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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2018-08-01
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Online Access: | https://doi.org/10.1371/journal.pbio.2004974 |
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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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