PMID- 15668987 OWN - NLM STAT- MEDLINE DCOM- 20050823 LR - 20171116 IS - 1552-4949 (Print) IS - 1552-4949 (Linking) VI - 64 IP - 1 DP - 2005 Mar TI - Flow cytometric analysis of in vitro activated basophils, specific IgE and skin tests in the diagnosis of pollen-associated food allergy. PG - 28-33 AB - BACKGROUND: Specific immunoglobulin E (IgE) and commercially available skin prick tests have been demonstrated to be unreliable methods to diagnose pollen-associated food allergy. To evaluate the predictive value of the basophil activation test (BAT) in pollen-associated food allergy, the apple-mediated oral allergy syndrome (OAS) in patients with birch pollinosis was chosen as a representative model. METHODS: Patients with birch pollen allergy and a history of apple-mediated OAS (OAS(+), n = 29), patients with birch allergic without OAS (OAS(-), n = 22), and healthy controls (HC, n = 10) without birch pollen allergy and OAS were included. Apple IgE was quantified by the CAP FEIA method. Skin prick tests were performed with a Jonagold apple extract. Flow cytometric analysis of basophils activated with the same Jonagold extract was based on double staining with anti-IgE/anti-CD63 monoclonal antibodies. RESULTS: Comparison between OAS(+) subjects and HC showed sensitivities and specificities of 96% and 100% for apple IgE and 88% and 100% for the apple skin prick test, respectively. For the BAT, sensitivity and specificity were 100%. In contrast, when nonresponders on the BAT were considered, sensitivity decreased to 90%. In a separate analysis between OAS(+) and OAS(-) subjects, specificities decreased to 30% for apple IgE and to 80% for the apple skin test, respectively. The BAT reached a sensitivity of 88% and a specificity of 75%. CONCLUSION: Flow cytometry-assisted quantification of in vitro basophil activation seems to be a reliable instrument in the diagnosis of this model of pollen-associated food allergy. In addition, this study reemphasizes that the specificity of diagnostic allergy tests decreases considerably when, apart from HC, control individuals with cross-reactive antibodies are included. FAU - Ebo, Didier G AU - Ebo DG AD - Department of Immunology, Allergology, and Rheumatology, University of Antwerp, Antwerp, Belgium. FAU - Hagendorens, Margo M AU - Hagendorens MM FAU - Bridts, Chris H AU - Bridts CH FAU - Schuerwegh, Annemie J AU - Schuerwegh AJ FAU - De Clerck, Luc S AU - De Clerck LS FAU - Stevens, Wim J AU - Stevens WJ LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cytometry B Clin Cytom JT - Cytometry. Part B, Clinical cytometry JID - 101235690 RN - 0 (Antigens, CD) RN - 0 (CD63 protein, human) RN - 0 (Platelet Membrane Glycoproteins) RN - 0 (Tetraspanin 30) RN - 37341-29-0 (Immunoglobulin E) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Antigens, CD/metabolism MH - Basophils/*immunology/metabolism MH - Betula/immunology MH - Female MH - Flow Cytometry/*methods MH - Food Hypersensitivity/*diagnosis/immunology MH - Humans MH - Immunoglobulin E/*blood MH - Male MH - Malus/immunology MH - Middle Aged MH - Platelet Membrane Glycoproteins/metabolism MH - Pollen/*immunology MH - ROC Curve MH - Sensitivity and Specificity MH - Skin Tests MH - Tetraspanin 30 MH - Up-Regulation/immunology EDAT- 2005/01/26 09:00 MHDA- 2005/08/24 09:00 CRDT- 2005/01/26 09:00 PHST- 2005/01/26 09:00 [pubmed] PHST- 2005/08/24 09:00 [medline] PHST- 2005/01/26 09:00 [entrez] AID - 10.1002/cyto.b.20042 [doi] PST - ppublish SO - Cytometry B Clin Cytom. 2005 Mar;64(1):28-33. doi: 10.1002/cyto.b.20042.