Birth cohort relative to an influenza A virus's antigenic cluster introduction drives patterns of children's antibody titers
An individual's antibody titers to influenza A strains are a result of the complicated interplay between infection history, cross-reactivity, immune waning, and other factors. It has been challenging to disentangle how population-level patterns of humoral immunity change as a function of age, c...
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description | An individual's antibody titers to influenza A strains are a result of the complicated interplay between infection history, cross-reactivity, immune waning, and other factors. It has been challenging to disentangle how population-level patterns of humoral immunity change as a function of age, calendar year, and birth cohort from cross-sectional data alone. We analyzed 1,589 longitudinal sera samples from 260 children across three studies in Nicaragua, 2006-16. Hemagglutination inhibition (HAI) titers were determined against four H3N2 strains, one H1N1 strain, and two H1N1pdm strains. We assessed temporal patterns of HAI titers using an age-period-cohort modeling framework. We found that titers against a given virus depended on calendar year of serum collection and birth cohort but not on age. Titer cohort patterns were better described by participants' ages relative to year of likely introduction of the virus's antigenic cluster than by age relative to year of strain introduction or by year of birth. These cohort effects may be driven by a decreasing likelihood of early-life infection after cluster introduction and by more broadly reactive antibodies at a young age. H3N2 and H1N1 viruses had qualitatively distinct cohort patterns, with cohort patterns of titers to specific H3N2 strains reaching their peak in children born 3 years prior to that virus's antigenic cluster introduction and with titers to H1N1 and H1N1pdm strains peaking for children born 1-2 years prior to cluster introduction but not being dramatically lower for older children. Ultimately, specific patterns of strain circulation and antigenic cluster introduction may drive population-level antibody titer patterns in children. |
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It has been challenging to disentangle how population-level patterns of humoral immunity change as a function of age, calendar year, and birth cohort from cross-sectional data alone. We analyzed 1,589 longitudinal sera samples from 260 children across three studies in Nicaragua, 2006-16. Hemagglutination inhibition (HAI) titers were determined against four H3N2 strains, one H1N1 strain, and two H1N1pdm strains. We assessed temporal patterns of HAI titers using an age-period-cohort modeling framework. We found that titers against a given virus depended on calendar year of serum collection and birth cohort but not on age. Titer cohort patterns were better described by participants' ages relative to year of likely introduction of the virus's antigenic cluster than by age relative to year of strain introduction or by year of birth. These cohort effects may be driven by a decreasing likelihood of early-life infection after cluster introduction and by more broadly reactive antibodies at a young age. H3N2 and H1N1 viruses had qualitatively distinct cohort patterns, with cohort patterns of titers to specific H3N2 strains reaching their peak in children born 3 years prior to that virus's antigenic cluster introduction and with titers to H1N1 and H1N1pdm strains peaking for children born 1-2 years prior to cluster introduction but not being dramatically lower for older children. Ultimately, specific patterns of strain circulation and antigenic cluster introduction may drive population-level antibody titer patterns in children.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1010317</identifier><identifier>PMID: 35192673</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Age ; Antibodies ; Antibodies, Viral ; Antigenic determinants ; Antigens ; Biology and Life Sciences ; Birth Cohort ; Calendars ; Child ; Children ; Clusters ; Cohort analysis ; Cross-reactivity ; Cross-Sectional Studies ; Demographic aspects ; Evaluation ; Health aspects ; Hemagglutination inhibition ; Hemagglutination Inhibition Tests ; Humans ; Humoral immunity ; Immune response ; Immunology ; Infections ; Influenza ; Influenza A ; Influenza A Virus, H1N1 Subtype ; Influenza A Virus, H3N2 Subtype ; Influenza Vaccines ; Influenza viruses ; Influenza, Human - epidemiology ; Laboratories ; Medicine and Health Sciences ; Pandemics ; Pediatrics ; People and Places ; Physiological aspects ; Population ; Research and Analysis Methods ; Strains (organisms) ; Swine flu ; Vaccines ; Viral antibodies ; Viruses</subject><ispartof>PLoS pathogens, 2022-02, Vol.18 (2), p.e1010317-e1010317</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>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 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). 