4.8 Article

Functionally diverse human T cells recognize non-microbial antigens presented by MR1

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ELIFE
卷 6, 期 -, 页码 -

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ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.24476

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  1. Schweizerischer Nationalfonds zur Forderung der Wissenschaftlichen Forschung [310030-149571]
  2. European Commission [643381]
  3. Science and Engineering Research Council [1121480006]
  4. Universitat Basel [Core Funding]
  5. Agency for Science, Technology and Research [1201826277, SIgN, Core Funds]
  6. DBM, University Hospital Basel [Core Funds]
  7. Horizon Framework Programme [TBVAC 2020 643381]
  8. Swiss National Science Foundation (SNF) [310030_149571] Funding Source: Swiss National Science Foundation (SNF)

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MHC 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.

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