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Early prediction of antigenic transitions for influenza A/H3N2

Influenza A/H3N2 is a rapidly evolving virus which experiences major antigenic transitions every two to eight years. Anticipating the timing and outcome of transitions is critical to developing effective seasonal influenza vaccines. Using a published phylodynamic model of influenza transmission, we...

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Detalles Bibliográficos
Autores principales: Castro, Lauren A., Bedford, Trevor, Ancel Meyers, Lauren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048310/
https://www.ncbi.nlm.nih.gov/pubmed/32069282
http://dx.doi.org/10.1371/journal.pcbi.1007683
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author Castro, Lauren A.
Bedford, Trevor
Ancel Meyers, Lauren
author_facet Castro, Lauren A.
Bedford, Trevor
Ancel Meyers, Lauren
author_sort Castro, Lauren A.
collection PubMed
description Influenza A/H3N2 is a rapidly evolving virus which experiences major antigenic transitions every two to eight years. Anticipating the timing and outcome of transitions is critical to developing effective seasonal influenza vaccines. Using a published phylodynamic model of influenza transmission, we identified indicators of future evolutionary success for an emerging antigenic cluster and quantified fundamental trade-offs in our ability to make such predictions. The eventual fate of a new cluster depends on its initial epidemiological growth rate––which is a function of mutational load and population susceptibility to the cluster––along with the variance in growth rate across co-circulating viruses. Logistic regression can predict whether a cluster at 5% relative frequency will eventually succeed with ~80% sensitivity, providing up to eight months advance warning. As a cluster expands, the predictions improve while the lead-time for vaccine development and other interventions decreases. However, attempts to make comparable predictions from 12 years of empirical influenza surveillance data, which are far sparser and more coarse-grained, achieve only 56% sensitivity. By expanding influenza surveillance to obtain more granular estimates of the frequencies of and population-wide susceptibility to emerging viruses, we can better anticipate major antigenic transitions. This provides added incentives for accelerating the vaccine production cycle to reduce the lead time required for strain selection.
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spelling pubmed-70483102020-03-09 Early prediction of antigenic transitions for influenza A/H3N2 Castro, Lauren A. Bedford, Trevor Ancel Meyers, Lauren PLoS Comput Biol Research Article Influenza A/H3N2 is a rapidly evolving virus which experiences major antigenic transitions every two to eight years. Anticipating the timing and outcome of transitions is critical to developing effective seasonal influenza vaccines. Using a published phylodynamic model of influenza transmission, we identified indicators of future evolutionary success for an emerging antigenic cluster and quantified fundamental trade-offs in our ability to make such predictions. The eventual fate of a new cluster depends on its initial epidemiological growth rate––which is a function of mutational load and population susceptibility to the cluster––along with the variance in growth rate across co-circulating viruses. Logistic regression can predict whether a cluster at 5% relative frequency will eventually succeed with ~80% sensitivity, providing up to eight months advance warning. As a cluster expands, the predictions improve while the lead-time for vaccine development and other interventions decreases. However, attempts to make comparable predictions from 12 years of empirical influenza surveillance data, which are far sparser and more coarse-grained, achieve only 56% sensitivity. By expanding influenza surveillance to obtain more granular estimates of the frequencies of and population-wide susceptibility to emerging viruses, we can better anticipate major antigenic transitions. This provides added incentives for accelerating the vaccine production cycle to reduce the lead time required for strain selection. Public Library of Science 2020-02-18 /pmc/articles/PMC7048310/ /pubmed/32069282 http://dx.doi.org/10.1371/journal.pcbi.1007683 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Castro, Lauren A.
Bedford, Trevor
Ancel Meyers, Lauren
Early prediction of antigenic transitions for influenza A/H3N2
title Early prediction of antigenic transitions for influenza A/H3N2
title_full Early prediction of antigenic transitions for influenza A/H3N2
title_fullStr Early prediction of antigenic transitions for influenza A/H3N2
title_full_unstemmed Early prediction of antigenic transitions for influenza A/H3N2
title_short Early prediction of antigenic transitions for influenza A/H3N2
title_sort early prediction of antigenic transitions for influenza a/h3n2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048310/
https://www.ncbi.nlm.nih.gov/pubmed/32069282
http://dx.doi.org/10.1371/journal.pcbi.1007683
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