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Allergic Bronchopulmonary Aspergillosis in a Patient with Cystic Fibrosis: Diagnostic Criteria when the IgE Level is Less Than 500 IU/mL

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Date 2005 Nov 30
PMID 16312174
Citations 2
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Abstract

Background: Recently, the Cystic Fibrosis Foundation developed a consensus report recommending diagnostic criteria for allergic bronchopulmonary aspergillosis (ABPA) in patients with cystic fibrosis that includes a serum IgE level greater than 500 IU/mL as the "minimal diagnostic criterion."

Objective: To describe a 7-year-old girl with ABPA whose serum IgE level increased to only 398 IU/mL.

Methods: Total IgE and anti-Aspergillus serologic measurements were performed using enzyme-linked immunosorbent assay and standard laboratory techniques; HLA analysis was performed; interleukin 4 receptor alpha single nucleotide polymorphisms were performed using polymerase chain reaction and DNA sequencing; CD23+ B cells were measured using flow cytometry; and cytokine synthesis to Aspergillus purified antigens was assessed using flow cytometry.

Results: A 7-year-old girl with cystic fibrosis who had mild pulmonary disease and well-controlled asthma developed pulmonary infiltrates, increased wheezing, and decreased pulmonary function. Additional studies demonstrated peripheral blood eosinophilia (eosinophil count, 1807 cells/mm3 [19%]) and an increase in IgE and IgG anti-Aspergillus serology; bronchoalveolar lavage revealed septate hyphae with 45 degrees branching subsequently identified as A fumigatus and pulmonary eosinophilia. Previous HLA typing revealed that the patient was HLA-DR2+, DRB*1501, HLA-DQ2-, a pattern associated with increased risk of ABPA. In addition, there was increased up-regulation of CD23 molecules by interleukin 4 stimulation on the patient's B cells, as observed in ABPA. The patient was treated with corticosteroids and itraconazole with resolution of symptoms and pulmonary infiltrates.

Conclusions: Examination of the pulmonary inflammatory response using bronchoalveolar lavage, genetic risk with HLA-DR2+DQ2- typing, and increased interleukin 4 sensitivity are useful adjunctive studies in the diagnosis of ABPA.

Citing Articles

Recombinant allergens combined with biological markers in the diagnosis of allergic bronchopulmonary aspergillosis in cystic fibrosis patients.

Fricker-Hidalgo H, Coltey B, Llerena C, Renversez J, Grillot R, Pin I Clin Vaccine Immunol. 2010; 17(9):1330-6.

PMID: 20631331 PMC: 2944470. DOI: 10.1128/CVI.00200-10.


IL-4 alpha chain receptor (IL-4Ralpha) polymorphisms in allergic bronchopulmonary sspergillosis.

Knutsen A, Kariuki B, Consolino J, Warrier M Clin Mol Allergy. 2006; 4:3.

PMID: 16503977 PMC: 1403796. DOI: 10.1186/1476-7961-4-3.