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MR1, an immunological periscope of cellular metabolism

The discovery that major histocompatibility complex (MHC) class I-related molecule 1 (MR1) presents microbial antigens to mucosal-associated invariant T (MAIT) cells was a significant scientific milestone in the last decade. Surveillance for foreign metabolically derived antigens added a new class o...

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Detalles Bibliográficos
Autores principales: Chancellor, Andrew, Vacchini, Alessandro, De Libero, Gennaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865192/
https://www.ncbi.nlm.nih.gov/pubmed/34718585
http://dx.doi.org/10.1093/intimm/dxab101
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author Chancellor, Andrew
Vacchini, Alessandro
De Libero, Gennaro
author_facet Chancellor, Andrew
Vacchini, Alessandro
De Libero, Gennaro
author_sort Chancellor, Andrew
collection PubMed
description The discovery that major histocompatibility complex (MHC) class I-related molecule 1 (MR1) presents microbial antigens to mucosal-associated invariant T (MAIT) cells was a significant scientific milestone in the last decade. Surveillance for foreign metabolically derived antigens added a new class of target structures for immune recognition. The recent identification of a second family of MR1-restricted T cells, called MR1T cells, which show self-reactivity suggests the microbial antigens characterized so far may only represent a handful of the potential structures presented by MR1. Furthermore, the reactivity of MR1T cells towards tumours and not healthy cells indicates tight regulation in the generation of self-antigens and in MR1 expression and antigen loading. These novel and exciting observations invite consideration of new perspectives of MR1-restricted antigen presentation and its wider role within immunity and disease.
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spelling pubmed-88651922022-02-24 MR1, an immunological periscope of cellular metabolism Chancellor, Andrew Vacchini, Alessandro De Libero, Gennaro Int Immunol Invited Reviews The discovery that major histocompatibility complex (MHC) class I-related molecule 1 (MR1) presents microbial antigens to mucosal-associated invariant T (MAIT) cells was a significant scientific milestone in the last decade. Surveillance for foreign metabolically derived antigens added a new class of target structures for immune recognition. The recent identification of a second family of MR1-restricted T cells, called MR1T cells, which show self-reactivity suggests the microbial antigens characterized so far may only represent a handful of the potential structures presented by MR1. Furthermore, the reactivity of MR1T cells towards tumours and not healthy cells indicates tight regulation in the generation of self-antigens and in MR1 expression and antigen loading. These novel and exciting observations invite consideration of new perspectives of MR1-restricted antigen presentation and its wider role within immunity and disease. Oxford University Press 2021-10-27 /pmc/articles/PMC8865192/ /pubmed/34718585 http://dx.doi.org/10.1093/intimm/dxab101 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Japanese Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Reviews
Chancellor, Andrew
Vacchini, Alessandro
De Libero, Gennaro
MR1, an immunological periscope of cellular metabolism
title MR1, an immunological periscope of cellular metabolism
title_full MR1, an immunological periscope of cellular metabolism
title_fullStr MR1, an immunological periscope of cellular metabolism
title_full_unstemmed MR1, an immunological periscope of cellular metabolism
title_short MR1, an immunological periscope of cellular metabolism
title_sort mr1, an immunological periscope of cellular metabolism
topic Invited Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865192/
https://www.ncbi.nlm.nih.gov/pubmed/34718585
http://dx.doi.org/10.1093/intimm/dxab101
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