Allergic bronchopulmonary aspergillosis

Allergic bronchopulmonary aspergillosis (ABPA) occurs in nonimmunocompromised patients and belongs to the hypersensitivity disorders induced by Aspergillus. Genetic factors and activation of bronchial epithelial cells in asthma or cystic fibrosis are responsible for the development of a CD4+Th2 lymp...

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Published inAllergy (Copenhagen) Vol. 60; no. 8; pp. 1004 - 1013
Main Authors Tillie‐Leblond, I., Tonnel, A.‐B.
Format Journal Article
LanguageEnglish
Published Oxford, UK Munksgaard International Publishers 01.08.2005
Blackwell
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Summary:Allergic bronchopulmonary aspergillosis (ABPA) occurs in nonimmunocompromised patients and belongs to the hypersensitivity disorders induced by Aspergillus. Genetic factors and activation of bronchial epithelial cells in asthma or cystic fibrosis are responsible for the development of a CD4+Th2 lymphocyte activation and IgE, IgG and IgA‐AF antibodies production. The diagnosis of ABPA is based on the presence of a combination of clinical, biological and radiological criteria. The severity of the disease is related to corticosteroid‐dependant asthma or/and diffuse bronchiectasis with fibrosis. The treatment is based on oral corticosteroids for 6–8 weeks at acute phase or exacerbation and itraconazole is now recommended and validated at a dose of 200 mg/day for a duration of 16 weeks.
Bibliography:Present address: Unité INSERM U416, Institut Pasteur, and Department of Lung Disease and of Immuno‐Allergology, Lille, France
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ISSN:0105-4538
1398-9995
DOI:10.1111/j.1398-9995.2005.00887.x