Journal article
MAIT cells: new guardians of the liver
- Abstract:
- The liver is an important immunological organ that remains sterile and tolerogenic in homeostasis, despite continual exposure to non-self food and microbial-derived products from the gut. However, where intestinal mucosal defenses are breached or in the presence of a systemic infection, the liver acts as a second 'firewall', because of its enrichment with innate effector cells able to rapidly respond to infections or tissue dysregulation. One of the largest populations of T cells within the human liver are mucosal-associated invariant T (MAIT) cells, a novel innate-like T-cell population that can recognize a highly conserved antigen derived from the microbial riboflavin synthesis pathway. MAIT cells are emerging as significant players in the human immune system, associated with an increasing number of clinical diseases of bacterial, viral, autoimmune and cancerous origin. As reviewed here, we are only beginning to investigate the potential role of this dominant T-cell subset in the liver, but the reactivity of MAIT cells to both inflammatory cytokines and riboflavin derivatives suggests that MAIT cells may have an important role in first line of defense as part of the liver firewall. As such, MAIT cells are promising targets for modulating the host defense and inflammation in both acute and chronic liver diseases.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.8MB, Terms of use)
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- Publisher copy:
- 10.1038/cti.2016.51
Authors
- Publisher:
- Nature Publishing Group
- Journal:
- Clinical & translational immunology More from this journal
- Volume:
- 5
- Issue:
- 8
- Pages:
- e98
- Publication date:
- 2016-08-19
- Acceptance date:
- 2016-07-15
- DOI:
- EISSN:
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2050-0068
- Pmid:
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27588203
- Language:
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English
- Keywords:
- Pubs id:
-
pubs:641848
- UUID:
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uuid:f85123c0-f18f-4936-a0f9-4bcb38f0f979
- Local pid:
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pubs:641848
- Source identifiers:
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641848
- Deposit date:
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2016-09-21
- ARK identifier:
Terms of use
- Copyright holder:
- Kurioka, et al
- Copyright date:
- 2016
- Notes:
- © The Authors. Published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
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