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The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse

BACKGROUND: Interleukin 15 (IL-15) is a growth and modulating factor for B, T lymphocytes and natural killer cells (NK). Its action on innate and adaptive immunity is modulated by its alpha chain receptor (IL-15Rα). The IL-15/sIL-15Rα complex (IL-15Cx) increases the bioavailability and activity of t...

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Autores principales: Moui, Antoine, Klein, Martin, Hassoun, Dorian, Dijoux, Eléonore, Cheminant, Marie-Aude, Magnan, Antoine, Bouchaud, Grégory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988344/
https://www.ncbi.nlm.nih.gov/pubmed/31996218
http://dx.doi.org/10.1186/s12931-020-1301-x
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author Moui, Antoine
Klein, Martin
Hassoun, Dorian
Dijoux, Eléonore
Cheminant, Marie-Aude
Magnan, Antoine
Bouchaud, Grégory
author_facet Moui, Antoine
Klein, Martin
Hassoun, Dorian
Dijoux, Eléonore
Cheminant, Marie-Aude
Magnan, Antoine
Bouchaud, Grégory
author_sort Moui, Antoine
collection PubMed
description BACKGROUND: Interleukin 15 (IL-15) is a growth and modulating factor for B, T lymphocytes and natural killer cells (NK). Its action on innate and adaptive immunity is modulated by its alpha chain receptor (IL-15Rα). The IL-15/sIL-15Rα complex (IL-15Cx) increases the bioavailability and activity of the cytokine in vivo. IL-15Cx has been used in diseases to dampen IL-15 inflammation by the use of soluble IL-15Ralpha specificity. Here, we aim to evaluate the interest of IL-15Cx in a mouse model of asthma. METHODS: Using a mouse model of asthma consisting in percutaneous sensitization and intranasal challenge with total house dust mite extract, we evaluated the effect of IL-15Cx injected intraperitoneally four times after a first nasal challenge. Respiratory function was assessed by the technique of forced oscillations (Flexivent®). The effect on bronchial remodeling was evaluated by lung histology. The inflammatory status was analyzed by flow cytometry. RESULTS: We observed that the IL-15Cx modulates lung and systemic inflammation by increasing NK cells, CD8(+) memory T cells and regulatory cells. However, IL-15Cx displays no effect on bronchial hyperreactivity, bronchial remodeling nor cellular bronchial infiltrate, but limits the secretion of bronchial mucus and modulates only inflammatory response in a HDM-allergic asthma murine model. CONCLUSIONS: IL-15Cx has a limited effect on immune response in asthma and has no effect on lung function in mice. Thus, it limits its therapeutic potential but might suggest a combinatory potential with other therapeutics.
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spelling pubmed-69883442020-02-03 The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse Moui, Antoine Klein, Martin Hassoun, Dorian Dijoux, Eléonore Cheminant, Marie-Aude Magnan, Antoine Bouchaud, Grégory Respir Res Research BACKGROUND: Interleukin 15 (IL-15) is a growth and modulating factor for B, T lymphocytes and natural killer cells (NK). Its action on innate and adaptive immunity is modulated by its alpha chain receptor (IL-15Rα). The IL-15/sIL-15Rα complex (IL-15Cx) increases the bioavailability and activity of the cytokine in vivo. IL-15Cx has been used in diseases to dampen IL-15 inflammation by the use of soluble IL-15Ralpha specificity. Here, we aim to evaluate the interest of IL-15Cx in a mouse model of asthma. METHODS: Using a mouse model of asthma consisting in percutaneous sensitization and intranasal challenge with total house dust mite extract, we evaluated the effect of IL-15Cx injected intraperitoneally four times after a first nasal challenge. Respiratory function was assessed by the technique of forced oscillations (Flexivent®). The effect on bronchial remodeling was evaluated by lung histology. The inflammatory status was analyzed by flow cytometry. RESULTS: We observed that the IL-15Cx modulates lung and systemic inflammation by increasing NK cells, CD8(+) memory T cells and regulatory cells. However, IL-15Cx displays no effect on bronchial hyperreactivity, bronchial remodeling nor cellular bronchial infiltrate, but limits the secretion of bronchial mucus and modulates only inflammatory response in a HDM-allergic asthma murine model. CONCLUSIONS: IL-15Cx has a limited effect on immune response in asthma and has no effect on lung function in mice. Thus, it limits its therapeutic potential but might suggest a combinatory potential with other therapeutics. BioMed Central 2020-01-29 2020 /pmc/articles/PMC6988344/ /pubmed/31996218 http://dx.doi.org/10.1186/s12931-020-1301-x Text en © The Author(s). 2020 Open Access This 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
Moui, Antoine
Klein, Martin
Hassoun, Dorian
Dijoux, Eléonore
Cheminant, Marie-Aude
Magnan, Antoine
Bouchaud, Grégory
The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title_full The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title_fullStr The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title_full_unstemmed The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title_short The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
title_sort il-15 / sil-15rα complex modulates immunity without effect on asthma features in mouse
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988344/
https://www.ncbi.nlm.nih.gov/pubmed/31996218
http://dx.doi.org/10.1186/s12931-020-1301-x
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