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These cohort effects may be driven by a decreasing likelihood of early-life infection after cluster introduction and by more broadly reactive antibodies at a young age. H3N2 and H1N1 viruses had qualitatively distinct cohort patterns, with cohort patterns of titers to specific H3N2 strains reaching their peak in children born 3 years prior to that virus's antigenic cluster introduction and with titers to H1N1 and H1N1pdm strains peaking for children born 1-2 years prior to cluster introduction but not being dramatically lower for older children. Ultimately, specific patterns of strain circulation and antigenic cluster introduction may drive population-level antibody titer patterns in children.</description><subject>Adolescent</subject><subject>Age</subject><subject>Antibodies</subject><subject>Antibodies, Viral</subject><subject>Antigenic determinants</subject><subject>Antigens</subject><subject>Biology and Life Sciences</subject><subject>Birth Cohort</subject><subject>Calendars</subject><subject>Child</subject><subject>Children</subject><subject>Clusters</subject><subject>Cohort analysis</subject><subject>Cross-reactivity</subject><subject>Cross-Sectional Studies</subject><subject>Demographic aspects</subject><subject>Evaluation</subject><subject>Health aspects</subject><subject>Hemagglutination inhibition</subject><subject>Hemagglutination Inhibition Tests</subject><subject>Humans</subject><subject>Humoral immunity</subject><subject>Immune response</subject><subject>Immunology</subject><subject>Infections</subject><subject>Influenza</subject><subject>Influenza A</subject><subject>Influenza A Virus, H1N1 Subtype</subject><subject>Influenza A Virus, H3N2 Subtype</subject><subject>Influenza Vaccines</subject><subject>Influenza viruses</subject><subject>Influenza, Human - 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It has been challenging to disentangle how population-level patterns of humoral immunity change as a function of age, calendar year, and birth cohort from cross-sectional data alone. We analyzed 1,589 longitudinal sera samples from 260 children across three studies in Nicaragua, 2006-16. Hemagglutination inhibition (HAI) titers were determined against four H3N2 strains, one H1N1 strain, and two H1N1pdm strains. We assessed temporal patterns of HAI titers using an age-period-cohort modeling framework. We found that titers against a given virus depended on calendar year of serum collection and birth cohort but not on age. Titer cohort patterns were better described by participants' ages relative to year of likely introduction of the virus's antigenic cluster than by age relative to year of strain introduction or by year of birth. These cohort effects may be driven by a decreasing likelihood of early-life infection after cluster introduction and by more broadly reactive antibodies at a young age. H3N2 and H1N1 viruses had qualitatively distinct cohort patterns, with cohort patterns of titers to specific H3N2 strains reaching their peak in children born 3 years prior to that virus's antigenic cluster introduction and with titers to H1N1 and H1N1pdm strains peaking for children born 1-2 years prior to cluster introduction but not being dramatically lower for older children. 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subjects | Adolescent Age Antibodies Antibodies, Viral Antigenic determinants Antigens Biology and Life Sciences Birth Cohort Calendars Child Children Clusters Cohort analysis Cross-reactivity Cross-Sectional Studies Demographic aspects Evaluation Health aspects Hemagglutination inhibition Hemagglutination Inhibition Tests Humans Humoral immunity Immune response Immunology Infections Influenza Influenza A Influenza A Virus, H1N1 Subtype Influenza A Virus, H3N2 Subtype Influenza Vaccines Influenza viruses Influenza, Human - epidemiology Laboratories Medicine and Health Sciences Pandemics Pediatrics People and Places Physiological aspects Population Research and Analysis Methods Strains (organisms) Swine flu Vaccines Viral antibodies Viruses |
title | Birth cohort relative to an influenza A virus's antigenic cluster introduction drives patterns of children's antibody titers |
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