dynamics.
title_short Timescales of influenza A/H3N2 antibody dynamics.
title_full Timescales of influenza A/H3N2 antibody dynamics.
title_fullStr Timescales of influenza A/H3N2 antibody dynamics.
title_full_unstemmed Timescales of influenza A/H3N2 antibody dynamics.
title_sort timescales of influenza a/h3n2 antibody dynamics.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2018-08-01
description Human immunity influences the evolution and impact of influenza strains. Because individuals are infected with multiple influenza strains during their lifetime, and each virus can generate a cross-reactive antibody response, it is challenging to quantify the processes that shape observed immune responses or to reliably detect recent infection from serological samples. Using a Bayesian model of antibody dynamics at multiple timescales, we explain complex cross-reactive antibody landscapes by inferring participants' histories of infection with serological data from cross-sectional and longitudinal studies of influenza A/H3N2 in southern China and Vietnam. We find that individual-level influenza antibody profiles can be explained by a short-lived, broadly cross-reactive response that decays within a year to leave a smaller long-term response acting against a narrower range of strains. We also demonstrate that accounting for dynamic immune responses alongside infection history can provide a more accurate alternative to traditional definitions of seroconversion for the estimation of infection attack rates. Our work provides a general model for quantifying aspects of influenza immunity acting at multiple timescales based on contemporary serological data and suggests a two-armed immune response to influenza infection consistent with competitive dynamics between B cell populations. This approach to analysing multiple timescales for antigenic responses could also be applied to other multistrain pathogens such as dengue and related flaviviruses.
url https://doi.org/10.1371/journal.pbio.2004974
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