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dc.date.accessioned 2019-11-29T14:28:11Z
dc.date.available 2019-11-29T14:28:11Z
dc.date.issued 2015
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/86366
dc.description.abstract Celiac Disease (CD) is an interferon (IFN)γ-mediated duodenal hypersensitivity to wheat gluten occurring in genetically predisposed individuals. Gluten-free diet (GFD) leads to a complete remission of the disease. Vα24-restricted invariant NKT (iNKT) cells are important to maintain immune homeostasis in the gut mucosa because of their unique capacity to rapidly produce large quantities of both T-helper (Th)1 and Th2 cytokines upon stimulation. We studied the presence of these cells in the CD duodenum. Duodenal biopsies were obtained from 45 untreated-CD patients (uCD), 15 Gluten Free Diet-CD patients (GFD-CD), 44 non-inflamed non-CD controls (C-controls) and 15 inflamed non-CD controls (I-controls). Two populations from Spain and Argentina were recruited. Messenger RNA (mRNA) expression of Vα24-Jα18 (invariant TCRα chain of human iNKT cells), IFNγ and intracellular transcription factor Forkhead Box P3 (Foxp3), and flow cytometry intraepithelial lymphocyte (IEL) profile were determined. Both uCD and GFD-CD patients had higher Vα24-Jα18 mRNA levels than non-CD controls (I and C-controls). The expression of Vα24-Jα18 correlated with Marsh score for the severity of mucosal lesion and also with increased mRNA IFNγ levels. uCD and GFD-CD patients had decreased mRNA expression of FoxP3 but increased expression of Vα24-Jα18, which revealed a CD-like molecular profile. Increased numbers of iNKT cells were confirmed by flow cytometry within the intraepithelial lymphocyte compartment of uCD and GFD-CD patients and correlated with Vα24-Jα18 mRNA expression. In conclusion, we have found an increased number of iNKT cells in the duodenum from both uCD and GFD-CD patients, irrespective of the mucosal status. A CD-like molecular profile, defined by an increased mRNA expression of Vα24-Jα18 together with a decreased expression of FoxP3, may represent a pro-inflammatory signature of the CD duodenum. en
dc.format.extent 8960-8976 es
dc.language en es
dc.subject Celiac disease es
dc.subject Celiac disease-like molecular profile es
dc.subject IFNγ es
dc.subject INKT es
dc.subject Intraepithelial lymphocytes es
dc.subject Vα24-Jα18 es
dc.title Increased intraepithelial Vα24 invariant NKT cells in the celiac duodenum en
dc.type Articulo es
sedici.identifier.other doi:10.3390/nu7115444 es
sedici.identifier.other eid:2-s2.0-84946084518 es
sedici.identifier.issn 2072-6643 es
sedici.creator.person Montalvillo, Enrique es
sedici.creator.person Bernardo, David es
sedici.creator.person Martínez Abad, Beatriz es
sedici.creator.person Allegretti, Yessica Lorena es
sedici.creator.person Fernández Salazar, Luis es
sedici.creator.person Calvo, Carmen es
sedici.creator.person Chirdo, Fernando Gabriel es
sedici.creator.person Garrote, José A. es
sedici.creator.person Arranz, Eduardo es
sedici.subject.materias Ciencias Exactas es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Exactas es
mods.originInfo.place Laboratorio de Investigaciones del Sistema Inmune es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 4.0 International (CC BY 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Nutrients es
sedici.relation.journalVolumeAndIssue vol. 7, no. 11 es
sedici.rights.sherpa * Color: green * Pre-print del autor: can * Post-print del autor: can * Versión de editor/PDF:can * Condiciones: >>On open access repositories >>Publisher's version/PDF may be used >>Published source must be acknowledged >>Creative Commons Attribution License 4.0 >>Authors retain copyright >>Authors are encouraged to submit their published articles to institutional repositories >>All titles are open access journals * Link a Sherpa: http://sherpa.ac.uk/romeo/issn/2072-6643/es/


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Creative Commons Attribution 4.0 International (CC BY 4.0) Except where otherwise noted, this item's license is described as Creative Commons Attribution 4.0 International (CC BY 4.0)