Molecular insights into metabolite antigen recognition by mucosal-associated invariant T cells

被引:8
|
作者
Awad, Wael [1 ,2 ]
Ciacchi, Lisa [1 ,2 ]
McCluskey, James [3 ]
Fairlie, David P. [4 ]
Rossjohn, Jamie [1 ,2 ,5 ]
机构
[1] Monash Univ, Infect & Immun Program, Clayton, Vic 3800, Australia
[2] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[3] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Vic 3000, Australia
[4] Univ Queensland, Inst Mol Biosci, ARC Ctr Excellence Innovat Peptide & Prot Sci, Brisbane, Qld 4072, Australia
[5] Cardiff Univ, Inst Infect & Immun, Sch Med, Heath Pk, Cardiff CF14 4XN, Wales
基金
澳大利亚研究理事会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
RECEPTOR HETEROGENEITY; ACTIVATION; PATHWAY;
D O I
10.1016/j.coi.2023.102351
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Metabolite-based T-cell immunity is emerging as a major player in antimicrobial immunity, autoimmunity, and cancer. Here, small-molecule metabolites were identified to be captured and presented by the major histocompatibility complex class-I-related molecule (MR1) to T cells, namely mucosal-associated invariant T cells (MAIT) and diverse MR1-restricted T cells. Both MR1 and MAIT are evolutionarily conserved in many mammals, suggesting important roles in host immunity. Rational chemical modifications of these naturally occurring metabolites, termed altered metabolite ligands (AMLs), have advanced our understanding of the molecular correlates of MAIT T cell receptor (TCR)-MR1 recognition. This review provides a generalized framework for metabolite recognition and modulation of MAIT cells.
引用
收藏
页数:8
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