<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Antoni AC</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pubmed_abstract>Sepsis is associated with profound immune dysregulation that increases the risk for life-threatening secondary infections: Dendritic cells (DCs) undergo functional reprogramming due to yet unknown changes during differentiation in the bone marrow (BM). In parallel, lymphopenia and exhaustion of T lymphocytes interfere with antigen-specific adaptive immunity. We hypothesized that there exists a link between T cells and the modulation of DC differentiation in the BM during murine polymicrobial sepsis. Sepsis was induced by cecal ligation and puncture (CLP), a model for human bacterial sepsis. At different time points after CLP, the BM and spleen were analyzed in terms of T-cell subpopulations, activation, and Interferon (IFN)-γ synthesis as well as the number of pre-DCs. BM-derived DCs were </pubmed_abstract><journal>Frontiers in immunology</journal><pagination>945409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9488929</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TLR2-induced CD8&lt;sup>+&lt;/sup> T-cell deactivation shapes dendritic cell differentiation in the bone marrow during sepsis.</pubmed_title><pmcid>PMC9488929</pmcid><pubmed_authors>Klein-Hitpaß L</pubmed_authors><pubmed_authors>Antoni AC</pubmed_authors><pubmed_authors>Jablonska J</pubmed_authors><pubmed_authors>Dudda M</pubmed_authors><pubmed_authors>Budeus B</pubmed_authors><pubmed_authors>Pylaeva E</pubmed_authors><pubmed_authors>Flohe SB</pubmed_authors></additional><is_claimable>false</is_claimable><name>TLR2-induced CD8&lt;sup>+&lt;/sup> T-cell deactivation shapes dendritic cell differentiation in the bone marrow during sepsis.</name><description>Sepsis is associated with profound immune dysregulation that increases the risk for life-threatening secondary infections: Dendritic cells (DCs) undergo functional reprogramming due to yet unknown changes during differentiation in the bone marrow (BM). In parallel, lymphopenia and exhaustion of T lymphocytes interfere with antigen-specific adaptive immunity. We hypothesized that there exists a link between T cells and the modulation of DC differentiation in the BM during murine polymicrobial sepsis. Sepsis was induced by cecal ligation and puncture (CLP), a model for human bacterial sepsis. At different time points after CLP, the BM and spleen were analyzed in terms of T-cell subpopulations, activation, and Interferon (IFN)-γ synthesis as well as the number of pre-DCs. BM-derived DCs were </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-28T04:23:25.534Z</modification><creation>2025-04-07T02:17:36.829Z</creation></dates><accession>S-EPMC9488929</accession><cross_references><pubmed>36148245</pubmed><doi>10.3389/fimmu.2022.945409</doi></cross_references></HashMap>