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Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity

Bacillus Calmette–Guérin (BCG) is used as a vaccine and diagnostic test for tuberculosis, as well as immunotherapy in the treatment of bladder cancer. While clinically useful, the response to mycobacterial stimulation is complex and the induced protein signature remains poorly defined. We characteri...

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Autores principales: Bisiaux, Aurélie, Boussier, Jeremy, Duffy, Darragh, Quintana-Murci, Lluis, Fontes, Magnus, Albert, Matthew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507989/
https://www.ncbi.nlm.nih.gov/pubmed/28751891
http://dx.doi.org/10.3389/fimmu.2017.00796
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author Bisiaux, Aurélie
Boussier, Jeremy
Duffy, Darragh
Quintana-Murci, Lluis
Fontes, Magnus
Albert, Matthew L.
author_facet Bisiaux, Aurélie
Boussier, Jeremy
Duffy, Darragh
Quintana-Murci, Lluis
Fontes, Magnus
Albert, Matthew L.
author_sort Bisiaux, Aurélie
collection PubMed
description Bacillus Calmette–Guérin (BCG) is used as a vaccine and diagnostic test for tuberculosis, as well as immunotherapy in the treatment of bladder cancer. While clinically useful, the response to mycobacterial stimulation is complex and the induced protein signature remains poorly defined. We characterized the cell types directly engaged by BCG, as well as the induced cytokine loops that transmit signal(s) to bystander cells. Standardized whole-blood stimulations and mechanistic studies on single and purified cell populations identified distinct patterns of activation in monocytes as compared to neutrophils and invariant lymphocyte populations. Deconvoluting the role of Toll-like receptor 2/4 and Dectin-1/2 in the inflammatory response to BCG, we revealed Dectin-1/2 as dominant in neutrophils as compared to monocytes, which equally engaged both pathways. Furthermore, we quantified the role of NF-κB and NADPH/reactive oxygen species (ROS)-dependent cytokines, which triggered a JAK1/2-dependent amplification loop and accounted for 40–50% of the induced response to BCG. In sum, this study provides new insight into the molecular and cellular pathways involved in the response to BCG, establishing the basis for a new generation of immunodiagnostic tools.
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spelling pubmed-55079892017-07-27 Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity Bisiaux, Aurélie Boussier, Jeremy Duffy, Darragh Quintana-Murci, Lluis Fontes, Magnus Albert, Matthew L. Front Immunol Immunology Bacillus Calmette–Guérin (BCG) is used as a vaccine and diagnostic test for tuberculosis, as well as immunotherapy in the treatment of bladder cancer. While clinically useful, the response to mycobacterial stimulation is complex and the induced protein signature remains poorly defined. We characterized the cell types directly engaged by BCG, as well as the induced cytokine loops that transmit signal(s) to bystander cells. Standardized whole-blood stimulations and mechanistic studies on single and purified cell populations identified distinct patterns of activation in monocytes as compared to neutrophils and invariant lymphocyte populations. Deconvoluting the role of Toll-like receptor 2/4 and Dectin-1/2 in the inflammatory response to BCG, we revealed Dectin-1/2 as dominant in neutrophils as compared to monocytes, which equally engaged both pathways. Furthermore, we quantified the role of NF-κB and NADPH/reactive oxygen species (ROS)-dependent cytokines, which triggered a JAK1/2-dependent amplification loop and accounted for 40–50% of the induced response to BCG. In sum, this study provides new insight into the molecular and cellular pathways involved in the response to BCG, establishing the basis for a new generation of immunodiagnostic tools. Frontiers Media S.A. 2017-07-13 /pmc/articles/PMC5507989/ /pubmed/28751891 http://dx.doi.org/10.3389/fimmu.2017.00796 Text en Copyright © 2017 Bisiaux, Boussier, Duffy, Quintana-Murci, Fontes and Albert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bisiaux, Aurélie
Boussier, Jeremy
Duffy, Darragh
Quintana-Murci, Lluis
Fontes, Magnus
Albert, Matthew L.
Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title_full Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title_fullStr Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title_full_unstemmed Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title_short Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity
title_sort deconvolution of the response to bacillus calmette–guérin reveals nf-κb-induced cytokines as autocrine mediators of innate immunity
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507989/
https://www.ncbi.nlm.nih.gov/pubmed/28751891
http://dx.doi.org/10.3389/fimmu.2017.00796
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