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dc.contributor.author
Montalvillo, Enrique  
dc.contributor.author
Bernardo, David  
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Martínez Abad, Beatriz  
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Allegretti, Yessica Lorena  
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Fernández Salazar, Luis  
dc.contributor.author
Calvo, Carmen  
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Chirdo, Fernando Gabriel  
dc.contributor.author
Garrote, José A.  
dc.contributor.author
Arranz, Eduardo  
dc.date.available
2018-08-07T16:58:38Z  
dc.date.issued
2015-10  
dc.identifier.citation
Montalvillo, Enrique; Bernardo, David; Martínez Abad, Beatriz; Allegretti, Yessica Lorena; Fernández Salazar, Luis; et al.; Increased intraepithelial Vα24 invariant NKT cells in the celiac duodenum; MDPI AG; Nutrients; 7; 11; 10-2015; 8960-8976  
dc.identifier.issn
2072-6643  
dc.identifier.uri
http://hdl.handle.net/11336/54435  
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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
MDPI AG  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Celiac Disease  
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Celiac Disease-Like Molecular Profile  
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IfnΓ  
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Inkt  
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Intraepithelial Lymphocytes  
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VΑ24-JΑ18  
dc.subject.classification
Inmunología  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Increased intraepithelial Vα24 invariant NKT cells in the celiac duodenum  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-08-02T15:32:05Z  
dc.journal.volume
7  
dc.journal.number
11  
dc.journal.pagination
8960-8976  
dc.journal.pais
Suiza  
dc.journal.ciudad
Bazel  
dc.description.fil
Fil: Montalvillo, Enrique. Universidad de Valladolid; España. Consejo Superior de Investigaciones Científicas; España  
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Fil: Bernardo, David. Imperial College London; Reino Unido. Hospital Universitario de La Princesa ; Países Bajos  
dc.description.fil
Fil: Martínez Abad, Beatriz. Universidad de Valladolid; España. Consejo Superior de Investigaciones Científicas; España. Instituto de Investigación Sanitaria Princesa; España  
dc.description.fil
Fil: Allegretti, Yessica Lorena. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias Biológicas. Laboratorio de Investigaciones del Sistema Inmune; Argentina  
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Fil: Fernández Salazar, Luis. Hospital Clínico Universitario; España  
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Fil: Calvo, Carmen. Hospital Clínico Universitario; España  
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Fil: Chirdo, Fernando Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias Biológicas. Laboratorio de Investigaciones del Sistema Inmune; Argentina  
dc.description.fil
Fil: Garrote, José A.. Universidad de Valladolid; España. Consejo Superior de Investigaciones Científicas; España. Hospital Universitario Rio Hortega; España  
dc.description.fil
Fil: Arranz, Eduardo. Universidad de Valladolid; España. Consejo Superior de Investigaciones Científicas; España  
dc.journal.title
Nutrients  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.3390/nu7115444  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.mdpi.com/2072-6643/7/11/5444