<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tomas-Ojer P</submitter><funding>European Research Council</funding><pagination>790884</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8852676</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>Antigen-induced T-cell exhaustion and T-cell senescence are peripheral regulatory mechanisms that control effector T-cell responses. Markers of exhaustion and senescence on T Cells indicate the previous activation by repetitive stimulation with specific antigens. Malignant tumors are accompanied by enhanced T-cell exhaustion and T-cell senescence resulting in immune evasion, while these control mechanisms might be diminished in autoimmune diseases including multiple sclerosis (MS). To better understand the involvement of antigen-induced T-cell senescence in controlling CD4+ T-cell-mediated autoimmune responses in MS, we have analyzed the re-expression of CD45RA and the downregulation of CD28 and CD27 molecules as markers of antigen-induced T-cell senescence in fresh cerebrospinal fluid (CS</pubmed_abstract><journal>Frontiers in neurology</journal><pubmed_title>Characterization of Antigen-Induced CD4+ T-Cell Senescence in Multiple Sclerosis.</pubmed_title><pmcid>PMC8852676</pmcid><funding_grant_id>340733</funding_grant_id><pubmed_authors>Docampo MJ</pubmed_authors><pubmed_authors>Cruciani C</pubmed_authors><pubmed_authors>Sospedra M</pubmed_authors><pubmed_authors>Puthenparampil M</pubmed_authors><pubmed_authors>Tomas-Ojer P</pubmed_authors><pubmed_authors>Martin R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of Antigen-Induced CD4+ T-Cell Senescence in Multiple Sclerosis.</name><description>Antigen-induced T-cell exhaustion and T-cell senescence are peripheral regulatory mechanisms that control effector T-cell responses. Markers of exhaustion and senescence on T Cells indicate the previous activation by repetitive stimulation with specific antigens. Malignant tumors are accompanied by enhanced T-cell exhaustion and T-cell senescence resulting in immune evasion, while these control mechanisms might be diminished in autoimmune diseases including multiple sclerosis (MS). To better understand the involvement of antigen-induced T-cell senescence in controlling CD4+ T-cell-mediated autoimmune responses in MS, we have analyzed the re-expression of CD45RA and the downregulation of CD28 and CD27 molecules as markers of antigen-induced T-cell senescence in fresh cerebrospinal fluid (CS</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T20:50:23.652Z</modification><creation>2025-04-04T20:50:23.652Z</creation></dates><accession>S-EPMC8852676</accession><cross_references><pubmed>35185762</pubmed><doi>10.3389/fneur.2022.790884</doi></cross_references></HashMap>