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Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet

Celiac disease (CD) is a systemic disorder characterized by an immune-mediated reaction to gluten and a wide spectrum of clinical manifestations. Currently, the main treatment of CD is represented by adherence to a gluten-free diet (GFD) which determines the resolution of symptoms, and the normaliza...

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Autores principales: Sangineto, Moris, Graziano, Giusi, D’Amore, Simona, Salvia, Roberto, Palasciano, Giuseppe, Sabbà, Carlo, Vacca, Michele, Cariello, Marica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967809/
https://www.ncbi.nlm.nih.gov/pubmed/29795662
http://dx.doi.org/10.1371/journal.pone.0197915
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author Sangineto, Moris
Graziano, Giusi
D’Amore, Simona
Salvia, Roberto
Palasciano, Giuseppe
Sabbà, Carlo
Vacca, Michele
Cariello, Marica
author_facet Sangineto, Moris
Graziano, Giusi
D’Amore, Simona
Salvia, Roberto
Palasciano, Giuseppe
Sabbà, Carlo
Vacca, Michele
Cariello, Marica
author_sort Sangineto, Moris
collection PubMed
description Celiac disease (CD) is a systemic disorder characterized by an immune-mediated reaction to gluten and a wide spectrum of clinical manifestations. Currently, the main treatment of CD is represented by adherence to a gluten-free diet (GFD) which determines the resolution of symptoms, and the normalization of the serology and of the duodenal villous atrophy. In the present study, we aimed to identify changes in gene expression in peripheral blood mononuclear cells (PBMCs) of celiac patients on GFD for at least 2 years, in order to identify novel disease biomarkers and candidate targets for putative therapeutic approaches. Microarray analysis was performed on PBMCs from 17 celiac patients on long-term GFD and 20 healthy controls. We identified 517 annotated genes that were significantly modulated between celiac patients and controls. Significant biological pathways were functionally clustered using the Core Function of Ingenuity System Pathway Analysis (IPA). Intriguingly, despite being on a GFD, celiac patients exhibited a peculiar PBMC profile characterized by an aberrant expression of genes involved in the regulation of immunity, inflammatory response, metabolism, and cell proliferation. Random forest algorithm was then used to validate the prediction ability of core genes as classifiers of the “celiac status”. In conclusion, our study identified a characteristic PBMCs signature profile in clinically asymptomatic celiac patient.
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spelling pubmed-59678092018-06-08 Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet Sangineto, Moris Graziano, Giusi D’Amore, Simona Salvia, Roberto Palasciano, Giuseppe Sabbà, Carlo Vacca, Michele Cariello, Marica PLoS One Research Article Celiac disease (CD) is a systemic disorder characterized by an immune-mediated reaction to gluten and a wide spectrum of clinical manifestations. Currently, the main treatment of CD is represented by adherence to a gluten-free diet (GFD) which determines the resolution of symptoms, and the normalization of the serology and of the duodenal villous atrophy. In the present study, we aimed to identify changes in gene expression in peripheral blood mononuclear cells (PBMCs) of celiac patients on GFD for at least 2 years, in order to identify novel disease biomarkers and candidate targets for putative therapeutic approaches. Microarray analysis was performed on PBMCs from 17 celiac patients on long-term GFD and 20 healthy controls. We identified 517 annotated genes that were significantly modulated between celiac patients and controls. Significant biological pathways were functionally clustered using the Core Function of Ingenuity System Pathway Analysis (IPA). Intriguingly, despite being on a GFD, celiac patients exhibited a peculiar PBMC profile characterized by an aberrant expression of genes involved in the regulation of immunity, inflammatory response, metabolism, and cell proliferation. Random forest algorithm was then used to validate the prediction ability of core genes as classifiers of the “celiac status”. In conclusion, our study identified a characteristic PBMCs signature profile in clinically asymptomatic celiac patient. Public Library of Science 2018-05-24 /pmc/articles/PMC5967809/ /pubmed/29795662 http://dx.doi.org/10.1371/journal.pone.0197915 Text en © 2018 Sangineto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sangineto, Moris
Graziano, Giusi
D’Amore, Simona
Salvia, Roberto
Palasciano, Giuseppe
Sabbà, Carlo
Vacca, Michele
Cariello, Marica
Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title_full Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title_fullStr Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title_full_unstemmed Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title_short Identification of peculiar gene expression profile in peripheral blood mononuclear cells (PBMC) of celiac patients on gluten free diet
title_sort identification of peculiar gene expression profile in peripheral blood mononuclear cells (pbmc) of celiac patients on gluten free diet
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967809/
https://www.ncbi.nlm.nih.gov/pubmed/29795662
http://dx.doi.org/10.1371/journal.pone.0197915
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