MycoBiomDB – Record Details (MyCo_5962)

Biomarker Record Details

Database ID: MyCo_5962
DB IDMyCo_5962
TitleRecombinant allergens combined with biological markers in the diagnosis of allergic bronchopulmonary aspergillosis in cystic fibrosis patients
Year2010
PMID20631331
Fungal Diseases involvedAllergic bronchopulmonary aspergillosis
Associated Medical ConditionCystic fibrosis
GenusAspergillus
Speciesfumigatus
OrganismAspergillus fumigatus
Ethical StatementNone
Site of InfectionLungs
Opportunistic invasiveOpportunistic
Sample typeBody fluid
Sample sourceSerum
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NamerAspf4 IgE
Biomarker Full NameA. fumigatus recombinant allergens rAspf4 Immunoglobulin E
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationFrance
CohortIn our retrospective study, a total of 133 sera from 65 patients (30 males and 35 females; mean age, 13.2 9.9 years; range, 1 to 53 years of age) with cystic fibrosis, regularly followed up at the Grenoble cystic fibrosis center between 1997 and 2008, were analyzed.
Cohort No.65
Age Group1 to 53 years of age
P Valuep<0.05
Sensitivity0.923
Specificity0.937
Positive Predictive Value0.8
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismAllergic bronchopulmonary aspergillosis (ABPA) is a frequent complication in patients with cystic fibrosis that causes significant respiratory morbidity. The exact prevalence of ABPA is not clearly known; however, it ranges from 2 to 25% in patients with cystic fibrosis. ABPA may lead to acute worsening of the respiratory condition and ongoing decline in lung function. Without adequate treatment, ABPA ultimately progresses to a chronic state with lung fibrosis. ABPA is a hypersensitivity pulmonary disease associated with inflammatory destruction of airways in response to Aspergillus allergens. Thus, chronic airway colonization with Aspergillus induces strong inflammatory responses with high IgE levels. The factors leading to ABPA are not clearly understood, but it is believed that Aspergillus-specific, IgE mediated type I hypersensitivity reactions and specific IgG-mediated type III hypersensitivity reactions play central roles in the pathogenesis of ABPA. Furthermore, host factors, including individual susceptibility, may contribute to the immunopathogenesis of ABPA. Early diagnosis and treatment of ABPA are important to prevent serious and potentially irreversible lung damage.
TechniqueAnalytic
Analysis MethodPharmacia UniCAP Based
ELISA kitsNone
Assay DataNone
Validation Techniques usedPharmacia UniCAP method, ELISA
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone