MAIT cells detect and efficiently lyse bacterially-infected epithelial cells
Mucosal associated invariant T cells (MAIT) are innate T lymphocytes that detect a large variety of bacteria and yeasts. This recognition depends on the detection of microbial compounds presented by the evolutionarily conserved major-histocompatibility-complex (MHC) class I molecule, MR1. Here we sh...
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creator | Le Bourhis, Lionel Dusseaux, Mathilde Bohineust, Armelle Bessoles, Stéphanie Martin, Emmanuel Premel, Virginie Coré, Maxime Sleurs, David Serriari, Nacer-Eddine Treiner, Emmanuel Hivroz, Claire Sansonetti, Philippe Gougeon, Marie-Lise Soudais, Claire Lantz, Olivier |
description | Mucosal associated invariant T cells (MAIT) are innate T lymphocytes that detect a large variety of bacteria and yeasts. This recognition depends on the detection of microbial compounds presented by the evolutionarily conserved major-histocompatibility-complex (MHC) class I molecule, MR1. Here we show that MAIT cells display cytotoxic activity towards MR1 overexpressing non-hematopoietic cells cocultured with bacteria. The NK receptor, CD161, highly expressed by MAIT cells, modulated the cytokine but not the cytotoxic response triggered by bacteria infected cells. MAIT cells are also activated by and kill epithelial cells expressing endogenous levels of MRI after infection with the invasive bacteria Shigella flexneri. In contrast, MAIT cells were not activated by epithelial cells infected by Salmonella enterica Typhimurium. Finally, MAIT cells are activated in human volunteers receiving an attenuated strain of Shigella dysenteriae-1 tested as a potential vaccine. Thus, in humans, MAIT cells are the most abundant T cell subset able to detect and kill bacteria infected cells. |
doi_str_mv | 10.1371/journal.ppat.1003681 |
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This recognition depends on the detection of microbial compounds presented by the evolutionarily conserved major-histocompatibility-complex (MHC) class I molecule, MR1. Here we show that MAIT cells display cytotoxic activity towards MR1 overexpressing non-hematopoietic cells cocultured with bacteria. The NK receptor, CD161, highly expressed by MAIT cells, modulated the cytokine but not the cytotoxic response triggered by bacteria infected cells. MAIT cells are also activated by and kill epithelial cells expressing endogenous levels of MRI after infection with the invasive bacteria Shigella flexneri. In contrast, MAIT cells were not activated by epithelial cells infected by Salmonella enterica Typhimurium. Finally, MAIT cells are activated in human volunteers receiving an attenuated strain of Shigella dysenteriae-1 tested as a potential vaccine. Thus, in humans, MAIT cells are the most abundant T cell subset able to detect and kill bacteria infected cells.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1003681</identifier><identifier>PMID: 24130485</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Bacteria ; Bacterial infections ; Bacteriology ; Cytotoxicity ; Dysentery, Bacillary - immunology ; Dysentery, Bacillary - pathology ; Epithelial cells ; Epithelial Cells - immunology ; Epithelial Cells - microbiology ; Epithelial Cells - pathology ; Experiments ; Female ; Genetic aspects ; Health aspects ; Histocompatibility Antigens Class I - immunology ; Host-parasite relationships ; Humans ; Immunity, Mucosal ; Intestinal Mucosa - immunology ; Intestinal Mucosa - microbiology ; Intestinal Mucosa - pathology ; Life Sciences ; Lymphocytes ; Major histocompatibility complex ; Male ; Microbiology ; Minor Histocompatibility Antigens ; NK Cell Lectin-Like Receptor Subfamily B - immunology ; Physiological aspects ; Salmonella ; Salmonella Infections - immunology ; Salmonella Infections - pathology ; Salmonella typhimurium - immunology ; Shigella dysenteriae - immunology ; Software ; T-Lymphocytes - immunology ; T-Lymphocytes - pathology</subject><ispartof>PLoS pathogens, 2013-10, Vol.9 (10), p.e1003681-e1003681</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>Attribution</rights><rights>2013 Le Bourhis et al 2013 Le Bourhis et al</rights><rights>2013 Le Bourhis et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Le Bourhis L, Dusseaux M, Bohineust A, Bessoles S, Martin E, et al. (2013) MAIT Cells Detect and Efficiently Lyse Bacterially-Infected Epithelial Cells. 