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

Andrew Chancellor, Robert Alan Simmons, Rahul C Khanolkar,Vladimir Nosi, Aisha Beshirova, Giuliano Berloffa, Rodrigo Colombo,Vijaykumar Karuppiah,Johanne M Pentier, Vanessa Tubb,Hemza Ghadbane, Richard J Suckling, Keith Page,Rory M Crean,Alessandro Vacchini,Corinne De Gregorio, Verena Schaefer, Daniel Constantin, Thomas Gligoris,Angharad Lloyd,Miriam Hock,Velupillai Srikannathasan,Ross A Robinson,Gurdyal S Besra,Marc W van der Kamp,Lucia Mori,Raffaele Calogero,David K Cole,Gennaro De Libero,Marco Lepore

The Journal of experimental medicine(2023)

引用 2|浏览12
暂无评分
摘要
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.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要