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Journal article

Stimulatory MAIT cell antigens reach the circulation and are efficiently metabolised and presented by human liver cells

Abstract:
Objective
Mucosal-associated invariant T (MAIT) cells are the most abundant T cells in human liver. They respond to bacterial metabolites presented by major histocompatibility complex-like molecule MR1. MAIT cells exert regulatory and antimicrobial functions and are implicated in liver fibrogenesis. It is not well understood which liver cells function as antigen (Ag)-presenting cells for MAIT cells, and under which conditions stimulatory Ags reach the circulation.
Design
We used different types of primary human liver cells in Ag-presentation assays to blood-derived and liver-derived MAIT cells. We assessed MAIT cell stimulatory potential of serum from healthy subjects and patients with portal hypertension undergoing transjugular intrahepatic portosystemic shunt stent, and patients with inflammatory bowel disease (IBD).
Results
MAIT cells were dispersed throughout healthy human liver and all tested liver cell types stimulated MAIT cells, hepatocytes being most efficient. MAIT cell activation by liver cells occurred in response to bacterial lysate and pure Ag, and was prevented by non-activating MR1 ligands. Serum derived from peripheral and portal blood, and from patients with IBD stimulated MAIT cells in MR1-dependent manner.
Conclusion
Our findings reveal previously unrecognised roles of liver cells in Ag metabolism and activation of MAIT cells, repression of which creates an opportunity to design antifibrotic therapies. The presence of MAIT cell stimulatory Ags in serum rationalises the observed activated MAIT cell phenotype in liver. Increased serum levels of gut-derived MAIT cell stimulatory ligands in patients with impaired intestinal barrier function indicate that intrahepatic Ag-presentation may represent an important step in the development of liver disease.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1136/gutjnl-2021-324478

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
ORCID:
0000-0002-7230-9264
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
More by this author
Role:
Author
ORCID:
0000-0003-3390-1633
More by this author
Role:
Author
ORCID:
0000-0002-8362-784X
More by this author
Role:
Author
ORCID:
0000-0003-0690-1232


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Funder identifier:
https://ror.org/029chgv08
Grant:
109965MA
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Funder identifier:
https://ror.org/00yjd3n13
Grant:
PZ00P3_189490
PZ00P3_167828
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Funder identifier:
https://ror.org/02f3xk561


Publisher:
BMJ Publishing Group
Journal:
Gut More from this journal
Volume:
71
Issue:
12
Pages:
2526-2538
Publication date:
2022-01-20
Acceptance date:
2022-01-08
DOI:
EISSN:
1468-3288
ISSN:
0017-5749


Language:
English
Pubs id:
1237023
Local pid:
pubs:1237023
Source identifiers:
W4206119050
Deposit date:
2026-04-09
ARK identifier:

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