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This recognition depends on the detection of microbial compounds presented by the evolutionarily conserved major-histocompatibility-complex (MHC) class I molecule, MR1. Here we show that MAIT cells display cytotoxic activity towards MR1 overexpressing non-hematopoietic cells cocultured with bacteria. The NK receptor, CD161, highly expressed by MAIT cells, modulated the cytokine but not the cytotoxic response triggered by bacteria infected cells. MAIT cells are also activated by and kill epithelial cells expressing endogenous levels of MRI after infection with the invasive bacteria Shigella flexneri. In contrast, MAIT cells were not activated by epithelial cells infected by Salmonella enterica Typhimurium. Finally, MAIT cells are activated in human volunteers receiving an attenuated strain of Shigella dysenteriae-1 tested as a potential vaccine. Thus, in humans, MAIT cells are the most abundant T cell subset able to detect and kill bacteria infected cells.</description><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Bacteriology</subject><subject>Cytotoxicity</subject><subject>Dysentery, Bacillary - immunology</subject><subject>Dysentery, Bacillary - pathology</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - immunology</subject><subject>Epithelial Cells - microbiology</subject><subject>Epithelial Cells - pathology</subject><subject>Experiments</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Histocompatibility Antigens Class I - immunology</subject><subject>Host-parasite relationships</subject><subject>Humans</subject><subject>Immunity, Mucosal</subject><subject>Intestinal Mucosa - immunology</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Intestinal Mucosa - pathology</subject><subject>Life Sciences</subject><subject>Lymphocytes</subject><subject>Major histocompatibility complex</subject><subject>Male</subject><subject>Microbiology</subject><subject>Minor Histocompatibility Antigens</subject><subject>NK Cell Lectin-Like Receptor Subfamily B - immunology</subject><subject>Physiological aspects</subject><subject>Salmonella</subject><subject>Salmonella Infections - immunology</subject><subject>Salmonella Infections - pathology</subject><subject>Salmonella typhimurium - immunology</subject><subject>Shigella dysenteriae - immunology</subject><subject>Software</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - pathology</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVkkGP0zAQhSMEYpeFf4AgEhf20GLHdm1fkKoVsJUKSLCcrYkzaV25SYnTFf33TEh3tUVcUA6xJt97E7-ZLHvJ2ZQLzd9t2n3XQJzudtBPOWNiZvij7JwrJSZaaPn4wfkse5bShjHJBZ89zc4KOjBp1Hm2_Dxf3OQeY0x5hT36PoemyrGugw_Y9PGQx0PCvATfYxcgxsMkNDVxSNQu9GuMVB0dnmdPaogJXxzfF9mPjx9urq4ny6-fFlfz5cRrIfqJKLjA2tZWW2ErMJLNaiuLooCigkIpYw0IDwbBUF2WFddoLLKyshzKEsRF9nr03cU2uWMQyXFJUjJXmojFSFQtbNyuC1voDq6F4P4U2m7loOuDj-h0WSlhjQEJXjI2K_WMwgTOmSqR2Yq83h-77cstVp5S6SCemJ5-acLardpbJ7RVNBYyuBwN1n_JrudLN9SYUFZrzW45sW-Pzbr25x5T77YhDeFCg-1-uKOkn2TcMELfjOgK6Bo0lJa6-wF3c6G4lUoxQ9T0HxQ9FW6DbxusA9VPBJcnAmJ6_NWvYJ-SW3z_9h_sl1NWjqzv2pQ6rO-j4MwNG303SDdstDtuNMlePUz_XnS3wuI3YaHwJQ</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>Le Bourhis, Lionel</creator><creator>Dusseaux, Mathilde</creator><creator>Bohineust, Armelle</creator><creator>Bessoles, Stéphanie</creator><creator>Martin, Emmanuel</creator><creator>Premel, Virginie</creator><creator>Coré, Maxime</creator><creator>Sleurs, David</creator><creator>Serriari, Nacer-Eddine</creator><creator>Treiner, Emmanuel</creator><creator>Hivroz, Claire</creator><creator>Sansonetti, Philippe</creator><creator>Gougeon, Marie-Lise</creator><creator>Soudais, Claire</creator><creator>Lantz, Olivier</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7542-4527</orcidid><orcidid>https://orcid.org/0000-0003-3161-7719</orcidid><orcidid>https://orcid.org/0000-0002-6794-2890</orcidid><orcidid>https://orcid.org/0000-0003-3878-8633</orcidid><orcidid>https://orcid.org/0000-0003-4211-7373</orcidid></search><sort><creationdate>20131001</creationdate><title>MAIT cells detect and efficiently lyse bacterially-infected epithelial cells</title><author>Le Bourhis, Lionel ; Dusseaux, Mathilde ; Bohineust, Armelle ; Bessoles, Stéphanie ; Martin, Emmanuel ; Premel, Virginie ; Coré, Maxime ; Sleurs, David ; Serriari, Nacer-Eddine ; Treiner, Emmanuel ; Hivroz, Claire ; Sansonetti, Philippe ; Gougeon, Marie-Lise ; Soudais, Claire ; Lantz, Olivier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c733t-3213ef9f97939da8406f94222a2da255898a3ca8ea8f944bd17e89e0bd91abba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Bacteria</topic><topic>Bacterial infections</topic><topic>Bacteriology</topic><topic>Cytotoxicity</topic><topic>Dysentery, Bacillary - immunology</topic><topic>Dysentery, Bacillary - pathology</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - immunology</topic><topic>Epithelial