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dc.contributor.authorCalzada, David
dc.contributor.authorCremades-Jimeno, Lucía
dc.contributor.authorPedro, María Ángeles de
dc.contributor.authorBaos, Selene
dc.contributor.authorRial, Manuel
dc.contributor.authorSastre Domínguez, Joaquín 
dc.contributor.authorQuiralte, Joaquín
dc.contributor.authorFlorido, Fernando
dc.contributor.authorLahoz, Carlos
dc.contributor.authorCárdaba, Blanca
dc.contributor.otherUAM. Departamento de Medicinaes_ES
dc.contributor.otherInstituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD)es_ES
dc.date.accessioned2020-09-17T13:09:20Z
dc.date.available2020-09-17T13:09:20Z
dc.date.issued2019-11-04
dc.identifier.citationScientific Reports 9 (2019): 15942en_US
dc.identifier.issn2045-2322es_ES
dc.identifier.urihttp://hdl.handle.net/10486/691947
dc.description.abstractOlive-pollen allergy is one of the leading causes of respiratory allergy in Mediterranean countries and some areas of North America. Currently, allergen-specific immunotherapy is the only etiophatogenic treatment. However, this approach is not fully optimal, safe, or effective. Thus, efforts continue in the search for novel immunotherapy strategies, being one of the most promising the use of peptides derived from major allergens. This work tries to determine the therapeutic potential and safety of 5 dodecapeptides derived from the main allergen of olive-pollen allergy, Ole e 1. The immunomodulatory capacity of these peptides was studied using peripheral blood mononuclear cells (PBMCs) obtained from 19 olive-pollen-allergic patients and 10 healthy controls. We determined the capacity of these peptides to inhibit the proliferative response toward olive-pollen allergenic extract and to induce the regulatory cytokines, IL-10 and IL-35. To test the safety and absence of allergenicity of the peptides, the basophil activation was analyzed by flow-cytometry, using peripheral blood. The results showed that two of five peptides inhibited near to 30% the proliferative response against the total olive-pollen allergenic extract in olive-pollen-allergic patients. Inhibition increased to nearly 35% when the 5 peptides were used in combination. In both cases, a statistically significant induction of IL-10 and IL-35 secretion was observed in the supernatants of allergic patients PBMCs cultures. None of the 5 peptides induced basophil activation and cross-link inflammatory cell-bound IgE. In conclusion, these results open up new possibilities in the treatment of olive-pollen allergy, which could solve some of the problems facing current therapy approachesen_US
dc.description.sponsorshipSupported by research grants PI13/01730, PI17/01682 cofinanced by FEDER, CIBERES (ISCIII, 0013), and RETIC (RD09/0076/00101) from the Fondo de Investigación Sanitaria (Ministerio de Sanidad y Consumo, Spain). D. Calzada was supported by a contract from Comunidad de Madrid (PEJD-2016/BMD- 2682, Sistema de Garantía Juvenil), L. Cremades-Jimeno was supported by a contract from MINECO (PEJ-2014-A-31609, Sistema de Garantía Juvenil) and MA. de Pedro was supported by a contract from Comunidad de Madrid (PEJ-2017-AI/SAL-5938, Sistema de Garantía Juvenil), all cofinanced by Fondo Social Europeo (FSE) and Iniciativa de Empleo Juvenil (IEJ). S. Baos was supported by Fundación Conchita Rábago and PI17/01682.en_US
dc.format.extent12 pag.es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherNature Research (part of Springer Nature)en_US
dc.relation.ispartofScientific Reportsen_US
dc.rights© 2019 The Author(s)en_US
dc.subject.otherOlive-pollenen_US
dc.subject.otherAllergyen_US
dc.subject.otherNovel immunotherapy strategiesen_US
dc.subject.otherPeptidesen_US
dc.titleTherapeutic potential of peptides from Ole e 1 in olive-pollen allergyen_US
dc.typearticleen
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41598-019-52286-3es_ES
dc.identifier.doi10.1038/s41598-019-52286-3es_ES
dc.identifier.publicationfirstpage15942-1es_ES
dc.identifier.publicationissue9es_ES
dc.identifier.publicationlastpage15942-12es_ES
dc.relation.projectIDGobierno de España. PI13/01730es_ES
dc.relation.projectIDGobierno de España. PI17/01682es_ES
dc.relation.projectIDGobierno de España. RD09/0076/00101es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccessen
dc.authorUAMSastre Domínguez, Joaquín (267984)
dc.facultadUAMFacultad de Medicina


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