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Update on host-pathogen interactions in cystic fibrosis lung disease
Bacterial and fungal infections are hallmarks of cystic fibrosis (CF) lung disease. In the era of long-term inhaled antibiotics and increasing CF patient survival, new “emerging” pathogens are detected in CF airways, yet their pathophysiological disease relevance remains largely controversial and in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764602/ https://www.ncbi.nlm.nih.gov/pubmed/26905568 http://dx.doi.org/10.1186/s40348-016-0039-5 |
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author | Hector, Andreas Frey, Nina Hartl, Dominik |
author_facet | Hector, Andreas Frey, Nina Hartl, Dominik |
author_sort | Hector, Andreas |
collection | PubMed |
description | Bacterial and fungal infections are hallmarks of cystic fibrosis (CF) lung disease. In the era of long-term inhaled antibiotics and increasing CF patient survival, new “emerging” pathogens are detected in CF airways, yet their pathophysiological disease relevance remains largely controversial and incompletely defined. As a response to chronic microbial triggers, innate immune cells, particularly neutrophils, are continuously recruited into CF airways where they combat pathogens but also cause tissue injury through release of oxidants and proteases. The coordinated interplay between host immune cell activation and pathogens is essential for the outcome of CF lung disease. Here, we provide a concise overview and update on host-pathogen interactions in CF lung disease. |
format | Online Article Text |
id | pubmed-4764602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47646022016-03-29 Update on host-pathogen interactions in cystic fibrosis lung disease Hector, Andreas Frey, Nina Hartl, Dominik Mol Cell Pediatr Mini Review Bacterial and fungal infections are hallmarks of cystic fibrosis (CF) lung disease. In the era of long-term inhaled antibiotics and increasing CF patient survival, new “emerging” pathogens are detected in CF airways, yet their pathophysiological disease relevance remains largely controversial and incompletely defined. As a response to chronic microbial triggers, innate immune cells, particularly neutrophils, are continuously recruited into CF airways where they combat pathogens but also cause tissue injury through release of oxidants and proteases. The coordinated interplay between host immune cell activation and pathogens is essential for the outcome of CF lung disease. Here, we provide a concise overview and update on host-pathogen interactions in CF lung disease. Springer Berlin Heidelberg 2016-02-23 /pmc/articles/PMC4764602/ /pubmed/26905568 http://dx.doi.org/10.1186/s40348-016-0039-5 Text en © Hector et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Mini Review Hector, Andreas Frey, Nina Hartl, Dominik Update on host-pathogen interactions in cystic fibrosis lung disease |
title | Update on host-pathogen interactions in cystic fibrosis lung disease |
title_full | Update on host-pathogen interactions in cystic fibrosis lung disease |
title_fullStr | Update on host-pathogen interactions in cystic fibrosis lung disease |
title_full_unstemmed | Update on host-pathogen interactions in cystic fibrosis lung disease |
title_short | Update on host-pathogen interactions in cystic fibrosis lung disease |
title_sort | update on host-pathogen interactions in cystic fibrosis lung disease |
topic | Mini Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764602/ https://www.ncbi.nlm.nih.gov/pubmed/26905568 http://dx.doi.org/10.1186/s40348-016-0039-5 |
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