MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage

J Exp Med. 2014 Jul 28;211(8):1601-10. doi: 10.1084/jem.20140507. Epub 2014 Jul 21.

Abstract

Mucosal-associated invariant T (MAIT) cells express a semi-invariant T cell receptor (TCR) that detects microbial metabolites presented by the nonpolymorphic major histocompatibility complex (MHC)-like molecule MR1. The highly conserved nature of MR1 in conjunction with biased MAIT TCRα chain usage is widely thought to indicate limited ligand presentation and discrimination within a pattern-like recognition system. Here, we evaluated the TCR repertoire of MAIT cells responsive to three classes of microbes. Substantial diversity and heterogeneity were apparent across the functional MAIT cell repertoire as a whole, especially for TCRβ chain sequences. Moreover, different pathogen-specific responses were characterized by distinct TCR usage, both between and within individuals, suggesting that MAIT cell adaptation was a direct consequence of exposure to various exogenous MR1-restricted epitopes. In line with this interpretation, MAIT cell clones with distinct TCRs responded differentially to a riboflavin metabolite. These results suggest that MAIT cells can discriminate between pathogen-derived ligands in a clonotype-dependent manner, providing a basis for adaptive memory via recruitment of specific repertoires shaped by microbial exposure.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antigens, Differentiation, B-Lymphocyte / metabolism*
  • Bacteria / drug effects
  • Bacteria / immunology*
  • Cell Line
  • Clone Cells
  • Complementarity Determining Regions / chemistry
  • Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor / genetics
  • Histocompatibility Antigens Class I / metabolism*
  • Histocompatibility Antigens Class II / metabolism*
  • Humans
  • Ligands
  • Minor Histocompatibility Antigens
  • Molecular Sequence Data
  • Mucous Membrane / cytology*
  • Mucous Membrane / drug effects
  • Mucous Membrane / immunology*
  • Receptors, Antigen, T-Cell / metabolism*
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Sequence Homology, Amino Acid
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism*
  • Vitamin B Complex / pharmacology

Substances

  • Antigens, Differentiation, B-Lymphocyte
  • Complementarity Determining Regions
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Ligands
  • MR1 protein, human
  • Minor Histocompatibility Antigens
  • Receptors, Antigen, T-Cell
  • Receptors, Antigen, T-Cell, alpha-beta
  • invariant chain
  • Vitamin B Complex