Abstract
Chronic Rhinosinusitis (CRS), a chronic upper airway inflammation, is an inflammation of the nose and the paranasal cavities and is highly prevalent. Chronic rhinosinusitis is currently classified as CRS with nasal polyps or CRS without nasal polyps. This review highlights the pathophysiological differences in CRS on remodeling and on T-cell patterns. Nasal polyps have a high co-morbidity with the lower airway inflammatory disease, asthma. Evidence is accumulating for the role of superantigens, Staphylococcus aureus enterotoxins, in CRS with nasal polyps and asthma, both T helper 2 –biased diseases. Until today there are no biomarkers involved in the diagnosis of CRS or the treatment follow-up. Further differentiation of the phenotype of the disease is needed, which will reflect in the development of new biomarkers and in new innovative treatment options. Defining and predicting response to therapy in individual CRS patients is a challenge for future research.
Keywords: Chronic rhinosinusitis, asthma, inflammation, treatment
Current Pharmaceutical Design
Title:Local Inflammation in Chronic Upper Airway Disease
Volume: 18 Issue: 16
Author(s): Lien Calus, Thibaut Van Zele, Lara Derycke, Olga Krysko, Tineke Dutre, Peter Tomassen, Melissa Dullaers, Claus Bachert and Philippe Gevaert
Affiliation:
Keywords: Chronic rhinosinusitis, asthma, inflammation, treatment
Abstract: Chronic Rhinosinusitis (CRS), a chronic upper airway inflammation, is an inflammation of the nose and the paranasal cavities and is highly prevalent. Chronic rhinosinusitis is currently classified as CRS with nasal polyps or CRS without nasal polyps. This review highlights the pathophysiological differences in CRS on remodeling and on T-cell patterns. Nasal polyps have a high co-morbidity with the lower airway inflammatory disease, asthma. Evidence is accumulating for the role of superantigens, Staphylococcus aureus enterotoxins, in CRS with nasal polyps and asthma, both T helper 2 –biased diseases. Until today there are no biomarkers involved in the diagnosis of CRS or the treatment follow-up. Further differentiation of the phenotype of the disease is needed, which will reflect in the development of new biomarkers and in new innovative treatment options. Defining and predicting response to therapy in individual CRS patients is a challenge for future research.
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Cite this article as:
Calus Lien, Van Zele Thibaut, Derycke Lara, Krysko Olga, Dutre Tineke, Tomassen Peter, Dullaers Melissa, Bachert Claus and Gevaert Philippe, Local Inflammation in Chronic Upper Airway Disease, Current Pharmaceutical Design 2012; 18 (16) . https://dx.doi.org/10.2174/138161212800166022
DOI https://dx.doi.org/10.2174/138161212800166022 |
Print ISSN 1381-6128 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-4286 |
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