<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cevirgel A</submitter><funding>Innovative Medicines Initiative</funding><funding>Dutch Ministry of Health, Welfare and Sport</funding><funding>Ministerie van Volksgezondheid, Welzijn en Sport</funding><pagination>e13703</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9577949</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(10)</volume><pubmed_abstract>Immunosenescence describes immune dysfunction observed in older individuals. To identify individuals at-risk for immune dysfunction, it is crucial to understand the diverse immune phenotypes and their intrinsic functional capabilities. We investigated immune cell subsets and variation in the aging population. We observed that inter-individual immune variation was associated with age and cytomegalovirus seropositivity. Based on the similarities of immune subset composition among individuals, we identified nine immunotypes that displayed different aging-associated immune signatures, which explained inter-individual variation better than age. Additionally, we correlated the immune subset composition of individuals over approximately a year as a measure of stability of immune parameters. Immun</pubmed_abstract><journal>Aging cell</journal><pubmed_title>Identification of aging-associated immunotypes and immune stability as indicators of post-vaccination immune activation.</pubmed_title><pmcid>PMC9577949</pmcid><funding_grant_id>806776</funding_grant_id><pubmed_authors>van Baarle D</pubmed_authors><pubmed_authors>Cevirgel A</pubmed_authors><pubmed_authors>Vos M</pubmed_authors><pubmed_authors>Beckers L</pubmed_authors><pubmed_authors>Buisman AM</pubmed_authors><pubmed_authors>Bijvank E</pubmed_authors><pubmed_authors>Rots N</pubmed_authors><pubmed_authors>Nanlohy NM</pubmed_authors><pubmed_authors>Shetty SA</pubmed_authors><pubmed_authors>van Beek J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of aging-associated immunotypes and immune stability as indicators of post-vaccination immune activation.</name><description>Immunosenescence describes immune dysfunction observed in older individuals. To identify individuals at-risk for immune dysfunction, it is crucial to understand the diverse immune phenotypes and their intrinsic functional capabilities. We investigated immune cell subsets and variation in the aging population. We observed that inter-individual immune variation was associated with age and cytomegalovirus seropositivity. Based on the similarities of immune subset composition among individuals, we identified nine immunotypes that displayed different aging-associated immune signatures, which explained inter-individual variation better than age. Additionally, we correlated the immune subset composition of individuals over approximately a year as a measure of stability of immune parameters. Immun</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T07:13:19.569Z</modification><creation>2025-04-04T07:13:19.569Z</creation></dates><accession>S-EPMC9577949</accession><cross_references><pubmed>36081314</pubmed><doi>10.1111/acel.13703</doi></cross_references></HashMap>