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Promiscuous recognition of MR1 drives self-reactive mucosal-associated invariant T cell responses.

Andrew ChancellorRobert Alan SimmonsRahul C KhanolkarVladimir NosiAisha BeshirovaGiuliano BerloffaRodrigo ColomboVijaykumar KaruppiahJohanne M PentierVanessa M TubbHemza GhadbaneRichard J SucklingKeith PageRory M CreanAlessandro VacchiniCorinne De GregorioVerena SchaeferDaniel ConstantinThomas GligorisAngharad LloydMiriam HockVelupillai SrikannathasanRoss A RobinsonGurdyal S BesraMarc W Van der KampLucia MoriRaffaele Adolfo CalogeroDavid K ColeGennaro De LiberoMarco Lepore
Published in: The Journal of experimental medicine (2023)
Mucosal-associated invariant T (MAIT) cells use canonical semi-invariant T cell receptors (TCR) to recognize microbial riboflavin precursors displayed by the antigen-presenting molecule MR1. The extent of MAIT TCR crossreactivity toward physiological, microbially unrelated antigens remains underexplored. We describe MAIT TCRs endowed with MR1-dependent reactivity to tumor and healthy cells in the absence of microbial metabolites. MAIT cells bearing TCRs crossreactive toward self are rare but commonly found within healthy donors and display T-helper-like functions in vitro. Experiments with MR1-tetramers loaded with distinct ligands revealed significant crossreactivity among MAIT TCRs both ex vivo and upon in vitro expansion. A canonical MAIT TCR was selected on the basis of extremely promiscuous MR1 recognition. Structural and molecular dynamic analyses associated promiscuity to unique TCRβ-chain features that were enriched within self-reactive MAIT cells of healthy individuals. Thus, self-reactive recognition of MR1 represents a functionally relevant indication of MAIT TCR crossreactivity, suggesting a potentially broader role of MAIT cells in immune homeostasis and diseases, beyond microbial immunosurveillance.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • regulatory t cells
  • magnetic resonance
  • contrast enhanced
  • oxidative stress
  • drug delivery
  • cell death
  • dendritic cells
  • computed tomography
  • single cell
  • cancer therapy