Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/93453
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dc.contributor.authorPozo Rubio, Tamara-
dc.contributor.authorMarcos, Ascensión-
dc.contributor.authorKoning, F.-
dc.contributor.authorMujico, Jorge R.-
dc.contributor.authorSanz Herranz, Yolanda-
dc.contributor.authorNova, Esther-
dc.date.accessioned2014-03-12T08:38:39Z-
dc.date.available2014-03-12T08:38:39Z-
dc.date.issued2013-
dc.identifier.citationProceedings of the Nutrition Society 72 (2013)es_ES
dc.identifier.issn0029-6651-
dc.identifier.urihttp://hdl.handle.net/10261/93453-
dc.descriptionPresentado en el 6th Internationa Workshop on immunonutrition 15th-17th October 2012 Palma de Mallorcaes_ES
dc.description.abstractGluten peptides have been shown to induce cytotoxicity and IL-15 production even in in vitro studies with cell lines and biopsies of healthy subjects(1,2). We hypothesized that the inflammatory milieu caused by gluten antigens might be counteracted by certain species or strains of the commensal intestinal microbiota in interaction with the immune system. The aim of the present study was to evaluate the effect of different bacterialstrains from breastfed (BF) and formula-fed (FF) infants at risk ofceliac disease on cytokine production and T cell proliferationin vitro. Two combinations of predominant bacteria from fecal samples ofBF (Escheriquia coli (51.6%), Lactobacillus casei (19.4%), and Bifidobacterium breve (29%)) and FF (Klebsiella pneumoniae (44.1%), Lactobacillus rhamnosus (29.4%), and Bifidobacterium longum (26.5%)) infants were used. Caco-2 monolayers grown in a transwell cell-culture system (12mm inserts (Millipore)) were challenged by apical addition of 2 · 106cfu/insert ofbacteria. PBMCs (1 · 106 cells/well) and gluten specific T cell clones (1 · 105 cells/well) from HLA-DQ2 patients were added in the basal compartment of the culture well for a 12-hour incubation.Gliadin (7.5 mg/mL) was also added at the same time in the basal or apical compartment. Thereafter, further 36 hours incubation was allowed after disassembly of the system in order to measure the cytokine production by the sensitized Caco-2, and cytokine production and proliferation by T cell clones separately.TNF-a, IL-6, IL-1b, and IL-8 cytokines were measured in Caco-2 cells basolateral medium, and TNF-a, IL-6, IL-1b, and IL-10 cytokines were measured in T cells supernatant by Cytometric Bead Array Flex sets (BD Biosciences) and analyzed by flow cytometry. T cell proliferation was measured by quantification of H3-thymidine incorporation. Gliadin in the apical compartment did not show any effect on T cell proliferation and cytokine production. In the basal compartment Gliadin plus breastfed mixture (Gli-BF) showed a lower T cell proliferation than gliadin plus formula-fed mixture (Gli-FF) and gliadin alone. IL-10 in T cell supernatants, and IL-1b in Caco-2 supernatants were below the minimum detectable concentration in all conditions.Gliadin, Gli-BF and Gli-FF induced cytokine secretion compared to control without gliadin, however the BF mixture inhibited the production of IL-6 and TNF-bcompared to Gli-FF and gliadin alone. When the bacteria combination plus gliadin were cultured in direct contact with the PBMC and T cells and no Caco-2 cells, the inhibition of cytokine production by theBF bacteria combination compared to gliadin alone was also observed, while FF combination did not reduce cytokine production and proliferation.We suggest that certain bacteria combinations, as observed with those more prevalent in feces from breast fed infants, might attenuated the effect of gliadin onT-cell proliferation and cytokine production.es_ES
dc.description.sponsorshipThis work was supported by grants AGL2007¿66126-C03¿01/ALI and 03/ALI from the Spanish Ministry of Science and Innovationes_ES
dc.language.isoenges_ES
dc.publisherCambridge University Presses_ES
dc.rightsopenAccesses_ES
dc.titleBacterial immune modulation of the cytokine response elicited by gliadin in an in vitro model ofceliac diseasees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1017/S0029665113000736-
dc.description.peerreviewedPeer reviewedes_ES
dc.identifier.e-issn1475-2719-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.openairetypeartículo-
item.cerifentitytypePublications-
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