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Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity
Mucosa-associated invariant T cells are a large and relatively recently described innate-like antimicrobial T-cell subset in humans. These cells recognize riboflavin metabolites from a range of microbes presented by evolutionarily conserved major histocompatibility complex, class I-related molecules...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Leukocyte Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946616/ https://www.ncbi.nlm.nih.gov/pubmed/27034405 http://dx.doi.org/10.1189/jlb.4TA0815-391RR |
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author | Dias, Joana Sobkowiak, Michał J. Sandberg, Johan K. Leeansyah, Edwin |
author_facet | Dias, Joana Sobkowiak, Michał J. Sandberg, Johan K. Leeansyah, Edwin |
author_sort | Dias, Joana |
collection | PubMed |
description | Mucosa-associated invariant T cells are a large and relatively recently described innate-like antimicrobial T-cell subset in humans. These cells recognize riboflavin metabolites from a range of microbes presented by evolutionarily conserved major histocompatibility complex, class I-related molecules. Given the innate-like characteristics of mucosa-associated invariant T cells and the novel type of antigens they recognize, new methodology must be developed and existing methods refined to allow comprehensive studies of their role in human immune defense against microbial infection. In this study, we established protocols to examine a range of mucosa-associated invariant T-cell functions as they respond to antigen produced by Escherichia coli. These improved and dose- and time-optimized experimental protocols allow detailed studies of MR1-dependent mucosa-associated invariant T-cell responses to Escherichia coli pulsed antigen-presenting cells, as assessed by expression of activation markers and cytokines, by proliferation, and by induction of apoptosis and death in major histocompatibility complex, class I-related–expressing target cells. The novel and optimized protocols establish a framework of methods and open new possibilities to study mucosa-associated invariant T-cell immunobiology, using Escherichia coli as a model antigen. Furthermore, we propose that these robust experimental systems can also be adapted to study mucosa-associated invariant T-cell responses to other microbes and types of antigen-presenting cells. |
format | Online Article Text |
id | pubmed-4946616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Society for Leukocyte Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-49466162016-07-18 Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity Dias, Joana Sobkowiak, Michał J. Sandberg, Johan K. Leeansyah, Edwin J Leukoc Biol Technical Advance Mucosa-associated invariant T cells are a large and relatively recently described innate-like antimicrobial T-cell subset in humans. These cells recognize riboflavin metabolites from a range of microbes presented by evolutionarily conserved major histocompatibility complex, class I-related molecules. Given the innate-like characteristics of mucosa-associated invariant T cells and the novel type of antigens they recognize, new methodology must be developed and existing methods refined to allow comprehensive studies of their role in human immune defense against microbial infection. In this study, we established protocols to examine a range of mucosa-associated invariant T-cell functions as they respond to antigen produced by Escherichia coli. These improved and dose- and time-optimized experimental protocols allow detailed studies of MR1-dependent mucosa-associated invariant T-cell responses to Escherichia coli pulsed antigen-presenting cells, as assessed by expression of activation markers and cytokines, by proliferation, and by induction of apoptosis and death in major histocompatibility complex, class I-related–expressing target cells. The novel and optimized protocols establish a framework of methods and open new possibilities to study mucosa-associated invariant T-cell immunobiology, using Escherichia coli as a model antigen. Furthermore, we propose that these robust experimental systems can also be adapted to study mucosa-associated invariant T-cell responses to other microbes and types of antigen-presenting cells. Society for Leukocyte Biology 2016-07 2016-03-31 /pmc/articles/PMC4946616/ /pubmed/27034405 http://dx.doi.org/10.1189/jlb.4TA0815-391RR Text en © The Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) (http://creativecommons.org/licenses/by-nc/4.0/) which permits noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Advance Dias, Joana Sobkowiak, Michał J. Sandberg, Johan K. Leeansyah, Edwin Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title | Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title_full | Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title_fullStr | Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title_full_unstemmed | Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title_short | Human MAIT-cell responses to Escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
title_sort | human mait-cell responses to escherichia coli: activation, cytokine production, proliferation, and cytotoxicity |
topic | Technical Advance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946616/ https://www.ncbi.nlm.nih.gov/pubmed/27034405 http://dx.doi.org/10.1189/jlb.4TA0815-391RR |
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