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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...

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Autores principales: Dias, Joana, Sobkowiak, Michał J., Sandberg, Johan K., Leeansyah, Edwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Leukocyte Biology 2016
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.
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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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