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Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients

Eosinophilic esophagitis (EoE) is a chronic inflammatory condition of the esophagus characterized by increased number of eosinophils. Currently, EoE diagnosis is based on endoscopic procedures for histopathological examination, eosinophils’ counting and, often, in clinical practice, the challenge is...

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Autores principales: de Souza, Tafarel Andrade, Carneiro, Ana Paula, Narciso, Andreia S., Barros, Cristina P., Alves, Douglas Alexsander, Marson, Luciane B., Tunala, Tatiane, de Alcântara, Tânia M., de Paiva Maia, Yara Cristina, Briza, Peter, Ferreira, Fatima, Goulart, Luiz R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289663/
https://www.ncbi.nlm.nih.gov/pubmed/35851408
http://dx.doi.org/10.1038/s41598-022-16293-1
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author de Souza, Tafarel Andrade
Carneiro, Ana Paula
Narciso, Andreia S.
Barros, Cristina P.
Alves, Douglas Alexsander
Marson, Luciane B.
Tunala, Tatiane
de Alcântara, Tânia M.
de Paiva Maia, Yara Cristina
Briza, Peter
Ferreira, Fatima
Goulart, Luiz R.
author_facet de Souza, Tafarel Andrade
Carneiro, Ana Paula
Narciso, Andreia S.
Barros, Cristina P.
Alves, Douglas Alexsander
Marson, Luciane B.
Tunala, Tatiane
de Alcântara, Tânia M.
de Paiva Maia, Yara Cristina
Briza, Peter
Ferreira, Fatima
Goulart, Luiz R.
author_sort de Souza, Tafarel Andrade
collection PubMed
description Eosinophilic esophagitis (EoE) is a chronic inflammatory condition of the esophagus characterized by increased number of eosinophils. Currently, EoE diagnosis is based on endoscopic procedures for histopathological examination, eosinophils’ counting and, often, in clinical practice, the challenge is the differentiation between EoE and gastroesophageal reflux disease (GERD). Our aim was to develop novel peptide ligand to Eosinophil cationic protein (ECP) present in EoE biopsies of patients with potential to be used for detection. We performed a comparative proteomic analysis using liquid chromatography-tandem mass spectrometry (LC–MS/MS) of esophageal biopsies from pediatric patients with eosinophilic esophagitis, gastroesophageal reflux disease and control individuals. Then, phage display technology was used to select peptides against specific up-regulated protein from EoE patients. Twelve phage clones were selected after three biopanning rounds, and the best phage clone reactivity was evaluated by phage-ELISA assay using esophageal mucus samples from 94 pediatric patients. Mass spectrometry showed that eosinophil cationic protein (ECP) was one of the most up-regulated proteins in EoE patients, which is an eosinophil granule protein usually deposited on tissues to mediate remodeling, but in excess may cause fibrosis and hypertrophy, especially in allergic responses. A highly reactive ECP-ligand peptide (E5) was able to distinguish reactive mucus of EoE patients from GERD and the control individuals by Phage-ELISA, achieving a sensitivity of 84.62%, and a specificity of 82.72%. This is the first study that successfully demonstrated an antibody-like peptide targeting ECP at the esophagus mucus as a useful auxilliary tool for EoE diagnosis with a significant association with atopic disorders and dysphagia. ClinicalTrials.gov no.: NCT03069573.
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spelling pubmed-92896632022-07-18 Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients de Souza, Tafarel Andrade Carneiro, Ana Paula Narciso, Andreia S. Barros, Cristina P. Alves, Douglas Alexsander Marson, Luciane B. Tunala, Tatiane de Alcântara, Tânia M. de Paiva Maia, Yara Cristina Briza, Peter Ferreira, Fatima Goulart, Luiz R. Sci Rep Article Eosinophilic esophagitis (EoE) is a chronic inflammatory condition of the esophagus characterized by increased number of eosinophils. Currently, EoE diagnosis is based on endoscopic procedures for histopathological examination, eosinophils’ counting and, often, in clinical practice, the challenge is the differentiation between EoE and gastroesophageal reflux disease (GERD). Our aim was to develop novel peptide ligand to Eosinophil cationic protein (ECP) present in EoE biopsies of patients with potential to be used for detection. We performed a comparative proteomic analysis using liquid chromatography-tandem mass spectrometry (LC–MS/MS) of esophageal biopsies from pediatric patients with eosinophilic esophagitis, gastroesophageal reflux disease and control individuals. Then, phage display technology was used to select peptides against specific up-regulated protein from EoE patients. Twelve phage clones were selected after three biopanning rounds, and the best phage clone reactivity was evaluated by phage-ELISA assay using esophageal mucus samples from 94 pediatric patients. Mass spectrometry showed that eosinophil cationic protein (ECP) was one of the most up-regulated proteins in EoE patients, which is an eosinophil granule protein usually deposited on tissues to mediate remodeling, but in excess may cause fibrosis and hypertrophy, especially in allergic responses. A highly reactive ECP-ligand peptide (E5) was able to distinguish reactive mucus of EoE patients from GERD and the control individuals by Phage-ELISA, achieving a sensitivity of 84.62%, and a specificity of 82.72%. This is the first study that successfully demonstrated an antibody-like peptide targeting ECP at the esophagus mucus as a useful auxilliary tool for EoE diagnosis with a significant association with atopic disorders and dysphagia. ClinicalTrials.gov no.: NCT03069573. Nature Publishing Group UK 2022-07-18 /pmc/articles/PMC9289663/ /pubmed/35851408 http://dx.doi.org/10.1038/s41598-022-16293-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
de Souza, Tafarel Andrade
Carneiro, Ana Paula
Narciso, Andreia S.
Barros, Cristina P.
Alves, Douglas Alexsander
Marson, Luciane B.
Tunala, Tatiane
de Alcântara, Tânia M.
de Paiva Maia, Yara Cristina
Briza, Peter
Ferreira, Fatima
Goulart, Luiz R.
Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title_full Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title_fullStr Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title_full_unstemmed Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title_short Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
title_sort eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289663/
https://www.ncbi.nlm.nih.gov/pubmed/35851408
http://dx.doi.org/10.1038/s41598-022-16293-1
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