<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Walkenhorst M</submitter><funding>Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research)</funding><funding>Deutsche Forschungsgemeinschaft (German Research Foundation)</funding><pagination>9287</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11519641</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Mucosal-associated invariant T (MAIT) cells express semi-invariant T cell receptors (TCR) for recognizing bacterial and yeast antigens derived from riboflavin metabolites presented on the non-polymorphic MHC class I-related protein 1 (MR1). Neuroinflammation in multiple sclerosis (MS) is likely initiated by autoreactive T cells and perpetuated by infiltration of additional immune cells, but the precise role of MAIT cells in MS pathogenesis remains unknown. Here, we use experimental autoimmune encephalomyelitis (EAE), a mouse model of MS, and find an accumulation of MAIT cells in the inflamed central nervous system (CNS) enriched for MAIT17 (RORγt&lt;sup>+&lt;/sup>) and MAIT1/17 (T-bet&lt;sup>+&lt;/sup>RORγt&lt;sup>+&lt;/sup>) subsets with inflammatory and protective features. Results from transcriptome prof</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Protective effect of TCR-mediated MAIT cell activation during experimental autoimmune encephalomyelitis.</pubmed_title><pmcid>PMC11519641</pmcid><funding_grant_id>01GI1605C</funding_grant_id><funding_grant_id>Grant No. 470154978; WI 5322/2-1</funding_grant_id><pubmed_authors>Sonner JK</pubmed_authors><pubmed_authors>Winschel I</pubmed_authors><pubmed_authors>Unger L</pubmed_authors><pubmed_authors>Lantz O</pubmed_authors><pubmed_authors>Woo MS</pubmed_authors><pubmed_authors>Raich L</pubmed_authors><pubmed_authors>Winkler I</pubmed_authors><pubmed_authors>Walkenhorst M</pubmed_authors><pubmed_authors>Meurs N</pubmed_authors><pubmed_authors>Vieira V</pubmed_authors><pubmed_authors>Willing A</pubmed_authors><pubmed_authors>Bauer S</pubmed_authors><pubmed_authors>Salinas G</pubmed_authors><pubmed_authors>Engler JB</pubmed_authors><pubmed_authors>Friese MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protective effect of TCR-mediated MAIT cell activation during experimental autoimmune encephalomyelitis.</name><description>Mucosal-associated invariant T (MAIT) cells express semi-invariant T cell receptors (TCR) for recognizing bacterial and yeast antigens derived from riboflavin metabolites presented on the non-polymorphic MHC class I-related protein 1 (MR1). Neuroinflammation in multiple sclerosis (MS) is likely initiated by autoreactive T cells and perpetuated by infiltration of additional immune cells, but the precise role of MAIT cells in MS pathogenesis remains unknown. Here, we use experimental autoimmune encephalomyelitis (EAE), a mouse model of MS, and find an accumulation of MAIT cells in the inflamed central nervous system (CNS) enriched for MAIT17 (RORγt&lt;sup>+&lt;/sup>) and MAIT1/17 (T-bet&lt;sup>+&lt;/sup>RORγt&lt;sup>+&lt;/sup>) subsets with inflammatory and protective features. Results from transcriptome prof</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-05T09:12:14.989Z</modification><creation>2025-04-05T09:12:14.989Z</creation></dates><accession>S-EPMC11519641</accession><cross_references><pubmed>39468055</pubmed><doi>10.1038/s41467-024-53657-9</doi></cross_references></HashMap>