<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Conway J</submitter><funding>British Heart Foundation</funding><funding>Academy of Medical Sciences Springboard Award</funding><funding>MRC-Versus Arthritis Centre for Musculoskeletal Ageing Research. GA is supported by an MRC Programme Grant</funding><pagination>e14401</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11896561</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(3)</volume><pubmed_abstract>The intestinal epithelium serves as a physical and functional barrier against harmful substances, preventing their entry into the circulation and subsequent induction of a systemic immune response. Gut barrier dysfunction has recently emerged as a feature of ageing linked to declining health, and increased intestinal membrane permeability has been shown to promote heightened systemic inflammation in aged hosts. Concurrent with age-related changes in the gut microbiome, the thymic microenvironment undergoes a series of morphological, phenotypical and architectural alterations with age, including disorganisation of the corticomedullary junction, increased fibrosis, increased thymic adiposity and the accumulation of senescent cells. However, a direct link between gut barrier dysbiosis and thy</pubmed_abstract><journal>Aging cell</journal><pubmed_title>Age-related loss of intestinal barrier integrity plays an integral role in thymic involution and T cell ageing.</pubmed_title><pmcid>PMC11896561</pmcid><funding_grant_id>SBF0051132</funding_grant_id><funding_grant_id>MR/T029765/1</funding_grant_id><pubmed_authors>Dugan B</pubmed_authors><pubmed_authors>Conway J</pubmed_authors><pubmed_authors>Bowdish DME</pubmed_authors><pubmed_authors>Sharma-Oates A</pubmed_authors><pubmed_authors>Sullivan J</pubmed_authors><pubmed_authors>White AJ</pubmed_authors><pubmed_authors>Mauro C</pubmed_authors><pubmed_authors>van Schaik W</pubmed_authors><pubmed_authors>Lamberte LE</pubmed_authors><pubmed_authors>Parnell SM</pubmed_authors><pubmed_authors>Duggal NA</pubmed_authors><pubmed_authors>De Jong EN</pubmed_authors><pubmed_authors>Anderson G</pubmed_authors><pubmed_authors>Rees NP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Age-related loss of intestinal barrier integrity plays an integral role in thymic involution and T cell ageing.</name><description>The intestinal epithelium serves as a physical and functional barrier against harmful substances, preventing their entry into the circulation and subsequent induction of a systemic immune response. Gut barrier dysfunction has recently emerged as a feature of ageing linked to declining health, and increased intestinal membrane permeability has been shown to promote heightened systemic inflammation in aged hosts. Concurrent with age-related changes in the gut microbiome, the thymic microenvironment undergoes a series of morphological, phenotypical and architectural alterations with age, including disorganisation of the corticomedullary junction, increased fibrosis, increased thymic adiposity and the accumulation of senescent cells. However, a direct link between gut barrier dysbiosis and thy</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-26T02:45:28.274Z</modification><creation>2025-04-06T10:34:01.797Z</creation></dates><accession>S-EPMC11896561</accession><cross_references><pubmed>39547946</pubmed><doi>10.1111/acel.14401</doi></cross_references></HashMap>