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dc.contributor.authorUgalde-Triviño, Lola
dc.contributor.authorMolina-Jiménez, Francisca
dc.contributor.authorH-Vázquez, Juan
dc.contributor.authorRelaño-Rupérez, Carlos
dc.contributor.authorArias-González, Laura
dc.contributor.authorCasabona, Sergio
dc.contributor.authorPérez-Fernández, María Teresa
dc.contributor.authorMartín-Domínguez, Verónica
dc.contributor.authorFernández-Pacheco, Jennifer
dc.contributor.authorLucendo, Alfredo J
dc.contributor.authorBernardo, David
dc.contributor.authorSantander, Cecilio
dc.contributor.authorMajano, Pedro
dc.date.accessioned2024-07-02T12:10:40Z
dc.date.available2024-07-02T12:10:40Z
dc.date.issued2024
dc.identifier.citationFront Immunol. 2024 Apr 5:15:1374611.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/19907
dc.description.abstractOBJECTIVES The aim of the study was to characterize the circulating immunome of patients with EoE before and after proton pump inhibitor (PPI) treatment in order to identify potential non-invasive biomarkers of treatment response. METHODS PBMCs from 19 healthy controls and 24 EoE patients were studied using a 39-plex spectral cytometry panel. The plasmacytoid dendritic cell (pDC) population was differentially characterized by spectral cytometry analysis and immunofluorescence assays in esophageal biopsies from 7 healthy controls and 13 EoE patients. RESULTS Interestingly, EoE patients at baseline had lower levels of circulating pDC compared with controls. Before treatment, patients with EoE who responded to PPI therapy had higher levels of circulating pDC and classical monocytes, compared with non-responders. Moreover, following PPI therapy pDC levels were increased in all EoE patients, while normal levels were only restored in PPI-responding patients. Finally, circulating pDC levels inversely correlated with peak eosinophil count and pDC count in esophageal biopsies. The number of tissue pDCs significantly increased during active EoE, being even higher in non-responder patients when compared to responder patients pre-PPI. pDC levels decreased after PPI intake, being further restored almost to control levels in responder patients post-PPI. CONCLUSIONS We hereby describe a unique immune fingerprint of EoE patients at diagnosis. Moreover, circulating pDC may be also used as a novel non-invasive biomarker to predict subsequent response to PPI treatment.es_ES
dc.description.sponsorshipThe author(s) declare financial support was received for the research, authorship, and/or publication of this article. PM and CS are supported by grants PI17/0008 and ISCIII-Proteored 2019 of Instituto de Salud Carlos III (ISCIII, Spain) and co-funded by Fondo Europeo de Desarrollo Regional (FEDER). CS is also funded by Asociación Española de Gastroenterologıa (AEG) 2019 ́ grant. DB is funded through the Spanish Ministry of Science [PID2019-104218RB-I00], Programa Estratégico Instituto de Biologıa y Gene ́ ́tica Molecular (IBGM Junta de Castilla y León. Ref. CCVC8485) and the European Commission – NextGenerationEU (Regulation EU 2020/2094), through CSIC’s Global Health Platform. LU-T is recipient of an INVESTIGO contract from Comunidad de Madrid (09-PIN1-00015.6/2022) partly funded by the European Social Fund, NextGenerationEU, and Recovery, Transformation and Resilience Plan. CR-R is recipient of an INVESTIGO contract from Ministry of Labor and Social Economy, the national public employment service (SEPE) (INVESTIGO Exp. 2022‐C23.I01.P03. S0020‐0000031) partly funded by the European Social Fund, NextGenerationEU, and Recovery, Transformation and Resilience Plan.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Media es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshProton Pump Inhibitors es_ES
dc.subject.meshEosinophilic Esophagitis es_ES
dc.subject.meshBiomarkers es_ES
dc.subject.meshDendritic Cells es_ES
dc.subject.meshHumans es_ES
dc.subject.meshMale es_ES
dc.subject.meshFemale es_ES
dc.subject.meshAdult es_ES
dc.subject.meshMiddle Aged es_ES
dc.subject.meshEosinophils es_ES
dc.subject.meshTreatment Outcome es_ES
dc.subject.meshYoung Adult es_ES
dc.subject.meshBiopsy es_ES
dc.subject.meshCase-Control Studies es_ES
dc.titleCirculating immunome fingerprint in eosinophilic esophagitis is associated with clinical response to proton pump inhibitor treatment.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID38646544es_ES
dc.format.volume15es_ES
dc.format.page1374611es_ES
dc.identifier.doi10.3389/fimmu.2024.1374611es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) es_ES
dc.contributor.funderMinisterio de Ciencia (España) es_ES
dc.contributor.funderUnión Europea. Comisión Europea. NextGenerationEU es_ES
dc.contributor.funderComunidad de Madrid (España) es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1664-3224es_ES
dc.relation.publisherversion10.3389/fimmu.2024.1374611es_ES
dc.identifier.journalFrontiers in immunologyes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Señalización Intercelular durante el Desarrollo y la Enfermedad Cardiovasculares_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PI17/0008es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2019-104218RB-I00es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/CCVC8485es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/09-PIN1-00015.6/2022es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/2022‐C23.I01.P03es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/S0020‐0000031es_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 Internacional