Cells - microbiology</topic><topic>Epithelial Cells - pathology</topic><topic>Experiments</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Histocompatibility Antigens Class I - immunology</topic><topic>Host-parasite relationships</topic><topic>Humans</topic><topic>Immunity, Mucosal</topic><topic>Intestinal Mucosa - immunology</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Intestinal Mucosa - pathology</topic><topic>Life Sciences</topic><topic>Lymphocytes</topic><topic>Major histocompatibility complex</topic><topic>Male</topic><topic>Microbiology</topic><topic>Minor Histocompatibility Antigens</topic><topic>NK Cell Lectin-Like Receptor Subfamily B - immunology</topic><topic>Physiological aspects</topic><topic>Salmonella</topic><topic>Salmonella Infections - immunology</topic><topic>Salmonella Infections - pathology</topic><topic>Salmonella typhimurium - immunology</topic><topic>Shigella dysenteriae - immunology</topic><topic>Software</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le Bourhis, Lionel</creatorcontrib><creatorcontrib>Dusseaux, Mathilde</creatorcontrib><creatorcontrib>Bohineust, Armelle</creatorcontrib><creatorcontrib>Bessoles, Stéphanie</creatorcontrib><creatorcontrib>Martin, Emmanuel</creatorcontrib><creatorcontrib>Premel, Virginie</creatorcontrib><creatorcontrib>Coré, Maxime</creatorcontrib><creatorcontrib>Sleurs, David</creatorcontrib><creatorcontrib>Serriari, Nacer-Eddine</creatorcontrib><creatorcontrib>Treiner, Emmanuel</creatorcontrib><creatorcontrib>Hivroz, Claire</creatorcontrib><creatorcontrib>Sansonetti, Philippe</creatorcontrib><creatorcontrib>Gougeon, Marie-Lise</creatorcontrib><creatorcontrib>Soudais, Claire</creatorcontrib><creatorcontrib>Lantz, Olivier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le Bourhis, Lionel</au><au>Dusseaux, Mathilde</au><au>Bohineust, Armelle</au><au>Bessoles, Stéphanie</au><au>Martin, Emmanuel</au><au>Premel, Virginie</au><au>Coré, Maxime</au><au>Sleurs, David</au><au>Serriari, Nacer-Eddine</au><au>Treiner, Emmanuel</au><au>Hivroz, Claire</au><au>Sansonetti, Philippe</au><au>Gougeon, Marie-Lise</au><au>Soudais, Claire</au><au>Lantz, Olivier</au><au>DeLeo, Frank R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MAIT cells detect and efficiently lyse bacterially-infected epithelial cells</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2013-10-01</date><risdate>2013</risdate><volume>9</volume><issue>10</issue><spage>e1003681</spage><epage>e1003681</epage><pages>e1003681-e1003681</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Mucosal associated invariant T cells (MAIT) are innate T lymphocytes that detect a large variety of bacteria and yeasts. This recognition depends on the detection of microbial compounds presented by the evolutionarily conserved major-histocompatibility-complex (MHC) class I molecule, MR1. Here we show that MAIT cells display cytotoxic activity towards MR1 overexpressing non-hematopoietic cells cocultured with bacteria. The NK receptor, CD161, highly expressed by MAIT cells, modulated the cytokine but not the cytotoxic response triggered by bacteria infected cells. MAIT cells are also activated by and kill epithelial cells expressing endogenous levels of MRI after infection with the invasive bacteria Shigella flexneri. In contrast, MAIT cells were not activated by epithelial cells infected by Salmonella enterica Typhimurium. Finally, MAIT cells are activated in human volunteers receiving an attenuated strain of Shigella dysenteriae-1 tested as a potential vaccine. 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subjects | Bacteria Bacterial infections Bacteriology Cytotoxicity Dysentery, Bacillary - immunology Dysentery, Bacillary - pathology Epithelial cells Epithelial Cells - immunology Epithelial Cells - microbiology Epithelial Cells - pathology Experiments Female Genetic aspects Health aspects Histocompatibility Antigens Class I - immunology Host-parasite relationships Humans Immunity, Mucosal Intestinal Mucosa - immunology Intestinal Mucosa - microbiology Intestinal Mucosa - pathology Life Sciences Lymphocytes Major histocompatibility complex Male Microbiology Minor Histocompatibility Antigens NK Cell Lectin-Like Receptor Subfamily B - immunology Physiological aspects Salmonella Salmonella Infections - immunology Salmonella Infections - pathology Salmonella typhimurium - immunology Shigella dysenteriae - immunology Software T-Lymphocytes - immunology T-Lymphocytes - pathology |
title | MAIT cells detect and efficiently lyse bacterially-infected epithelial cells |
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