<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Durand A</submitter><pubmed_abstract>Despite being implicated in non-lymphoid tissues, non-recirculating T cells may also exist in secondary lymphoid organs (SLO). However, a detailed characterization of this lymphoid-resident T cell pool has not yet been done. Here we show that a substantial proportion of CD4 regulatory (Treg) and memory (Tmem) cells establish long-term residence in the SLOs of specific pathogen-free mice. Of these SLOs, only T cell residence within Peyer's patches is affected by microbiota. Resident CD4 Treg and CD4 Tmem cells from lymph nodes and non-lymphoid tissues share many phenotypic and functional characteristics. The percentage of resident T cells in SLOs increases considerably with age, with S1PR1 downregulation possibly contributing to this altered homeostasis. Our results thus show that T cell re</pubmed_abstract><journal>Nature communications</journal><pagination>68</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5754350</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Profiling the lymphoid-resident T cell pool reveals modulation by age and microbiota.</pubmed_title><pmcid>PMC5754350</pmcid><pubmed_authors>Bonilla N</pubmed_authors><pubmed_authors>Guichard V</pubmed_authors><pubmed_authors>Mattiuz R</pubmed_authors><pubmed_authors>Durand A</pubmed_authors><pubmed_authors>Audemard-Verger A</pubmed_authors><pubmed_authors>Riviere M</pubmed_authors><pubmed_authors>Martin B</pubmed_authors><pubmed_authors>Lucas B</pubmed_authors><pubmed_authors>Delon J</pubmed_authors><pubmed_authors>Delpoux A</pubmed_authors><pubmed_authors>Hamon P</pubmed_authors><pubmed_authors>Boissonnas A</pubmed_authors><pubmed_authors>Auffray C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Profiling the lymphoid-resident T cell pool reveals modulation by age and microbiota.</name><description>Despite being implicated in non-lymphoid tissues, non-recirculating T cells may also exist in secondary lymphoid organs (SLO). However, a detailed characterization of this lymphoid-resident T cell pool has not yet been done. Here we show that a substantial proportion of CD4 regulatory (Treg) and memory (Tmem) cells establish long-term residence in the SLOs of specific pathogen-free mice. Of these SLOs, only T cell residence within Peyer's patches is affected by microbiota. Resident CD4 Treg and CD4 Tmem cells from lymph nodes and non-lymphoid tissues share many phenotypic and functional characteristics. The percentage of resident T cells in SLOs increases considerably with age, with S1PR1 downregulation possibly contributing to this altered homeostasis. Our results thus show that T cell re</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2026-05-02T17:42:34.243Z</modification><creation>2025-06-01T12:02:45.513Z</creation></dates><accession>S-EPMC5754350</accession><cross_references><pubmed>29302034</pubmed><doi>10.1038/s41467-017-02458-4</doi></cross_references></HashMap>