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

Authors :
Chancellor A
Alan Simmons R
Khanolkar RC
Nosi V
Beshirova A
Berloffa G
Colombo R
Karuppiah V
Pentier JM
Tubb V
Ghadbane H
Suckling RJ
Page K
Crean RM
Vacchini A
De Gregorio C
Schaefer V
Constantin D
Gligoris T
Lloyd A
Hock M
Srikannathasan V
Robinson RA
Besra GS
van der Kamp MW
Mori L
Calogero R
Cole DK
De Libero G
Lepore M
Source :
The Journal of experimental medicine [J Exp Med] 2023 Sep 04; Vol. 220 (9). Date of Electronic Publication: 2023 Jun 29.
Publication Year :
2023

Abstract

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.<br /> (© 2023 Chancellor et al.)

Details

Language :
English
ISSN :
1540-9538
Volume :
220
Issue :
9
Database :
MEDLINE
Journal :
The Journal of experimental medicine
Publication Type :
Academic Journal
Accession number :
37382893
Full Text :
https://doi.org/10.1084/jem.20221939