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Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity

Subcutaneous specific immunotherapy (SCIT) has been shown to modify the Dermatophagoides pteronissinus (DP) allergic response, characterized by generation of Treg cells. However, studies have reported no changes in the proportion of Treg cells after immunotherapy, indicating that the effects may be...

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Autores principales: Gonzalez, M., Doña, I., Palomares, F., Campo, P., Rodriguez, M. J., Rondon, C., Gomez, F., Fernandez, T. D., Perkins, J. R., Escribese, M. M., Torres, M. J., Mayorga, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607227/
https://www.ncbi.nlm.nih.gov/pubmed/28931869
http://dx.doi.org/10.1038/s41598-017-12261-2
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author Gonzalez, M.
Doña, I.
Palomares, F.
Campo, P.
Rodriguez, M. J.
Rondon, C.
Gomez, F.
Fernandez, T. D.
Perkins, J. R.
Escribese, M. M.
Torres, M. J.
Mayorga, C.
author_facet Gonzalez, M.
Doña, I.
Palomares, F.
Campo, P.
Rodriguez, M. J.
Rondon, C.
Gomez, F.
Fernandez, T. D.
Perkins, J. R.
Escribese, M. M.
Torres, M. J.
Mayorga, C.
author_sort Gonzalez, M.
collection PubMed
description Subcutaneous specific immunotherapy (SCIT) has been shown to modify the Dermatophagoides pteronissinus (DP) allergic response, characterized by generation of Treg cells. However, studies have reported no changes in the proportion of Treg cells after immunotherapy, indicating that the effects may be due to modifications in their regulatory activities. We aimed to determine whether Tregs generated by DP-SCIT can switch the allergic response to tolerant and study the involvement of suppressive cytokines on it. Twenty-four DP-allergic rhinitis patients were recruited, 16 treated with DP-SCIT and 8 untreated. Treg and T effector cells were isolated before and after DP-SCIT, and cocultured in different combinations with α-IL-10, α-TGF-β blocking antibodies and nDer p 1. Treg cells after DP-SCIT increased Th1 and decreased Th2 and Th9 proliferation. Similarly, they increased IL-10 and decreased IL-4 and IL-9-producing cells. α-IL-10 affected the activity of Treg cells obtained after DP-SCIT only. Finally, DP-specific IgG4 levels, Treg percentage and IL-10 production were correlated after DP-SCIT. These results demonstrate that DP-SCIT induces Treg cells with different suppressive activities. These changes could be mediated by IL-10 production and appear to play an important role in the induction of the tolerance response leading to a clinical improvement of symptoms.
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spelling pubmed-56072272017-09-24 Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity Gonzalez, M. Doña, I. Palomares, F. Campo, P. Rodriguez, M. J. Rondon, C. Gomez, F. Fernandez, T. D. Perkins, J. R. Escribese, M. M. Torres, M. J. Mayorga, C. Sci Rep Article Subcutaneous specific immunotherapy (SCIT) has been shown to modify the Dermatophagoides pteronissinus (DP) allergic response, characterized by generation of Treg cells. However, studies have reported no changes in the proportion of Treg cells after immunotherapy, indicating that the effects may be due to modifications in their regulatory activities. We aimed to determine whether Tregs generated by DP-SCIT can switch the allergic response to tolerant and study the involvement of suppressive cytokines on it. Twenty-four DP-allergic rhinitis patients were recruited, 16 treated with DP-SCIT and 8 untreated. Treg and T effector cells were isolated before and after DP-SCIT, and cocultured in different combinations with α-IL-10, α-TGF-β blocking antibodies and nDer p 1. Treg cells after DP-SCIT increased Th1 and decreased Th2 and Th9 proliferation. Similarly, they increased IL-10 and decreased IL-4 and IL-9-producing cells. α-IL-10 affected the activity of Treg cells obtained after DP-SCIT only. Finally, DP-specific IgG4 levels, Treg percentage and IL-10 production were correlated after DP-SCIT. These results demonstrate that DP-SCIT induces Treg cells with different suppressive activities. These changes could be mediated by IL-10 production and appear to play an important role in the induction of the tolerance response leading to a clinical improvement of symptoms. Nature Publishing Group UK 2017-09-20 /pmc/articles/PMC5607227/ /pubmed/28931869 http://dx.doi.org/10.1038/s41598-017-12261-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gonzalez, M.
Doña, I.
Palomares, F.
Campo, P.
Rodriguez, M. J.
Rondon, C.
Gomez, F.
Fernandez, T. D.
Perkins, J. R.
Escribese, M. M.
Torres, M. J.
Mayorga, C.
Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title_full Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title_fullStr Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title_full_unstemmed Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title_short Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity
title_sort dermatophagoides pteronyssinus immunotherapy changes the t-regulatory cell activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607227/
https://www.ncbi.nlm.nih.gov/pubmed/28931869
http://dx.doi.org/10.1038/s41598-017-12261-2
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