Systemic regulatory T cells and IL-6 as prognostic factors for anatomical improvement of uveitic macular edema
dc.contributor.author | Matas, Jessica | |
dc.contributor.author | Díaz Valle, David | |
dc.contributor.author | Molins, Blanca | |
dc.date.accessioned | 2024-12-03T09:04:12Z | |
dc.date.available | 2024-12-03T09:04:12Z | |
dc.date.issued | 2020-09-15 | |
dc.description.abstract | Purpose: To investigate whether systemic immune mediators and circulating regulatory T cells (Tregs) could be prognostic factors for anatomic outcomes in macular edema secondary to non-infectious uveitis (UME). Methods: Multicenter, prospective, observational, 12-month follow-up study of 60 patients with UME. Macular edema was defined as central subfield thickness (CST) > 300 μm measured with spectral domain optical coherence tomography (SD-OCT). Serum samples and peripheral blood mononuclear cells (PBMC) were obtained from venous blood extraction at baseline. Serum levels of IL-1β, IL-6, IL-8, IL-17, MCP-1, TNF-α, IL-10, and VEGF were determined by Luminex. Tregs population, defined as CD3+CD4+FoxP3+ in PBMC, was determined by flow cytometry. Main outcome measure was the predictive association between searched mediators and CST sustained improvement, defined as CST < 300 microns or a 20% CST decrease, at 6 months maintained until 12-months compared to baseline levels. Results: Multivariate logistic regression analysis showed an association between CST sustained improvement at 12 months follow-up and IL-6 and Tregs baseline levels. Higher IL-6 levels were associated with less events of UME improvement (OR: 0.67, 95% CI (0.45–1.00), P = 0.042), whereas higher levels of Tregs favored such improvement (OR: 1.25, 95% CI: 1.12–2.56, P = 0.049). Conclusions: Increased levels of Tregs and reduced levels of IL-6 in serum may be prognostic factors of sustained anatomical improvement in UME. These findings could enforce the opportunity to develop more efficient and personalized therapeutic approaches to improve long-term visual prognosis in patients with UME. | |
dc.description.department | Depto. de Inmunología, Oftalmología y ORL | |
dc.description.faculty | Fac. de Medicina | |
dc.description.refereed | TRUE | |
dc.description.sponsorship | Instituto de Salud Carlos III | |
dc.description.sponsorship | Ministerio de Ciencia e Innovación (España) | |
dc.description.sponsorship | Unión Europea | |
dc.description.status | pub | |
dc.identifier.citation | Matas J, Llorenç V, Fonollosa A, Díaz-Valle D, Esquinas C, de la Maza MTS, Figueras-Roca M, Artaraz J, Berasategui B, Mesquida M, Adán A and Molins B (2020) Systemic Regulatory T Cells and IL-6 as Prognostic Factors for Anatomical Improvement of Uveitic Macular Edema. Front. Immunol. 11:579005. doi: 10.3389/fimmu.2020.579005 | |
dc.identifier.doi | 10.3389/fimmu.2020.579005 | |
dc.identifier.essn | 1664-3224 | |
dc.identifier.officialurl | https://doi.org/10.3389/fimmu.2020.579005 | |
dc.identifier.relatedurl | https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2020.579005/full | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/111929 | |
dc.journal.title | Frontiers in Immunology | |
dc.language.iso | eng | |
dc.page.initial | 579005 | |
dc.publisher | Frontiers Media | |
dc.relation.projectID | PI13/00217 | |
dc.relation.projectID | PI13/00217 | |
dc.relation.projectID | RD16/0008 | |
dc.rights | Attribution 4.0 International | en |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject.cdu | 612.017 | |
dc.subject.keyword | macular edema | |
dc.subject.keyword | uveitis | |
dc.subject.keyword | cytokines | |
dc.subject.keyword | regulatory T cells | |
dc.subject.keyword | biomarkers | |
dc.subject.ucm | Ciencias Biomédicas | |
dc.subject.unesco | 32 Ciencias Médicas | |
dc.title | Systemic regulatory T cells and IL-6 as prognostic factors for anatomical improvement of uveitic macular edema | |
dc.type | journal article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 11 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 3e2b98e5-5c02-400b-8823-90887624c010 | |
relation.isAuthorOfPublication.latestForDiscovery | 3e2b98e5-5c02-400b-8823-90887624c010 |
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