2000
DOI: 10.1164/ajrccm.162.supplement_1.maic-2
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The Role of Inflammation in Airway Disease

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Cited by 66 publications
(49 citation statements)
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References 59 publications
(78 reference statements)
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“…Airway hyperreactivity is a pathophysiologic response to multiple stimuli released from peribronchial inflammatory cells. Eosinophil recruitment is prominent throughout the response to allergens, and mediators released by these cells foster the development of irreversible airway remodeling (32,33). Lymphocytes and APCs contribute through the Th2-driven production of allergen-specific IgE Abs in secondary lymphoid organs.…”
Section: Discussionmentioning
confidence: 99%
“…Airway hyperreactivity is a pathophysiologic response to multiple stimuli released from peribronchial inflammatory cells. Eosinophil recruitment is prominent throughout the response to allergens, and mediators released by these cells foster the development of irreversible airway remodeling (32,33). Lymphocytes and APCs contribute through the Th2-driven production of allergen-specific IgE Abs in secondary lymphoid organs.…”
Section: Discussionmentioning
confidence: 99%
“…This airway remodeling may lead to long-term morbidity, including irreversible airway obstruction. 8,9 Even more notable is the potential for a severe episode of EIB leading to mortality in competitive athletes. Results of a 7-y study by Becker et al 10 reported 61 EIB-related deaths during competition or practice, with 81% of these deaths occurring in athletes Ͻ21 y old.…”
Section: See the Related Editorial On Page 994mentioning
confidence: 99%
“…Airway disease in CF is characterised by mucus plugging, chronic infection and an excessive inflammatory response, leading to peripheral airway changes in the first few months of life [101][102][103][104][105][106][107][108][109][110][111][112][113][114][115][116][117][118][119]. The characteristic airway abnormalities are bronchiectasis, thickening of the airway wall and mucus plugging [97,103,107,[120][121][122][123][124][125][126], as shown in figure 5.…”
Section: Airway Imaging In Cystic Fibrosismentioning
confidence: 99%