MycoBiomDB – Record Details (MyCo_3299)

Biomarker Record Details

Database ID: MyCo_3299
DB IDMyCo_3299
TitleIncreased sensitivity to IL-4 in patients with allergic bronchopulmonary aspergillosis
Year2000
PMID11146389
Fungal Diseases involvedAllergic bronchopulmonary aspergillosis
Associated Medical ConditionNone
GenusAspergillus
Speciesfumigatus
OrganismAspergillus fumigatus
Ethical StatementPatient involvement in the study was approved by the St. Louis University Institutional Review Board.
Site of InfectionNone
Opportunistic invasiveNone
Sample typeBody fluid
Sample sourceBlood
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameCD86
Biomarker Full NameCD86
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationUSA
CohortThree groups of patients, ABPA, atopic and nonatopic, were studied , there were 10 patients with ABPA, 4 with asthma and 6 with CF.
Cohort No.20
Age GroupAug-76
P Valuep<0.001
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismAllergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity lung disease mediated by an allergic late- phase inflammatory response to Aspergillus fumigatus antigens characterized by markedly elevated A. fumigatus-specific and total IgE levels and eosinophilia, and manifested by wheezing, pulmonary infiltrates and pul- monary bronchiectasis and fibrosis. Previously we reported that there was an IL-4-dependent autocrine Th2 CD4+ T cell response to an Aspergillus allergen, Asp f 1. In addition, ABPA patients’ B cells spontaneously synthesized and secreted IgE. Recently, immunogenet- ics studies implicating HLA-DR2 and DR5 restriction have further contributed to the understanding of the immunopathogenesis of why certain individuals are sus- pectible to develop ABPA. However, ABPA afflicts only a small percentage of susceptible atopic individuals with either asthma or cystic fibrosis.
TechniqueAnalytic
Analysis MethodFlow Cytometry Analysis
ELISA kitsNone
Assay DataNone
Validation Techniques usedELISA, Flow Cytometry Analysis
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone