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dc.contributor.authorEguía, J.-
dc.contributor.authorGonzález Martínez, G.-
dc.contributor.authorDe La Peña, J.-
dc.contributor.authorGalian, J.A.-
dc.contributor.authorHernández Martínez, A.M.-
dc.contributor.authorMoya Quiles, M.R.-
dc.contributor.authorLegaz Pérez, Isabel-
dc.contributor.authorCampillo, J.A.-
dc.contributor.authorRamírez, P.-
dc.contributor.authorSánchez Bueno, F.-
dc.contributor.authorGarcía Alonso, A.M.-
dc.contributor.authorPons, J.A.-
dc.contributor.authorMinguela, A.-
dc.contributor.authorLlorente, S.-
dc.contributor.authorMuro, M.-
dc.contributor.authorBolarín, J.M.-
dc.contributor.otherFacultades, Departamentos, Servicios y Escuelas::Departamentos de la UMU::Ciencias Sociosanitarias-
dc.date.accessioned2024-07-12T08:39:30Z-
dc.date.available2024-07-12T08:39:30Z-
dc.date.issued2016-11-
dc.identifier.citationTransplantation Proceedings, 2016, Vol. 48, Issue 9, pp. 2987-2989es
dc.identifier.issnPrint: 0041-1345-
dc.identifier.issnElectronic: 1873-2623-
dc.identifier.urihttp://hdl.handle.net/10201/143026-
dc.description© 2016 Elsevier Inc. This document is the Published version of a Published Work that appeared in final form in Transplantation Proceedings. To access the final edited and published work see https://doi.org/10.1016/j.transproceed.2016.09.028-
dc.description.abstractBackground Acute rejection (AR) remains a significant cause of graft loss. Better approaches to predict AR are being investigated. Surface CD28 protein is essential for T-cell proliferation and survival as well as cytokine production. Patients and Methods Pretransplant CD4+CD28+ peripheral T cells were examined in 30 liver recipients (LRs) and 31 kidney recipients (KRs) by flow cytometry. Results Pretransplant CD4+CD28+ T cells in LRs were significantly lower in rejectors than nonrejectors (P = .002). Furthermore, the total number of CD28 molecules per cell in LRs (P = .02) as well as KRs (P = .047) was significantly lower in rejectors than nonrejectors. The healthy group did not display differences when compared with patients with end-stage liver disease or renal failure; however, stratification analysis displayed higher levels of CD4+CD28+ when compared with rejected LRs (P = .04) but not KRs. CD28 levels <41.94% were able to discriminate LRs at high risk of AR (P = .003). Similarly, a total number of CD28 molecules ≤8359 (P = .031) in LRs and ≤7669 (P = .046) in KRs correlated with high risk of AR. Conclusion The preliminary results presented herein exhibit a fast and noninvasive method that assists clinicians to prevent AR by monitoring CD4+CD28+ peripheral T cells.es
dc.formatapplication/pdfes
dc.format.extent3es
dc.languageenges
dc.publisherElsevier-
dc.relationThis work was possible thanks to support from Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Economy and Competitiveness, Grant Number PI11/02686 and PI15/01370, and cofunding of the European Union with European Fund of Regional Development (FEDER) with the principle of “A manner to build Europe.”es
dc.rightsinfo:eu-repo/semantics/embargoedAccesses
dc.titlePretransplant CD28 Biomarker (Levels of Expression and Quantification of Molecules per Cell) in Peripheral CD4+ T Cells Predicts Acute Rejection Episodes in Liver and Kidney Recipientses
dc.typeinfo:eu-repo/semantics/articlees
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0041134516306662?via%3Dihub#abs0010-
dc.embargo.termsSI-
dc.identifier.doihttps://doi.org/10.1016/j.transproceed.2016.09.028-
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