<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Pangrazzi L</submitter><pubmed_abstract>Naïve CD8&lt;sup>+&lt;/sup> T cells are key players of adaptive immunity, but their heterogeneity and age-related changes are not fully understood. This study aimed to compare naïve CD8&lt;sup>+&lt;/sup> T cell subsets defined by different combinations of markers, namely, N&lt;sub>CCR7&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CCR7&lt;sup>+&lt;/sup>), N&lt;sub>CD28&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CD28&lt;sup>+&lt;/sup>), N&lt;sub>CD27&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>), and phenotypically most "true-naïve"-like, N&lt;sub>TN&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CCR7&lt;sup>+&lt;/sup>CD28&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>CD57&lt;sup>-&lt;/sup>). Peripheral blood was harvested from donors of various ages and the phenotype of the four subsets of naïve CD8&lt;sup>+&lt;/sup> T cells was analyzed. N&lt;sub>CD27&lt;/sub> and N&lt;sub>TN&lt;/sub> cells showed similar phenotypes with low expressio</pubmed_abstract><journal>Frontiers in aging</journal><pagination>1765665</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12907349</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phenotypic and functional heterogeneity of naive CD8&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; T cells in human peripheral blood during aging.</pubmed_title><pmcid>PMC12907349</pmcid><pubmed_authors>Chelini G</pubmed_authors><pubmed_authors>Bachmann M</pubmed_authors><pubmed_authors>Pangrazzi L</pubmed_authors><pubmed_authors>Hoffmann L</pubmed_authors><pubmed_authors>Jenewein B</pubmed_authors><pubmed_authors>Weinberger B</pubmed_authors><pubmed_authors>Pehl P</pubmed_authors><pubmed_authors>Keller M</pubmed_authors><pubmed_authors>Cavinato M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phenotypic and functional heterogeneity of naive CD8&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; T cells in human peripheral blood during aging.</name><description>Naïve CD8&lt;sup>+&lt;/sup> T cells are key players of adaptive immunity, but their heterogeneity and age-related changes are not fully understood. This study aimed to compare naïve CD8&lt;sup>+&lt;/sup> T cell subsets defined by different combinations of markers, namely, N&lt;sub>CCR7&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CCR7&lt;sup>+&lt;/sup>), N&lt;sub>CD28&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CD28&lt;sup>+&lt;/sup>), N&lt;sub>CD27&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>), and phenotypically most "true-naïve"-like, N&lt;sub>TN&lt;/sub> (CD45RA&lt;sup>+&lt;/sup>CCR7&lt;sup>+&lt;/sup>CD28&lt;sup>+&lt;/sup>CD27&lt;sup>+&lt;/sup>CD57&lt;sup>-&lt;/sup>). Peripheral blood was harvested from donors of various ages and the phenotype of the four subsets of naïve CD8&lt;sup>+&lt;/sup> T cells was analyzed. N&lt;sub>CD27&lt;/sub> and N&lt;sub>TN&lt;/sub> cells showed similar phenotypes with low expressio</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026</publication><modification>2026-07-10T03:11:51.422Z</modification><creation>2026-07-10T03:08:43.715Z</creation></dates><accession>S-EPMC12907349</accession><cross_references><pubmed>41704679</pubmed><doi>10.3389/fragi.2026.1765665</doi></cross_references></HashMap>