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Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients

The aim of the study was to characterize the presence of diverse CD4 and CD8 T cell subsets and regulatory cells in peripheral blood and lower oesophageal sphincter (LES) from a young patient with BE/achalasia without treatment versus achalasia group. In order to characterize the circulating cells i...

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Autores principales: Torres-Landa, Samuel, Furuzawa-Carballeda, Janette, Coss-Adame, Enrique, Valdovinos, Miguel A., Alejandro-Medrano, Edgar, Ramos-Ávalos, Bárbara, Martínez-Benítez, Braulio, Torres-Villalobos, Gonzalo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056281/
https://www.ncbi.nlm.nih.gov/pubmed/27752370
http://dx.doi.org/10.1155/2016/5681590
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author Torres-Landa, Samuel
Furuzawa-Carballeda, Janette
Coss-Adame, Enrique
Valdovinos, Miguel A.
Alejandro-Medrano, Edgar
Ramos-Ávalos, Bárbara
Martínez-Benítez, Braulio
Torres-Villalobos, Gonzalo
author_facet Torres-Landa, Samuel
Furuzawa-Carballeda, Janette
Coss-Adame, Enrique
Valdovinos, Miguel A.
Alejandro-Medrano, Edgar
Ramos-Ávalos, Bárbara
Martínez-Benítez, Braulio
Torres-Villalobos, Gonzalo
author_sort Torres-Landa, Samuel
collection PubMed
description The aim of the study was to characterize the presence of diverse CD4 and CD8 T cell subsets and regulatory cells in peripheral blood and lower oesophageal sphincter (LES) from a young patient with BE/achalasia without treatment versus achalasia group. In order to characterize the circulating cells in this patient, a cytometric analysis was performed. LES tissue was evaluated by double-immunostaining procedure. Five healthy blood donors, 5 type achalasia patients, and 5 oesophagus tissue samples (gastrooesophageal junction) from transplant donors were included as control groups. A conspicuous systemic inflammation was determined in BE/achalasia patient and achalasia versus healthy volunteer group. Nonetheless, a predominance of Th22, Th2, IFN-α-producing T cells, Tregs, Bregs, and pDCregs was observed in BE/achalasia patient versus achalasia group. A low percentage of Th1 subset in BE/achalasia versus achalasia group was determined. A noticeable increase in tissue of Th22, Th17, Th2, Tregs, Bregs, and pDCregs was observed in BE/achalasia versus achalasia group. Th1 subset was lower in the BE/achalasia patient versus achalasia group. This study suggests that inflammation is a possible factor in the pathogenesis of BE/achalasia. Further research needs to be performed to understand the specific cause of the correlation between BE and achalasia.
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spelling pubmed-50562812016-10-17 Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients Torres-Landa, Samuel Furuzawa-Carballeda, Janette Coss-Adame, Enrique Valdovinos, Miguel A. Alejandro-Medrano, Edgar Ramos-Ávalos, Bárbara Martínez-Benítez, Braulio Torres-Villalobos, Gonzalo Case Rep Gastrointest Med Case Report The aim of the study was to characterize the presence of diverse CD4 and CD8 T cell subsets and regulatory cells in peripheral blood and lower oesophageal sphincter (LES) from a young patient with BE/achalasia without treatment versus achalasia group. In order to characterize the circulating cells in this patient, a cytometric analysis was performed. LES tissue was evaluated by double-immunostaining procedure. Five healthy blood donors, 5 type achalasia patients, and 5 oesophagus tissue samples (gastrooesophageal junction) from transplant donors were included as control groups. A conspicuous systemic inflammation was determined in BE/achalasia patient and achalasia versus healthy volunteer group. Nonetheless, a predominance of Th22, Th2, IFN-α-producing T cells, Tregs, Bregs, and pDCregs was observed in BE/achalasia patient versus achalasia group. A low percentage of Th1 subset in BE/achalasia versus achalasia group was determined. A noticeable increase in tissue of Th22, Th17, Th2, Tregs, Bregs, and pDCregs was observed in BE/achalasia versus achalasia group. Th1 subset was lower in the BE/achalasia patient versus achalasia group. This study suggests that inflammation is a possible factor in the pathogenesis of BE/achalasia. Further research needs to be performed to understand the specific cause of the correlation between BE and achalasia. Hindawi Publishing Corporation 2016 2016-09-26 /pmc/articles/PMC5056281/ /pubmed/27752370 http://dx.doi.org/10.1155/2016/5681590 Text en Copyright © 2016 Samuel Torres-Landa et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Torres-Landa, Samuel
Furuzawa-Carballeda, Janette
Coss-Adame, Enrique
Valdovinos, Miguel A.
Alejandro-Medrano, Edgar
Ramos-Ávalos, Bárbara
Martínez-Benítez, Braulio
Torres-Villalobos, Gonzalo
Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title_full Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title_fullStr Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title_full_unstemmed Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title_short Barrett's Oesophagus in an Achalasia Patient: Immunological Analysis and Comparison with a Group of Achalasia Patients
title_sort barrett's oesophagus in an achalasia patient: immunological analysis and comparison with a group of achalasia patients
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056281/
https://www.ncbi.nlm.nih.gov/pubmed/27752370
http://dx.doi.org/10.1155/2016/5681590
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