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Monitoring of B Cell in Kidney Transplantation: Development of a Novel Clusters Analysis and Role of Transitional B Cells in Transplant Outcome

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dc.contributor.author Alfaro, Rafael
dc.contributor.author Legaz, Isabel
dc.contributor.author González-Martínez, Gema
dc.contributor.author Jiménez-Coll, Víctor
dc.contributor.author Martínez-Banaclocha, Helios
dc.contributor.author Antonio-Galian, José
dc.contributor.author Botella, Carmen
dc.contributor.author de-la-Peña-Moral, Jesús
dc.contributor.author Rosa-Moya-Quiles, María
dc.contributor.author Antonio-Campillo, José
dc.contributor.author Minguela-Puras, Alfredo
dc.contributor.author Llorente Vinas, Santiago
dc.contributor.author Muro-Pérez, Manuel
dc.date.accessioned 2025-11-24T15:11:52Z
dc.date.available 2025-11-24T15:11:52Z
dc.date.issued 2021-04
dc.identifier.citation Alfaro R, Legaz I, González-Martínez G, Jimenez-Coll V, Martínez-Banaclocha H, Galián JA, et al. Monitoring of B Cell in Kidney Transplantation: Development of a Novel Clusters Analysis and Role of Transitional B Cells in Transplant Outcome. Diagnostics. 1 de abril de 2021;11(4):641.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/22314
dc.description.abstract BACKGROUND: B lymphocytes (BL) seem to play an important role in transplantation, although the and role of different subpopulations in monitoring and outcome is not clear. Our aim was to monitoring immunological profiles based on BL subpopulations in kidney recipients (KR) with the risk of acute rejection (AR). METHODS: Monitoring of BL subpopulations was performed by flow cytometry in PBLs before transplantation and three and six months after transplantation (PTX). We used two methodological approaches, a traditional analysis, and a novel cluster analysis, to determine the association between BL subpopulations, AR incidence, and graft function. RESULTS: After three months of PTX, KRs with a B phenotype enriched in transitional BL and plasmablasts had better kidney function and lower AR incidence. KRs with decreased transitional BL and plasmablasts were associated with lower kidney function and higher AR PTX. KRs that had an increase in transitional BL PTX had a better clinical outcome. The increase in transitory BL during PTX was also associated with an increase in Tregs. Indeed, KRs receiving thymoglobulin as induction therapy showed a slight decrease in the relative frequency of naive BLs after three months of PTX. CONCLUSION: The monitoring of BL subpopulations may serve as a non-invasive tool to improve immunological follow-up of patients after kidney transplantation. However, further studies are needed to confirm the obtained results, define cut-off values, and standardize more optimal and even custom/customized protocols.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional 
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/es/  *
dc.title Monitoring of B Cell in Kidney Transplantation: Development of a Novel Clusters Analysis and Role of Transitional B Cells in Transplant Outcome
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 33916199
dc.relation.publisherversion https://www.mdpi.com/2075-4418/11/4/641
dc.identifier.doi 10.3390/diagnostics11040641
dc.journal.title Diagnostics
dc.identifier.essn 2075-4418


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