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Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4

BACKGROUND: An efficient strategy for programing dendritic cells (DCs) for cancer immunotherapy is the optimization of their maturation so that they can efficiently stimulate cancer-specific T cell responses. Interleukin (IL)-4 has appeared as an essential cytokine, widely used in vitro with granulo...

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Autores principales: Chabot, Valérie, Martin, Laurence, Meley, Daniel, Sensebé, Luc, Baron, Christophe, Lebranchu, Yvon, Dehaut, Frédéric, Velge-Roussel, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832484/
https://www.ncbi.nlm.nih.gov/pubmed/27080531
http://dx.doi.org/10.1186/s12967-016-0848-2
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author Chabot, Valérie
Martin, Laurence
Meley, Daniel
Sensebé, Luc
Baron, Christophe
Lebranchu, Yvon
Dehaut, Frédéric
Velge-Roussel, Florence
author_facet Chabot, Valérie
Martin, Laurence
Meley, Daniel
Sensebé, Luc
Baron, Christophe
Lebranchu, Yvon
Dehaut, Frédéric
Velge-Roussel, Florence
author_sort Chabot, Valérie
collection PubMed
description BACKGROUND: An efficient strategy for programing dendritic cells (DCs) for cancer immunotherapy is the optimization of their maturation so that they can efficiently stimulate cancer-specific T cell responses. Interleukin (IL)-4 has appeared as an essential cytokine, widely used in vitro with granulocyte macrophage-colony stimulating factor (GM-CSF) to differentiate monocytes into immature DCs (iDC) and to prevent macrophage formation. Conflicting data have been published regarding the effect of IL-4 on functional DC maturation. To further understand IL-4’s effects on DC maturation and function in vitro, we choose the most commonly used maturation factor tumor necrosis factor (TNF)-α. METHODS: Human monocyte-derived iDC were treated for 48 h with GM-CSF and TNF-α in the presence (IL-4(+)-DC) or absence (IL-4(−)-DC) of IL-4 and functions of both DC populations were compared. RESULTS: On mixed lymphocyte reaction assay, IL-4(+)-DC were less potent than IL-4(−)-DC at inducing the proliferation of allogeneic CD4(+) T cells and the proportion of activated T cells expressing CD69 and/or CD25 was smaller. Interleukin-4 reduced the cell-surface expression of TNF-α-induced DC maturation markers CD83, CD86, HLA-DR and CD25 and generated a heterogeneous population of DCs. IL-4(+)-DC secreted less IL-12 and more IL-10 than IL-4(−)-DC following activation by soluble CD40L, and IL-4(+)-DC-activated T cells secreted lesser amounts of T helper (Th) 1 cytokines (IL-2 and interferon-γ). Importantly, IL-4 impaired the in vitro migratory capacity of DCs in response to CCL21 and CCL19 chemokines. This effect was related to reduced expression of CCR7 at both mRNA and protein levels. CONCLUSION: Interleukin-4 used with GM-CSF and TNF-α during the maturation of DCs in vitro impaired DC functions and disturbed the maturation effect of TNF-α. Finally, our study reinforces the view that the quality of the DC maturation stimulus, which regulates DC migration and cytokine production, may be a decisive feature of the immunogenicity of DCs.
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spelling pubmed-48324842016-04-16 Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4 Chabot, Valérie Martin, Laurence Meley, Daniel Sensebé, Luc Baron, Christophe Lebranchu, Yvon Dehaut, Frédéric Velge-Roussel, Florence J Transl Med Research BACKGROUND: An efficient strategy for programing dendritic cells (DCs) for cancer immunotherapy is the optimization of their maturation so that they can efficiently stimulate cancer-specific T cell responses. Interleukin (IL)-4 has appeared as an essential cytokine, widely used in vitro with granulocyte macrophage-colony stimulating factor (GM-CSF) to differentiate monocytes into immature DCs (iDC) and to prevent macrophage formation. Conflicting data have been published regarding the effect of IL-4 on functional DC maturation. To further understand IL-4’s effects on DC maturation and function in vitro, we choose the most commonly used maturation factor tumor necrosis factor (TNF)-α. METHODS: Human monocyte-derived iDC were treated for 48 h with GM-CSF and TNF-α in the presence (IL-4(+)-DC) or absence (IL-4(−)-DC) of IL-4 and functions of both DC populations were compared. RESULTS: On mixed lymphocyte reaction assay, IL-4(+)-DC were less potent than IL-4(−)-DC at inducing the proliferation of allogeneic CD4(+) T cells and the proportion of activated T cells expressing CD69 and/or CD25 was smaller. Interleukin-4 reduced the cell-surface expression of TNF-α-induced DC maturation markers CD83, CD86, HLA-DR and CD25 and generated a heterogeneous population of DCs. IL-4(+)-DC secreted less IL-12 and more IL-10 than IL-4(−)-DC following activation by soluble CD40L, and IL-4(+)-DC-activated T cells secreted lesser amounts of T helper (Th) 1 cytokines (IL-2 and interferon-γ). Importantly, IL-4 impaired the in vitro migratory capacity of DCs in response to CCL21 and CCL19 chemokines. This effect was related to reduced expression of CCR7 at both mRNA and protein levels. CONCLUSION: Interleukin-4 used with GM-CSF and TNF-α during the maturation of DCs in vitro impaired DC functions and disturbed the maturation effect of TNF-α. Finally, our study reinforces the view that the quality of the DC maturation stimulus, which regulates DC migration and cytokine production, may be a decisive feature of the immunogenicity of DCs. BioMed Central 2016-04-14 /pmc/articles/PMC4832484/ /pubmed/27080531 http://dx.doi.org/10.1186/s12967-016-0848-2 Text en © Chabot et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chabot, Valérie
Martin, Laurence
Meley, Daniel
Sensebé, Luc
Baron, Christophe
Lebranchu, Yvon
Dehaut, Frédéric
Velge-Roussel, Florence
Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title_full Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title_fullStr Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title_full_unstemmed Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title_short Unexpected impairment of TNF-α-induced maturation of human dendritic cells in vitro by IL-4
title_sort unexpected impairment of tnf-α-induced maturation of human dendritic cells in vitro by il-4
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832484/
https://www.ncbi.nlm.nih.gov/pubmed/27080531
http://dx.doi.org/10.1186/s12967-016-0848-2
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