Please use this identifier to cite or link to this item: https://doi.org/10.7554/eLife.24476
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dc.titleFunctionally diverse human T cells recognize non-microbial antigens presented by MR1
dc.contributor.authorLepore, M
dc.contributor.authorKalinichenko, A
dc.contributor.authorCalogero, S
dc.contributor.authorKumar, P
dc.contributor.authorPaleja, B
dc.contributor.authorSchmaler, M
dc.contributor.authorNarang, V
dc.contributor.authorZolezzi, F
dc.contributor.authorPoidinger, M
dc.contributor.authorMori, L
dc.contributor.authorde Libero, G
dc.date.accessioned2020-10-21T07:52:23Z
dc.date.available2020-10-21T07:52:23Z
dc.date.issued2017
dc.identifier.citationLepore, M, Kalinichenko, A, Calogero, S, Kumar, P, Paleja, B, Schmaler, M, Narang, V, Zolezzi, F, Poidinger, M, Mori, L, de Libero, G (2017). Functionally diverse human T cells recognize non-microbial antigens presented by MR1. eLife 6 : e24476. ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.24476
dc.identifier.issn2050084X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178676
dc.description.abstractMHC class I-related molecule MR1 presents riboflavin-and folate-related metabolites to mucosal-associated invariant T cells, but it is unknown whether MR1 can present alternative antigens to other T cell lineages. In healthy individuals we identified MR1-restricted T cells (named MR1T cells) displaying diverse TCRs and reacting to MR1-expressing cells in the absence of microbial ligands. Analysis of MR1T cell clones revealed specificity for distinct cell-derived antigens and alternative transcriptional strategies for metabolic programming, cell cycle control and functional polarization following antigen stimulation. Phenotypic and functional characterization of MR1T cell clones showed multiple chemokine receptor expression profiles and secretion of diverse effector molecules, suggesting functional heterogeneity. Accordingly, MR1T cells exhibited distinct T helper-like capacities upon MR1-dependent recognition of target cells expressing physiological levels of surface MR1. These data extend the role of MR1 beyond microbial antigen presentation and indicate MR1T cells are a normal part of the human T cell repertoire. © Lepore et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectCD137 antigen
dc.subjectCD69 antigen
dc.subjectCD83 antigen
dc.subjectCD86 antigen
dc.subjectchemokine receptor CCR4
dc.subjectchemokine receptor CCR6
dc.subjectchemokine receptor CXCR3
dc.subjectearly growth response factor 1
dc.subjectgamma interferon
dc.subjectinterferon regulatory factor 4
dc.subjectinterleukin 10
dc.subjectinterleukin 2
dc.subjectinterleukin 3
dc.subjectinterleukin 4
dc.subjectinterleukin 5
dc.subjectinterleukin 6
dc.subjectlymphotoxin
dc.subjectmajor histocompatibility antigen class 1
dc.subjectmajor histocompatibility complex class 1 related gene protein
dc.subjectmucin 2
dc.subjectprotein c fos
dc.subjectretinoid X receptor alpha
dc.subjectT lymphocyte receptor alpha chain
dc.subjectT lymphocyte receptor beta chain
dc.subjecttranscription factor FOXP3
dc.subjecttranscription factor JunB
dc.subjecttranscription factor T bet
dc.subjecttranscriptome
dc.subjecttumor necrosis factor
dc.subjectunclassified drug
dc.subjectunindexed drug
dc.subjectantigen
dc.subjectchemokine receptor
dc.subjectcytokine
dc.subjectHLA antigen class 1
dc.subjectminor histocompatibility antigen
dc.subjectMR1 protein, human
dc.subjectanimal cell
dc.subjectantigen recognition
dc.subjectArticle
dc.subjectcell fractionation
dc.subjectcontrolled study
dc.subjectcytokine release
dc.subjectdown regulation
dc.subjectenzyme linked immunosorbent assay
dc.subjectflow cytometry
dc.subjectfluorescence activated cell sorting
dc.subjectgene expression
dc.subjectgene transfer
dc.subjecthuman
dc.subjecthuman cell
dc.subjectimmunostimulation
dc.subjectnext generation sequencing
dc.subjectnonhuman
dc.subjectnucleotide sequence
dc.subjectprotein expression
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA sequence
dc.subjectT lymphocyte
dc.subjectT lymphocyte activation
dc.subjectupregulation
dc.subjectWestern blotting
dc.subjectantigen presentation
dc.subjectbiosynthesis
dc.subjectcell line
dc.subjectimmunology
dc.subjectmetabolism
dc.subjectsecretion (process)
dc.subjectT lymphocyte
dc.subjectAntigen Presentation
dc.subjectAntigens
dc.subjectCell Line
dc.subjectCytokines
dc.subjectHistocompatibility Antigens Class I
dc.subjectHumans
dc.subjectMinor Histocompatibility Antigens
dc.subjectReceptors, Chemokine
dc.subjectT-Lymphocytes
dc.typeArticle
dc.contributor.departmentBIOLOGY (NU)
dc.description.doi10.7554/eLife.24476
dc.description.sourcetitleeLife
dc.description.volume6
dc.description.pagee24476
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