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Potential of anti-inflammatory treatment for cystic fibrosis lung disease

Cystic fibrosis (CF) is the most common life-shortening genetic disorder in Caucasians. With improved diagnosis and treatment, survival has steadily increased. Unfortunately, the overwhelming majority of patients still die from respiratory failure caused by structural damage resulting from airway ob...

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Detalles Bibliográficos
Autores principales: Taylor-Cousar, Jennifer L, Von Kessel, Kelsey A, Young, Robert, Nichols, David P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218732/
https://www.ncbi.nlm.nih.gov/pubmed/22096358
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author Taylor-Cousar, Jennifer L
Von Kessel, Kelsey A
Young, Robert
Nichols, David P
author_facet Taylor-Cousar, Jennifer L
Von Kessel, Kelsey A
Young, Robert
Nichols, David P
author_sort Taylor-Cousar, Jennifer L
collection PubMed
description Cystic fibrosis (CF) is the most common life-shortening genetic disorder in Caucasians. With improved diagnosis and treatment, survival has steadily increased. Unfortunately, the overwhelming majority of patients still die from respiratory failure caused by structural damage resulting from airway obstruction, recurrent infection, and inflammation. Here, we discuss the role of inflammation and the development of anti-inflammatory therapies to treat CF lung disease. The inflammatory host response is the least addressed component of CF airway disease at this time. Current challenges in both preclinical and clinical investigation make the identification of suitable anti-inflammatory drugs more difficult. Despite this, many researchers are making significant progress toward this goal and the CF research community has reason to believe that new therapies will emerge from these efforts.
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spelling pubmed-32187322011-11-17 Potential of anti-inflammatory treatment for cystic fibrosis lung disease Taylor-Cousar, Jennifer L Von Kessel, Kelsey A Young, Robert Nichols, David P J Inflamm Res Review Cystic fibrosis (CF) is the most common life-shortening genetic disorder in Caucasians. With improved diagnosis and treatment, survival has steadily increased. Unfortunately, the overwhelming majority of patients still die from respiratory failure caused by structural damage resulting from airway obstruction, recurrent infection, and inflammation. Here, we discuss the role of inflammation and the development of anti-inflammatory therapies to treat CF lung disease. The inflammatory host response is the least addressed component of CF airway disease at this time. Current challenges in both preclinical and clinical investigation make the identification of suitable anti-inflammatory drugs more difficult. Despite this, many researchers are making significant progress toward this goal and the CF research community has reason to believe that new therapies will emerge from these efforts. Dove Medical Press 2010-08-10 /pmc/articles/PMC3218732/ /pubmed/22096358 Text en © 2010 Taylor-Cousar et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Taylor-Cousar, Jennifer L
Von Kessel, Kelsey A
Young, Robert
Nichols, David P
Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title_full Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title_fullStr Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title_full_unstemmed Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title_short Potential of anti-inflammatory treatment for cystic fibrosis lung disease
title_sort potential of anti-inflammatory treatment for cystic fibrosis lung disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218732/
https://www.ncbi.nlm.nih.gov/pubmed/22096358
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