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Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation

Unresolved inflammation is a common feature in the pathogenesis of chronic inflammatory/autoimmune diseases. The factors produced by macrophages eliminating apoptotic cells during resolution are crucial to terminate inflammation, and for subsequent tissue healing. We demonstrated here that the facto...

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Autores principales: Bonnefoy, Francis, Gauthier, Thierry, Vallion, Romain, Martin-Rodriguez, Omayra, Missey, Anais, Daoui, Anna, Valmary-Degano, Séverine, Saas, Philippe, Couturier, Mélanie, Perruche, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277856/
https://www.ncbi.nlm.nih.gov/pubmed/30542342
http://dx.doi.org/10.3389/fimmu.2018.02586
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author Bonnefoy, Francis
Gauthier, Thierry
Vallion, Romain
Martin-Rodriguez, Omayra
Missey, Anais
Daoui, Anna
Valmary-Degano, Séverine
Saas, Philippe
Couturier, Mélanie
Perruche, Sylvain
author_facet Bonnefoy, Francis
Gauthier, Thierry
Vallion, Romain
Martin-Rodriguez, Omayra
Missey, Anais
Daoui, Anna
Valmary-Degano, Séverine
Saas, Philippe
Couturier, Mélanie
Perruche, Sylvain
author_sort Bonnefoy, Francis
collection PubMed
description Unresolved inflammation is a common feature in the pathogenesis of chronic inflammatory/autoimmune diseases. The factors produced by macrophages eliminating apoptotic cells during resolution are crucial to terminate inflammation, and for subsequent tissue healing. We demonstrated here that the factors produced by macrophages eliminating apoptotic cells were sufficient to reboot the resolution of inflammation in vivo, and thus definitively terminated ongoing chronic inflammation. These factors were called SuperMApo and revealed pro-resolutive properties and accelerated acute inflammation resolution, as attested by both increased phagocytic capacities of macrophages and enhanced thioglycollate-induced peritonitis resolution. Activated antigen-presenting cells exposed to SuperMApo accelerated their return to homeostasis and demonstrated pro-regulatory T cell properties. In mice with ongoing collagen-induced arthritis, SuperMApo injection resolved and definitively terminated chronic inflammation. The same pro-resolving properties were observed in human settings in addition to xenogeneic colitis and graft-vs.-host disease modulation, highlighting SuperMApo as a new therapeutic opportunity to circumvent inflammatory diseases.
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spelling pubmed-62778562018-12-12 Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation Bonnefoy, Francis Gauthier, Thierry Vallion, Romain Martin-Rodriguez, Omayra Missey, Anais Daoui, Anna Valmary-Degano, Séverine Saas, Philippe Couturier, Mélanie Perruche, Sylvain Front Immunol Immunology Unresolved inflammation is a common feature in the pathogenesis of chronic inflammatory/autoimmune diseases. The factors produced by macrophages eliminating apoptotic cells during resolution are crucial to terminate inflammation, and for subsequent tissue healing. We demonstrated here that the factors produced by macrophages eliminating apoptotic cells were sufficient to reboot the resolution of inflammation in vivo, and thus definitively terminated ongoing chronic inflammation. These factors were called SuperMApo and revealed pro-resolutive properties and accelerated acute inflammation resolution, as attested by both increased phagocytic capacities of macrophages and enhanced thioglycollate-induced peritonitis resolution. Activated antigen-presenting cells exposed to SuperMApo accelerated their return to homeostasis and demonstrated pro-regulatory T cell properties. In mice with ongoing collagen-induced arthritis, SuperMApo injection resolved and definitively terminated chronic inflammation. The same pro-resolving properties were observed in human settings in addition to xenogeneic colitis and graft-vs.-host disease modulation, highlighting SuperMApo as a new therapeutic opportunity to circumvent inflammatory diseases. Frontiers Media S.A. 2018-11-13 /pmc/articles/PMC6277856/ /pubmed/30542342 http://dx.doi.org/10.3389/fimmu.2018.02586 Text en Copyright © 2018 Bonnefoy, Gauthier, Vallion, Martin-Rodriguez, Missey, Daoui, Valmary-Degano, Saas, Couturier and Perruche. 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) and the copyright owner(s) 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
Bonnefoy, Francis
Gauthier, Thierry
Vallion, Romain
Martin-Rodriguez, Omayra
Missey, Anais
Daoui, Anna
Valmary-Degano, Séverine
Saas, Philippe
Couturier, Mélanie
Perruche, Sylvain
Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title_full Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title_fullStr Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title_full_unstemmed Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title_short Factors Produced by Macrophages Eliminating Apoptotic Cells Demonstrate Pro-Resolutive Properties and Terminate Ongoing Inflammation
title_sort factors produced by macrophages eliminating apoptotic cells demonstrate pro-resolutive properties and terminate ongoing inflammation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277856/
https://www.ncbi.nlm.nih.gov/pubmed/30542342
http://dx.doi.org/10.3389/fimmu.2018.02586
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