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Mucosal Immunol. 2018 Nov;11(6):1591-1605. doi: 10.1038/s41385-018-0072-x. Epub 2018 Aug 16.

Tuning of human MAIT cell activation by commensal bacteria species and MR1-dependent T-cell presentation.

Author information

1
Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
2
Department of Microbiology, NYU School of Medicine, New York, NY, 10016, USA.
3
Department of Chemistry, University of Connecticut, Storrs, CT, 06269, USA.
4
Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA. Derya@mac.com.

Abstract

Human mucosal-associated invariant T (MAIT) cell receptors (TCRs) recognize bacterial riboflavin pathway metabolites through the MHC class 1-related molecule MR1. However, it is unclear whether MAIT cells discriminate between many species of the human microbiota. To address this, we developed an in vitro functional assay through human T cells engineered for MAIT-TCRs (eMAIT-TCRs) stimulated by MR1-expressing antigen-presenting cells (APCs). We then screened 47 microbiota-associated bacterial species from different phyla for their eMAIT-TCR stimulatory capacities. Only bacterial species that encoded the riboflavin pathway were stimulatory for MAIT-TCRs. Most species that were high stimulators belonged to Bacteroidetes and Proteobacteria phyla, whereas low/non-stimulator species were primarily Actinobacteria or Firmicutes. Activation of MAIT cells by high- vs low-stimulating bacteria also correlated with the level of riboflavin they secreted or after bacterial infection of macrophages. Remarkably, we found that human T-cell subsets can also present riboflavin metabolites to MAIT cells in a MR1-restricted fashion. This T-T cell-mediated signaling also induced IFNγ, TNF and granzyme B from MAIT cells, albeit at lower level than professional APC. These findings suggest that MAIT cells can discriminate and categorize complex human microbiota through computation of TCR signals depending on antigen load and presenting cells, and fine-tune their functional responses.

PMID:
30115998
PMCID:
PMC6279574
DOI:
10.1038/s41385-018-0072-x
[Indexed for MEDLINE]
Free PMC Article

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