MAITs, MR1 and vitamin B metabolites

被引:63
作者
Birkinshaw, Richard W. [1 ]
Kjer-Nielsen, Lars [2 ]
Eckle, Sidonia B. G. [2 ]
McCluskey, James [2 ]
Rossjohn, Jamie [1 ,3 ]
机构
[1] Monash Univ, Sch Biomed Sci, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[2] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[3] Cardiff Univ, Sch Med, Inst Infect & Immun, Cardiff CF14 4XN, S Glam, Wales
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
INVARIANT T-CELLS; BACTERIAL-INFECTION; RECOGNITION; RECEPTOR; ANTIGENS; GLYCOLIPIDS; REPERTOIRE; SELECTION; CD1B; TCR;
D O I
10.1016/j.coi.2013.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
alpha beta T-cell mediated immunity is traditionally characterised by recognition of peptides or lipids presented by the major histocompatibility complex (MHC) or the CD1 family respectively. Recently the antigenic repertoire of alpha beta T-cells has been expanded with the observation that mucosal-associated invariant T-cells (MAIT cells), an abundant population of innate-like T-cells, can recognise metabolites of vitamin B, when presented by the MHC-related protein, MR1. The semi-invariant MAIT T-cell antigen receptor (TCR) recognises riboflavin and folic acid metabolites bound by MR1 in a conserved docking mode, and thus acts like a pattern recognition receptor. Here we review and discuss the recent observations concerning antigen presentation by MR1, the advent of MR1-Ag tetramers that specifically stain MAIT cells, recognition by the MAIT TCR, and our emerging understanding of MAIT cells in disease.
引用
收藏
页码:7 / 13
页数:7
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