Toll-like receptors as diagnostic targets in pellucid marginal degeneration

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Cirurxía e Especialidades Médico-Cirúrxicas
dc.contributor.authorRegueiro, Uxía 
dc.contributor.authorPérez Mato, María
dc.contributor.authorHervella, Pablo
dc.contributor.authorCampos, Francisco
dc.contributor.authorSobrino, Tomás
dc.contributor.authorLema Gesto, María Isabel
dc.date.accessioned2026-02-03T07:50:22Z
dc.date.available2026-02-03T07:50:22Z
dc.date.issued2020-09-02
dc.description.abstractThe main purpose of this study is to evaluate the diagnostic role of Toll-like receptors 2 (TLR2) and 4 (TLR4) expression in corneal and conjunctival epithelial cells of eyes with pellucid marginal degeneration (PMD) compared to keratoconus patients (KC) and control subjects. A prospective case-control study in 29 PMD eyes, 109 KC eyes and 72 healthy eyes was done. All participants were subjected to a clinical, topographic, aberrometric and tomographic exam with extraction of corneal and conjunctival epithelial cells through scraping. The TLR2 and TLR4 expression was measured with flow cytometry. Receiver operating characteristic (ROC) curve analysis was used to determine the most appropriate cutoff point for predicting the risk of PMD and KC. Correlations between TLR2/TLR4 expression and the severity of PMD/KC were evaluated. A TLRs follow-up review was made 19 ± 4 months after to the first review. As result, mean expression of TLR2 and TLR4 in both corneal and conjunctival epithelial cells was significantly higher in eyes with corneal ectasia (PMD and KC) than in control eyes (all p < 0.05). Conjunctival TLR4 expression showed the highest capacity to diagnose the existence of PMD (odd ratio 42.84; 95% confidence interval:6.20–296.20; p < 0.0001) after adjusting by eye rubbing and steeper corneal meridian. Moreover, we found an association between the TLR2/TLR4 overexpression with the severity of the PMD and KC measured by corneal topographic, aberrometric and tomographic quantitative parameters (all p < 0.05). Differences on TLR2/TLR4 expression between study groups were maintained during the follow-up period. In conclusion, the TLR2/TLR4 overexpression in corneal and conjunctival epithelial cells of PMD and KC patients compared to healthy control subjects have demonstrated their role as diagnostic target in both corneal ectatic disorders.
dc.description.peerreviewedSI
dc.description.sponsorshipThis project has been awarded grants from the Spanish Ministry of Economy and Competitiveness(Instituto de Salud Carlos III: PI14/00247); Xunta de Galicia (Consellería de Educación: GRC 2014/027 and IN607A2018/3), and the European Union program ERFD. T. Sobrino (CPII17/00027) and F. Campos (CPII19/00020) recipients of a research contract from the Miguel Servet Program (National Institute of Health Carlos III). Similarly, U. Regueiro was awarded a predoctoral Fellowship from the Xunta de Galicia (ED481A-2015/001). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
dc.identifier.citationhttps://doi.org/10.1016/j.exer.2020.108211
dc.identifier.doi10.1016/j.exer.2020.108211
dc.identifier.essn1096-0007
dc.identifier.urihttps://hdl.handle.net/10347/45633
dc.journal.titleExperimental Eye Research
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/PI14%2F00247/ES/Bloqueo de la inmunidad innata en la prevención de la progresión del Queratocono
dc.relation.publisherversionhttps://doi.org/10.1016/j.exer.2020.108211
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCorneal ectasia
dc.subjectInnate immunity
dc.subjectKeratoconus
dc.subjectPellucid marginal degeneration
dc.subjectToll-like receptors 2
dc.subjectToll-like receptors 4
dc.titleToll-like receptors as diagnostic targets in pellucid marginal degeneration
dc.typejournal article
dc.type.hasVersionAM
dc.volume.number200
dspace.entity.typePublication
relation.isAuthorOfPublication79b322b7-4192-4335-aed0-4f9864bec97e
relation.isAuthorOfPublication79b322b7-4192-4335-aed0-4f9864bec97e
relation.isAuthorOfPublicatione01c5f69-49e1-4b68-8c32-96eb39718d39
relation.isAuthorOfPublication.latestForDiscovery79b322b7-4192-4335-aed0-4f9864bec97e

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