dc.creatorMoore, C.
dc.creatorSauma Mahaluf, Daniela
dc.creatorReyes, P. A.
dc.creatorMorales, J.
dc.creatorRosemblatt Silber, Mario César
dc.creatorBono Merino, María Rosa
dc.creatorFierro, J. A.
dc.date.accessioned2019-03-11T12:59:12Z
dc.date.available2019-03-11T12:59:12Z
dc.date.created2019-03-11T12:59:12Z
dc.date.issued2010
dc.identifierTransplantation Proceedings, Volumen 42, Issue 1, 2018, Pages 371-375
dc.identifier00411345
dc.identifier10.1016/j.transproceed.2009.12.044
dc.identifierhttps://repositorio.uchile.cl/handle/2250/164949
dc.description.abstractBackground: CD4+CD25+Foxp3+ regulatory T cells (Treg) play an essential role in immune tolerance, suppressing responses against self-antigens. Additionally, Treg play an important role in maintaining immunosuppression to alloantigens as well as to other antigens. It is well known that in the gut, a subset of dendritic cells produces retinoic acid (RA), which together with transforming growth factor (TGF-β) is able to differentiate naïve T cells into Treg. The aim of this study was to establish the role of antigen-presenting cells (APC) in the differentiation of allogeneic Tregs under the effect of RA and TGF-β. Methods: Splenic CD4+CD25- naïve T cells from C57BL/6 mice were co-cultured with splenic CD11c-enriched APC from Balb/c mice in the presence of TGF-β, RA, and interleukin (IL-2). After 6 days of culture, cells were analyzed for the expression of Foxp3 by flow cytometry. Additionally, we investigated the role of B cells and dendritic cells (DCs) and their stimulatory capacity in
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceTransplantation Proceedings
dc.subjectSurgery
dc.subjectTransplantation
dc.titleDendritic Cells and B Cells Cooperate in the Generation of CD4+CD25+FOXP3+ Allogeneic T Cells
dc.typeArtículo de revista


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