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PD-1-expressing MAIT cells from patients with tuberculosis exhibit elevated production of CXCL13.

Authors :
Jiang J
Cao Z
Qu J
Liu H
Han H
Cheng X
Source :
Scandinavian journal of immunology [Scand J Immunol] 2020 Apr; Vol. 91 (4), pp. e12858. Date of Electronic Publication: 2020 Jan 08.
Publication Year :
2020

Abstract

To understand functional role of PD-1-expressing MAIT cells during tuberculosis infection in humans, sorted PD-1 <superscript>+</superscript> and PD-1 <superscript>-</superscript> MAIT cells from pleural effusions of patients with pleural tuberculosis were subjected to transcriptome sequencing. PD-1-expressing MAIT cells were analysed by flow cytometry and their phenotypic and functional features were investigated. Transcriptome sequencing identified 144 genes that were differentially expressed between PD-1 <superscript>+</superscript> and PD-1 <superscript>-</superscript> MAIT cells from tuberculous pleural effusions and CXCL13 was the gene with highest fold difference. The level of PD-1-expressing MAIT cells was associated with extent of TB infection in humans. PD-1-expressing MAIT cells had increased production of CXCL13 and IL-21 as determined by flow cytometry. PD-1 <superscript>high</superscript> CXCR5 <superscript>-</superscript> MAIT cells were significantly expanded in pleural effusions from patients with pleural tuberculosis as compared with those from peripheral blood of both patients with tuberculosis and healthy controls. Although PD-1 <superscript>high</superscript> CXCR5 <superscript>-</superscript> MAIT cells from tuberculous pleural effusions had reduced IFN-γ level and increased expression of Tim-3 and GITR, they showed activated phenotype and had higher glucose uptake and lipid content. It is concluded that PD-1-expressing MAIT cells had reduced IFN-γ level but increased production of both CXCL13 and IL-21.<br /> (© 2019 The Scandinavian Foundation for Immunology.)

Details

Language :
English
ISSN :
1365-3083
Volume :
91
Issue :
4
Database :
MEDLINE
Journal :
Scandinavian journal of immunology
Publication Type :
Academic Journal
Accession number :
31833092
Full Text :
https://doi.org/10.1111/sji.12858