Cargando…
MR1-Restricted T Cells Are Unprecedented Cancer Fighters
Non-polymorphic MHC class I-related molecule MR1 presents antigenic bacterial metabolites to mucosal-associated invariant T (MAIT) cells and self-antigens to MR1-restricted T (MR1T) cells. Both MR1-restricted T cell populations are readily identified in healthy individuals, with MAIT cells accountin...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198878/ https://www.ncbi.nlm.nih.gov/pubmed/32411144 http://dx.doi.org/10.3389/fimmu.2020.00751 |
_version_ | 1783529077849718784 |
---|---|
author | Vacchini, Alessandro Chancellor, Andrew Spagnuolo, Julian Mori, Lucia De Libero, Gennaro |
author_facet | Vacchini, Alessandro Chancellor, Andrew Spagnuolo, Julian Mori, Lucia De Libero, Gennaro |
author_sort | Vacchini, Alessandro |
collection | PubMed |
description | Non-polymorphic MHC class I-related molecule MR1 presents antigenic bacterial metabolites to mucosal-associated invariant T (MAIT) cells and self-antigens to MR1-restricted T (MR1T) cells. Both MR1-restricted T cell populations are readily identified in healthy individuals, with MAIT cells accounting for 1–10% of circulating T cells, while MR1T cells have frequencies comparable to peptide-specific T cells (<0.1%). Self-reactive MR1T cells display a heterogeneous phenotype, and are capable of releasing both T(H1) and T(H2) cytokines, supporting not only activation of inflammation but also contributing to its regulation. Importantly, MR1T cells recognize and kill a diverse range of MR1-expressing tumor cells. On the other hand, evidence suggests MAIT cells augment cancer growth and metastases. This review addresses the potential role of MR1-restricted T cells in controlling tumor cells, facilitating their elimination and regulating cancer immunity. We also discuss therapeutic opportunities surrounding MR1-restricted T cells in cancer. |
format | Online Article Text |
id | pubmed-7198878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71988782020-05-14 MR1-Restricted T Cells Are Unprecedented Cancer Fighters Vacchini, Alessandro Chancellor, Andrew Spagnuolo, Julian Mori, Lucia De Libero, Gennaro Front Immunol Immunology Non-polymorphic MHC class I-related molecule MR1 presents antigenic bacterial metabolites to mucosal-associated invariant T (MAIT) cells and self-antigens to MR1-restricted T (MR1T) cells. Both MR1-restricted T cell populations are readily identified in healthy individuals, with MAIT cells accounting for 1–10% of circulating T cells, while MR1T cells have frequencies comparable to peptide-specific T cells (<0.1%). Self-reactive MR1T cells display a heterogeneous phenotype, and are capable of releasing both T(H1) and T(H2) cytokines, supporting not only activation of inflammation but also contributing to its regulation. Importantly, MR1T cells recognize and kill a diverse range of MR1-expressing tumor cells. On the other hand, evidence suggests MAIT cells augment cancer growth and metastases. This review addresses the potential role of MR1-restricted T cells in controlling tumor cells, facilitating their elimination and regulating cancer immunity. We also discuss therapeutic opportunities surrounding MR1-restricted T cells in cancer. Frontiers Media S.A. 2020-04-28 /pmc/articles/PMC7198878/ /pubmed/32411144 http://dx.doi.org/10.3389/fimmu.2020.00751 Text en Copyright © 2020 Vacchini, Chancellor, Spagnuolo, Mori and De Libero. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Vacchini, Alessandro Chancellor, Andrew Spagnuolo, Julian Mori, Lucia De Libero, Gennaro MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title | MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title_full | MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title_fullStr | MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title_full_unstemmed | MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title_short | MR1-Restricted T Cells Are Unprecedented Cancer Fighters |
title_sort | mr1-restricted t cells are unprecedented cancer fighters |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198878/ https://www.ncbi.nlm.nih.gov/pubmed/32411144 http://dx.doi.org/10.3389/fimmu.2020.00751 |
work_keys_str_mv | AT vacchinialessandro mr1restrictedtcellsareunprecedentedcancerfighters AT chancellorandrew mr1restrictedtcellsareunprecedentedcancerfighters AT spagnuolojulian mr1restrictedtcellsareunprecedentedcancerfighters AT morilucia mr1restrictedtcellsareunprecedentedcancerfighters AT deliberogennaro mr1restrictedtcellsareunprecedentedcancerfighters |