Gram-negative enterobacteria induce tolerogenic maturation in dexamethasone conditioned dendritic cells

dc.contributor.authorCabezón Cabello, Raquel
dc.contributor.authorRicart, Elena
dc.contributor.authorEspaña, Carolina
dc.contributor.authorPanés Díaz, Julià
dc.contributor.authorBenítez-Ribas, Daniel
dc.date.accessioned2018-09-18T14:25:31Z
dc.date.available2018-09-18T14:25:31Z
dc.date.issued2012-12-27
dc.date.updated2018-09-18T14:25:32Z
dc.description.abstractDendritic cells have been investigated in clinical trials, predominantly with the aim of stimulating immune responses against tumours or infectious diseases. Thus far, however, no clinical studies have taken advantage of their specific immunosuppressive potential. Tolerogenic DCs may represent a new therapeutic strategy for human immune-based diseases, such as Crohn's disease, where the perturbations of the finely tuned balance between the immune system and the microflora result in disease. In the present report, we describe the generation of tolerogenic DCs from healthy donors and Crohn's disease patients using clinical-grade reagents in combination with dexamethasone as immunosuppressive agent and characterize their response to maturation stimuli. Interestingly, we found out that dexamethasone-conditioned DCs keep their tolerogenic properties to Gram-negative bacteria. Other findings included in this study demonstrate that the combination of dexamethasone with a specific cytokine cocktail yielded clinical-grade DCs with the following characteristics: a semi-mature phenotype, a pronounced shift towards anti-inflammatory versus inflammatory cytokine production and low T-cell stimulatory properties. Importantly, in regard to their clinical application, the tolerogenic phenotype of DCs remained stable after the elimination of dexamethasone and after a second stimulation with LPS or bacteria. All these properties make this cell product suitable to be tested in clinical trials of inflammatory conditions including Crohn's disease.
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec639460
dc.identifier.issn1932-6203
dc.identifier.pmid23300676
dc.identifier.urihttps://hdl.handle.net/2445/124662
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0052456
dc.relation.ispartofPLoS One, 2012, vol. 7, num. 12, p. e52456
dc.relation.urihttps://doi.org/10.1371/journal.pone.0052456
dc.rightscc-by (c) Cabezón Cabello, Raquel et al., 2012
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationCèl·lules dendrítiques
dc.subject.classificationMalaltia de Crohn
dc.subject.classificationImmunologia
dc.subject.otherDendritic cells
dc.subject.otherCrohn's disease
dc.subject.otherImmunology
dc.titleGram-negative enterobacteria induce tolerogenic maturation in dexamethasone conditioned dendritic cells
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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