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Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis
The respiratory epithelium represents the first chemical, immune, and physical barrier against inhaled noxious materials, particularly pathogens in cystic fibrosis. Local mucus thickening, altered mucociliary clearance, and reduced pH due to CFTR protein dysfunction favor bacterial overgrowth and ex...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700636/ https://www.ncbi.nlm.nih.gov/pubmed/34944110 http://dx.doi.org/10.3390/cells10123603 |
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author | Gohy, Sophie Moeremans, Alexandra Pilette, Charles Collin, Amandine |
author_facet | Gohy, Sophie Moeremans, Alexandra Pilette, Charles Collin, Amandine |
author_sort | Gohy, Sophie |
collection | PubMed |
description | The respiratory epithelium represents the first chemical, immune, and physical barrier against inhaled noxious materials, particularly pathogens in cystic fibrosis. Local mucus thickening, altered mucociliary clearance, and reduced pH due to CFTR protein dysfunction favor bacterial overgrowth and excessive inflammation. We aimed in this review to summarize respiratory mucosal alterations within the epithelium and current knowledge on local immunity linked to immunoglobulin A in patients with cystic fibrosis. |
format | Online Article Text |
id | pubmed-8700636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87006362021-12-24 Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis Gohy, Sophie Moeremans, Alexandra Pilette, Charles Collin, Amandine Cells Review The respiratory epithelium represents the first chemical, immune, and physical barrier against inhaled noxious materials, particularly pathogens in cystic fibrosis. Local mucus thickening, altered mucociliary clearance, and reduced pH due to CFTR protein dysfunction favor bacterial overgrowth and excessive inflammation. We aimed in this review to summarize respiratory mucosal alterations within the epithelium and current knowledge on local immunity linked to immunoglobulin A in patients with cystic fibrosis. MDPI 2021-12-20 /pmc/articles/PMC8700636/ /pubmed/34944110 http://dx.doi.org/10.3390/cells10123603 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gohy, Sophie Moeremans, Alexandra Pilette, Charles Collin, Amandine Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title | Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title_full | Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title_fullStr | Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title_full_unstemmed | Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title_short | Immunoglobulin A Mucosal Immunity and Altered Respiratory Epithelium in Cystic Fibrosis |
title_sort | immunoglobulin a mucosal immunity and altered respiratory epithelium in cystic fibrosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700636/ https://www.ncbi.nlm.nih.gov/pubmed/34944110 http://dx.doi.org/10.3390/cells10123603 |
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