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
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 5.0MB, Terms of use)
-
- Publisher copy:
- 10.1136/gutjnl-2021-324478
Authors
+ Swiss National Science Foundation
More from this funder
- Funder identifier:
- https://ror.org/00yjd3n13
- Grant:
- PZ00P3_189490
- PZ00P3_167828
+ NIHR Oxford Musculoskeletal Biomedical Research Centre
More from this funder
- Funder identifier:
- https://ror.org/00aps1a34
- 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:
Terms of use
- Copyright holder:
- Lett et al.
- Copyright date:
- 2022
- Rights statement:
- © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC.
If you are the owner of this record, you can report an update to it here: Report update to this record