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Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity.

dc.contributor.authorGonzalez, M
dc.contributor.authorDoña, I
dc.contributor.authorPalomares, F
dc.contributor.authorCampo, P
dc.contributor.authorRodriguez, M J
dc.contributor.authorRondon, C
dc.contributor.authorGomez, F
dc.contributor.authorFernandez, T D
dc.contributor.authorPerkins, J R
dc.contributor.authorEscribese, M M
dc.contributor.authorTorres, M J
dc.contributor.authorMayorga, C
dc.contributor.funderInstitute of Health “Carlos III” of the Ministry of Economy and Competitiveness
dc.contributor.funderRETICS ARADyAL
dc.contributor.funderSara Borrell Program
dc.contributor.funderSEAIC Foundation
dc.contributor.funderAndalusian Regional Ministry of Economy and Knowledge
dc.contributor.funderAndalusian Regional Ministry of Health
dc.contributor.funderNicolas Monardes Program
dc.contributor.funderEuropean Regional Development Fund (ERDF)
dc.date.accessioned2023-01-25T09:52:28Z
dc.date.available2023-01-25T09:52:28Z
dc.date.issued2017-09-20
dc.description.abstractSubcutaneous 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.
dc.description.sponsorshipThe study was funded by grants from the Institute of Health “Carlos III” of the Ministry of Economy and Competitiveness: PI12/02481, PI15/02256 and PI15/00559, RETICS ARADyAL (RD16/0006/0001; RD16/0006/0015), Juan Rodes Program (JR15/00036) and Sara Borrell Program (CD14/00242), Salud 2000 project, SEAIC Foundation, PI-0542-2010, Andalusian Regional Ministry of Economy and Knowledge (CTS-7433), Andalusian Regional Ministry of Health, Nicolas Monardes Program (C-0044-2012 SAS2013). Grants were co-funded by the European Regional Development Fund (ERDF).
dc.description.versionSi
dc.identifier.citationGonzalez M, Doña I, Palomares F, Campo P, Rodriguez MJ, Rondon C, et al. Dermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity. Sci Rep. 2017 Sep 20;7(1):11949
dc.identifier.doi10.1038/s41598-017-12261-2
dc.identifier.essn2045-2322
dc.identifier.pmcPMC5607227
dc.identifier.pmid28931869
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607227/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41598-017-12261-2.pdf
dc.identifier.urihttp://hdl.handle.net/10668/11598
dc.issue.number1
dc.journal.titleScientific reports
dc.journal.titleabbreviationSci Rep
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.organizationHospital Universitario Regional de Málaga
dc.page.number11
dc.provenanceRealizada la curación de contenido 21/03/2025
dc.publisherNature Publishing Group
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDPI12/02481
dc.relation.projectIDPI15/02256
dc.relation.projectIDPI15/00559
dc.relation.projectIDRD16/0006/0001
dc.relation.projectIDJR15/00036
dc.relation.projectIDCD14/00242
dc.relation.projectIDPI-0542-2010
dc.relation.projectIDC-0044-2012 SAS2013
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAntigens, Dermatophagoides
dc.subjectCells, Cultured
dc.subjectCoculture Techniques
dc.subjectDermatophagoides pteronyssinus
dc.subject.decsLinfocitos T Reguladores
dc.subject.decsInterleucina-10
dc.subject.decsInmunoterapia
dc.subject.decsRinitis Alérgica
dc.subject.decsAnticuerpos Bloqueadores
dc.subject.meshAdult
dc.subject.meshAnimals
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshImmunotherapy
dc.subject.meshInjections, Subcutaneous
dc.subject.meshMale
dc.subject.meshRhinitis, Allergic
dc.subject.meshT-Lymphocytes, Regulatory
dc.subject.meshTh1 Cells
dc.subject.meshTh2 Cells
dc.subject.meshYoung Adult
dc.titleDermatophagoides pteronyssinus immunotherapy changes the T-regulatory cell activity.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number7
dspace.entity.typePublication

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