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

نویسندگان

  • Marco Lepore
  • Artem Kalinichenko
  • Salvatore Calogero
  • Pavanish Kumar
  • Bhairav Paleja
  • Mathias Schmaler
  • Vipin Narang
  • Francesca Zolezzi
  • Michael Poidinger
  • Lucia Mori
  • Gennaro De Libero
چکیده

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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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2017