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Diverse MR1-restricted T cells in mice and humans
Mucosal-associated invariant T (MAIT) cells express an invariant TRAV1/TRAJ33 TCR-α chain and are restricted to the MHC-I-like molecule, MR1. Whether MAIT cell development depends on this invariant TCR-α chain is unclear. Here we generate Traj33-deficient mice and show that they are highly depleted...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529461/ https://www.ncbi.nlm.nih.gov/pubmed/31113973 http://dx.doi.org/10.1038/s41467-019-10198-w |
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author | Koay, Hui-Fern Gherardin, Nicholas A. Xu, Calvin Seneviratna, Rebecca Zhao, Zhe Chen, Zhenjun Fairlie, David P. McCluskey, James Pellicci, Daniel G. Uldrich, Adam P. Godfrey, Dale I. |
author_facet | Koay, Hui-Fern Gherardin, Nicholas A. Xu, Calvin Seneviratna, Rebecca Zhao, Zhe Chen, Zhenjun Fairlie, David P. McCluskey, James Pellicci, Daniel G. Uldrich, Adam P. Godfrey, Dale I. |
author_sort | Koay, Hui-Fern |
collection | PubMed |
description | Mucosal-associated invariant T (MAIT) cells express an invariant TRAV1/TRAJ33 TCR-α chain and are restricted to the MHC-I-like molecule, MR1. Whether MAIT cell development depends on this invariant TCR-α chain is unclear. Here we generate Traj33-deficient mice and show that they are highly depleted of MAIT cells; however, a residual population remains and can respond to exogenous antigen in vitro or pulmonary Legionella challenge in vivo. These residual cells include some that express Trav1(+) TCRs with conservative Traj-gene substitutions, and others that express Trav1(-) TCRs with a broad range of Traj genes. We further report that human TRAV1-2(-) MR1-restricted T cells contain both MAIT-like and non-MAIT-like cells, as judged by their TCR repertoire, antigen reactivity and phenotypic features. These include a MAIT-like population that expresses a public, canonical TRAV36(+) TRBV28(+) TCR. Our findings highlight the TCR diversity and the resulting potential impact on antigen recognition by MR1-restricted T cells. |
format | Online Article Text |
id | pubmed-6529461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65294612019-05-23 Diverse MR1-restricted T cells in mice and humans Koay, Hui-Fern Gherardin, Nicholas A. Xu, Calvin Seneviratna, Rebecca Zhao, Zhe Chen, Zhenjun Fairlie, David P. McCluskey, James Pellicci, Daniel G. Uldrich, Adam P. Godfrey, Dale I. Nat Commun Article Mucosal-associated invariant T (MAIT) cells express an invariant TRAV1/TRAJ33 TCR-α chain and are restricted to the MHC-I-like molecule, MR1. Whether MAIT cell development depends on this invariant TCR-α chain is unclear. Here we generate Traj33-deficient mice and show that they are highly depleted of MAIT cells; however, a residual population remains and can respond to exogenous antigen in vitro or pulmonary Legionella challenge in vivo. These residual cells include some that express Trav1(+) TCRs with conservative Traj-gene substitutions, and others that express Trav1(-) TCRs with a broad range of Traj genes. We further report that human TRAV1-2(-) MR1-restricted T cells contain both MAIT-like and non-MAIT-like cells, as judged by their TCR repertoire, antigen reactivity and phenotypic features. These include a MAIT-like population that expresses a public, canonical TRAV36(+) TRBV28(+) TCR. Our findings highlight the TCR diversity and the resulting potential impact on antigen recognition by MR1-restricted T cells. Nature Publishing Group UK 2019-05-21 /pmc/articles/PMC6529461/ /pubmed/31113973 http://dx.doi.org/10.1038/s41467-019-10198-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Koay, Hui-Fern Gherardin, Nicholas A. Xu, Calvin Seneviratna, Rebecca Zhao, Zhe Chen, Zhenjun Fairlie, David P. McCluskey, James Pellicci, Daniel G. Uldrich, Adam P. Godfrey, Dale I. Diverse MR1-restricted T cells in mice and humans |
title | Diverse MR1-restricted T cells in mice and humans |
title_full | Diverse MR1-restricted T cells in mice and humans |
title_fullStr | Diverse MR1-restricted T cells in mice and humans |
title_full_unstemmed | Diverse MR1-restricted T cells in mice and humans |
title_short | Diverse MR1-restricted T cells in mice and humans |
title_sort | diverse mr1-restricted t cells in mice and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529461/ https://www.ncbi.nlm.nih.gov/pubmed/31113973 http://dx.doi.org/10.1038/s41467-019-10198-w |
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