<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Bents SJ</submitter><funding>NIAID NIH HHS</funding><funding>Wellcome Trust</funding><pubmed_abstract>The rebound of endemic respiratory viruses following the COVID-19 pandemic was marked by atypical transmission dynamics, with children experiencing increased disease burden and out-of-season epidemics as restrictions relaxed. Here we used serology from a newly developed quantitative multiplex assay to assess the post-pandemic immunity debt, a drop in immunity due to a lack of endemic virus circulation during COVID-19. We assessed age-specific antibody dynamics in Seattle, Washington, US, across a broad range of respiratory viruses, including influenza, respiratory syncytial virus, seasonal coronaviruses, and SARS-CoV-2. We found that respiratory virus immunodynamics differed between individuals &lt;5 years of age and older individuals, with young children experiencing both larger boosts and q</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2025.03.26.25324738</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12478342</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multiplex serology reveals age-specific immunodynamics of endemic respiratory pathogens in the wake of the COVID-19 pandemic.</pubmed_title><pmcid>PMC12478342</pmcid><funding_grant_id>75N93021C00015</funding_grant_id><funding_grant_id>225001/Z/22/Z</funding_grant_id><pubmed_authors>Hansen C</pubmed_authors><pubmed_authors>Blazevic R</pubmed_authors><pubmed_authors>Han P</pubmed_authors><pubmed_authors>Bents SJ</pubmed_authors><pubmed_authors>Steven-Ayers T</pubmed_authors><pubmed_authors>Waghmare A</pubmed_authors><pubmed_authors>Andrews C</pubmed_authors><pubmed_authors>Kimball L</pubmed_authors><pubmed_authors>Englund JA</pubmed_authors><pubmed_authors>Boeckh M</pubmed_authors><pubmed_authors>Starita L</pubmed_authors><pubmed_authors>Adler A</pubmed_authors><pubmed_authors>Perofsky A</pubmed_authors><pubmed_authors>Wolter N</pubmed_authors><pubmed_authors>Prentice R</pubmed_authors><pubmed_authors>Moyes J</pubmed_authors><pubmed_authors>Martin ET</pubmed_authors><pubmed_authors>Krantz EM</pubmed_authors><pubmed_authors>Viboud C</pubmed_authors><pubmed_authors>von Gottberg A</pubmed_authors><pubmed_authors>Cohen C</pubmed_authors><pubmed_authors>Hay JA</pubmed_authors><pubmed_authors>Maake L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiplex serology reveals age-specific immunodynamics of endemic respiratory pathogens in the wake of the COVID-19 pandemic.</name><description>The rebound of endemic respiratory viruses following the COVID-19 pandemic was marked by atypical transmission dynamics, with children experiencing increased disease burden and out-of-season epidemics as restrictions relaxed. Here we used serology from a newly developed quantitative multiplex assay to assess the post-pandemic immunity debt, a drop in immunity due to a lack of endemic virus circulation during COVID-19. We assessed age-specific antibody dynamics in Seattle, Washington, US, across a broad range of respiratory viruses, including influenza, respiratory syncytial virus, seasonal coronaviruses, and SARS-CoV-2. We found that respiratory virus immunodynamics differed between individuals &lt;5 years of age and older individuals, with young children experiencing both larger boosts and q</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-01T03:09:23.537Z</modification><creation>2026-07-01T03:07:36.586Z</creation></dates><accession>S-EPMC12478342</accession><cross_references><pubmed>41030929</pubmed><doi>10.1101/2025.03.26.25324738</doi></cross_references></HashMap>