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dc.contributor.authorBoto de los Bueis, Ana
dc.contributor.authorde la Fuente, Miguel
dc.contributor.authorMontejano Milner, Rafael
dc.contributor.authordel Hierro Zarzuelo, Almudena
dc.contributor.authorVecino Cordero, Elena ORCID
dc.contributor.authorAcera Osa, Arantxa
dc.date.accessioned2023-04-28T13:02:24Z
dc.date.available2023-04-28T13:02:24Z
dc.date.issued2023-04-01
dc.identifier.citationCurrent Issues in Molecular Biology 45(4) : 2881-2894 (2023)es_ES
dc.identifier.issn1467-3045
dc.identifier.urihttp://hdl.handle.net/10810/60970
dc.description.abstractOcular diseases have a strong impact on individuals, the effects of which extend from milder visual impairment to blindness. Due to this and to their prevalence, these conditions constitute important health, social and economic challenges. Thus, improvements in their early detection and diagnosis will help dampen the impact of these conditions, both on patients and on healthcare systems alike. In this sense, identifying tear biomarkers could establish better non-invasive approaches to diagnose these diseases and to monitor responses to therapy. With this in mind, we developed a solid phase capture assay, based on antibody microarrays, to quantify S100A6, MMP-9 and CST4 in human tear samples, and we used these arrays to study tear samples from healthy controls and patients with Sjögren’s Syndrome, at times concomitant with rheumatoid arthritis. Our results point out that the detection of S100A6 in tear samples seems to be positively correlated to rheumatoid arthritis, consistent with the systemic nature of this autoinflammatory pathology. Thus, we provide evidence that antibody microarrays may potentially help diagnose certain pathologies, possibly paving the way for significant improvements in the future care of these patients.es_ES
dc.description.sponsorshipThis research was funded by the Basque Government (BIKAINTEK, grant number 48-AF-W2-2019-00006), by the University of the Basque Country (PIFIND19/02, grant number 201900016247), and by ELKARTEK (KK-2019/00086) and MINECO-Retos (PID2019-111139RB-I00) grants to E.V., as well as by FISS-21-RD21/0002/0041 to A.A.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2019-111139RB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectSjögren’s syndromees_ES
dc.subjectbiomarkeres_ES
dc.subjectS100A6es_ES
dc.subjectMMP-9es_ES
dc.subjectCST4es_ES
dc.subjectin vitro diagnosises_ES
dc.subjectantibody microarrayes_ES
dc.subjectrheumatoid arthritises_ES
dc.titleA Pilot Study of a Panel of Ocular Inflammation Biomarkers in Patients with Primary Sjögren’s Syndromees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2023-04-27T13:50:58Z
dc.rights.holder© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1467-3045/45/4/188es_ES
dc.identifier.doi10.3390/cimb45040188
dc.departamentoesBiología celular e histología
dc.departamentoeuZelulen biologia eta histologia


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© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).
Except where otherwise noted, this item's license is described as © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).