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MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A
Mucosal-associated invariant T (MAIT) cells are innate-like T cells that can detect bacteria-derived metabolites presented on MR1. Here we show, using a controlled infection of humans with live Salmonella enterica serovar Paratyphi A, that MAIT cells are activated during infection, an effect maintai...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772558/ https://www.ncbi.nlm.nih.gov/pubmed/29343684 http://dx.doi.org/10.1038/s41467-017-02540-x |
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author | Howson, Lauren J. Napolitani, Giorgio Shepherd, Dawn Ghadbane, Hemza Kurupati, Prathiba Preciado-Llanes, Lorena Rei, Margarida Dobinson, Hazel C. Gibani, Malick M. Teng, Karen Wei Weng Newell, Evan W. Veerapen, Natacha Besra, Gurdyal S. Pollard, Andrew J. Cerundolo, Vincenzo |
author_facet | Howson, Lauren J. Napolitani, Giorgio Shepherd, Dawn Ghadbane, Hemza Kurupati, Prathiba Preciado-Llanes, Lorena Rei, Margarida Dobinson, Hazel C. Gibani, Malick M. Teng, Karen Wei Weng Newell, Evan W. Veerapen, Natacha Besra, Gurdyal S. Pollard, Andrew J. Cerundolo, Vincenzo |
author_sort | Howson, Lauren J. |
collection | PubMed |
description | Mucosal-associated invariant T (MAIT) cells are innate-like T cells that can detect bacteria-derived metabolites presented on MR1. Here we show, using a controlled infection of humans with live Salmonella enterica serovar Paratyphi A, that MAIT cells are activated during infection, an effect maintained even after antibiotic treatment. At the peak of infection MAIT cell T-cell receptor (TCR)β clonotypes that are over-represented prior to infection transiently contract. Select MAIT cell TCRβ clonotypes that expand after infection have stronger TCR-dependent activation than do contracted clonotypes. Our results demonstrate that host exposure to antigen may drive clonal expansion of MAIT cells with increased functional avidity, suggesting a role for specific vaccination strategies to increase the frequency and potency of MAIT cells to optimize effector function. |
format | Online Article Text |
id | pubmed-5772558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57725582018-01-23 MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A Howson, Lauren J. Napolitani, Giorgio Shepherd, Dawn Ghadbane, Hemza Kurupati, Prathiba Preciado-Llanes, Lorena Rei, Margarida Dobinson, Hazel C. Gibani, Malick M. Teng, Karen Wei Weng Newell, Evan W. Veerapen, Natacha Besra, Gurdyal S. Pollard, Andrew J. Cerundolo, Vincenzo Nat Commun Article Mucosal-associated invariant T (MAIT) cells are innate-like T cells that can detect bacteria-derived metabolites presented on MR1. Here we show, using a controlled infection of humans with live Salmonella enterica serovar Paratyphi A, that MAIT cells are activated during infection, an effect maintained even after antibiotic treatment. At the peak of infection MAIT cell T-cell receptor (TCR)β clonotypes that are over-represented prior to infection transiently contract. Select MAIT cell TCRβ clonotypes that expand after infection have stronger TCR-dependent activation than do contracted clonotypes. Our results demonstrate that host exposure to antigen may drive clonal expansion of MAIT cells with increased functional avidity, suggesting a role for specific vaccination strategies to increase the frequency and potency of MAIT cells to optimize effector function. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772558/ /pubmed/29343684 http://dx.doi.org/10.1038/s41467-017-02540-x Text en © The Author(s) 2018 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 Howson, Lauren J. Napolitani, Giorgio Shepherd, Dawn Ghadbane, Hemza Kurupati, Prathiba Preciado-Llanes, Lorena Rei, Margarida Dobinson, Hazel C. Gibani, Malick M. Teng, Karen Wei Weng Newell, Evan W. Veerapen, Natacha Besra, Gurdyal S. Pollard, Andrew J. Cerundolo, Vincenzo MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title_full | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title_fullStr | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title_full_unstemmed | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title_short | MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A |
title_sort | mait cell clonal expansion and tcr repertoire shaping in human volunteers challenged with salmonella paratyphi a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772558/ https://www.ncbi.nlm.nih.gov/pubmed/29343684 http://dx.doi.org/10.1038/s41467-017-02540-x |
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