<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramirez SI</submitter><funding>NIAID NIH HHS</funding><pagination>630-636</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11895801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>632(8025)</volume><pubmed_abstract>The upper airway is an important site of infection, but immune memory in the human upper airway is poorly understood, with implications for COVID-19 and many other human diseases&lt;sup>1-4&lt;/sup>. Here we demonstrate that nasal and nasopharyngeal swabs can be used to obtain insights into these challenging problems, and define distinct immune cell populations, including antigen-specific memory B cells and T cells, in two adjacent anatomical sites in the upper airway. Upper airway immune cell populations seemed stable over time in healthy adults undergoing monthly swabs for more than 1 year, and prominent tissue resident memory T (T&lt;sub>RM&lt;/sub>) cell and B (B&lt;sub>RM&lt;/sub>) cell populations were defined. Unexpectedly, germinal centre cells were identified consistently in many nasopharyngeal swa</pubmed_abstract><journal>Nature</journal><pubmed_title>Immunological memory diversity in the human upper airway.</pubmed_title><pmcid>PMC11895801</pmcid><funding_grant_id>T32 AI007036</funding_grant_id><funding_grant_id>U19 AI142742</funding_grant_id><pubmed_authors>Levi G</pubmed_authors><pubmed_authors>Lopez PG</pubmed_authors><pubmed_authors>Kim HJ</pubmed_authors><pubmed_authors>Ramirez SI</pubmed_authors><pubmed_authors>Hastie KM</pubmed_authors><pubmed_authors>Sutton HJ</pubmed_authors><pubmed_authors>Mashoof S</pubmed_authors><pubmed_authors>Stacey HD</pubmed_authors><pubmed_authors>Faraji F</pubmed_authors><pubmed_authors>Hills LB</pubmed_authors><pubmed_authors>Goodwin B</pubmed_authors><pubmed_authors>Crotty S</pubmed_authors><pubmed_authors>Yan CH</pubmed_authors><pubmed_authors>DeConde AS</pubmed_authors><pubmed_authors>Saphire EO</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunological memory diversity in the human upper airway.</name><description>The upper airway is an important site of infection, but immune memory in the human upper airway is poorly understood, with implications for COVID-19 and many other human diseases&lt;sup>1-4&lt;/sup>. Here we demonstrate that nasal and nasopharyngeal swabs can be used to obtain insights into these challenging problems, and define distinct immune cell populations, including antigen-specific memory B cells and T cells, in two adjacent anatomical sites in the upper airway. Upper airway immune cell populations seemed stable over time in healthy adults undergoing monthly swabs for more than 1 year, and prominent tissue resident memory T (T&lt;sub>RM&lt;/sub>) cell and B (B&lt;sub>RM&lt;/sub>) cell populations were defined. Unexpectedly, germinal centre cells were identified consistently in many nasopharyngeal swa</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-04-24T03:21:30.509Z</modification><creation>2025-04-06T22:16:28.938Z</creation></dates><accession>S-EPMC11895801</accession><cross_references><pubmed>39085605</pubmed><doi>10.1038/s41586-024-07748-8</doi></cross_references></HashMap>