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Mucosal Associated Invariant T Cells in Cancer-Friend or Foe?
SIMPLE SUMMARY: Mucosal associated invariant T (MAIT) cells are a population of innate T cells which play an important role in host protection against bacterial, fungi and viruses. MAIT cells are armed with potent cytotoxic machinery, allowing them to kill invading pathogens but also transformed cel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036566/ https://www.ncbi.nlm.nih.gov/pubmed/33808058 http://dx.doi.org/10.3390/cancers13071582 |
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author | O’Neill, Chloe Cassidy, Féaron C. O’Shea, Donal Hogan, Andrew E. |
author_facet | O’Neill, Chloe Cassidy, Féaron C. O’Shea, Donal Hogan, Andrew E. |
author_sort | O’Neill, Chloe |
collection | PubMed |
description | SIMPLE SUMMARY: Mucosal associated invariant T (MAIT) cells are a population of innate T cells which play an important role in host protection against bacterial, fungi and viruses. MAIT cells are armed with potent cytotoxic machinery, allowing them to kill invading pathogens but also transformed cells. Many studies have investigated MAIT cells in the setting of various human cancers, with conflicting results. Several studies have identified MAIT cells as potent anti-cancer effector cells, whilst others have reported a potential pathogenic role for MAIT cells in certain cancers. In this review, we discuss the current knowledge base and highlight potential mechanisms which may underpin the reported cancer-related alterations in MAIT cells. ABSTRACT: Mucosal associated invariant T (MAIT) cells are a population of unconventional T cells which can bridge the innate and adaptive immune systems. Well-described roles for MAIT cells include host protection against invading bacteria, fungi and viruses. Upon activation, MAIT cells become prolific effector cells, capable of producing a range of cytokines and lytic molecules. In addition to their anti-microbial role, MAIT cells have been implicated in immune responses to cancer, with opposing beneficial and pathogenic roles reported. On the one hand, MAIT cells can home to the site of the tumour in many human cancers and can produce anti-tumour molecules. On the other, MAIT cells can display defective phenotypes in certain cancers and produce pro-tumour molecules. In this review, we discuss the current literature on the diverse roles for MAIT cells in cancer, outlining their frequencies, functions and associations with N staging and prognosis. We also discuss potential mechanisms underpinning cancer-related alterations in MAIT cells and highlight therapeutic approaches to harness or target MAIT cells in cancer. |
format | Online Article Text |
id | pubmed-8036566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80365662021-04-12 Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? O’Neill, Chloe Cassidy, Féaron C. O’Shea, Donal Hogan, Andrew E. Cancers (Basel) Review SIMPLE SUMMARY: Mucosal associated invariant T (MAIT) cells are a population of innate T cells which play an important role in host protection against bacterial, fungi and viruses. MAIT cells are armed with potent cytotoxic machinery, allowing them to kill invading pathogens but also transformed cells. Many studies have investigated MAIT cells in the setting of various human cancers, with conflicting results. Several studies have identified MAIT cells as potent anti-cancer effector cells, whilst others have reported a potential pathogenic role for MAIT cells in certain cancers. In this review, we discuss the current knowledge base and highlight potential mechanisms which may underpin the reported cancer-related alterations in MAIT cells. ABSTRACT: Mucosal associated invariant T (MAIT) cells are a population of unconventional T cells which can bridge the innate and adaptive immune systems. Well-described roles for MAIT cells include host protection against invading bacteria, fungi and viruses. Upon activation, MAIT cells become prolific effector cells, capable of producing a range of cytokines and lytic molecules. In addition to their anti-microbial role, MAIT cells have been implicated in immune responses to cancer, with opposing beneficial and pathogenic roles reported. On the one hand, MAIT cells can home to the site of the tumour in many human cancers and can produce anti-tumour molecules. On the other, MAIT cells can display defective phenotypes in certain cancers and produce pro-tumour molecules. In this review, we discuss the current literature on the diverse roles for MAIT cells in cancer, outlining their frequencies, functions and associations with N staging and prognosis. We also discuss potential mechanisms underpinning cancer-related alterations in MAIT cells and highlight therapeutic approaches to harness or target MAIT cells in cancer. MDPI 2021-03-30 /pmc/articles/PMC8036566/ /pubmed/33808058 http://dx.doi.org/10.3390/cancers13071582 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Review O’Neill, Chloe Cassidy, Féaron C. O’Shea, Donal Hogan, Andrew E. Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title | Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title_full | Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title_fullStr | Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title_full_unstemmed | Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title_short | Mucosal Associated Invariant T Cells in Cancer-Friend or Foe? |
title_sort | mucosal associated invariant t cells in cancer-friend or foe? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036566/ https://www.ncbi.nlm.nih.gov/pubmed/33808058 http://dx.doi.org/10.3390/cancers13071582 |
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