{"doi":"10.1111/all.15907","title":"<scp>EAACI</scp> task force report: A consensus protocol for the basophil activation test for collaboration and external quality assurance","abstract":"To the editor The basophil activation test (BAT) has significant potential as a diagnostic tool to better phenotype and manage patients with IgE-mediated allergies, so that only a small proportion of patients need to be challenged. Sample, reagent, laboratory procedure, analysis protocols, and population characteristics can influence BAT performance.1, 2 Regulatory approval and clinical implementation require extensive standardization of laboratory protocols, cytometer settings, and results interpretation.3 European national authorities require External Quality Assurance (EQA) of the performance of modern diagnostic laboratories by agencies independent of test suppliers to meet ISO 15189:2012, 15189:2013, and 9001:2015. Based on an online survey among 59 responding European laboratories performing BAT in 20174, 5 (Online Supplement; Results of the online survey), a Task Force (TF) was launched in 2018 to create the basis for a BAT-EQA. Round Robins (RR) were organized with seven shipments of two donors each to 7–10 European centers with overnight courier service from Bonn, DE. Each sample was split into two aliquots: (i) To minimize variation, prior to shipment, blood basophils of anonymous donors were activated with 1 μL anti-FcεRI antibody/mL of blood and stabilized with 0.2 mL Transfix (Cytomark, UK) per mL of blood to stabilize activated basophils up to 24 h for staining6; (ii) Fresh blood was included for stimulation and staining at the participating laboratory sites. TF members met after the third shipment to reach consensus on a protocol for BAT (Online Supplement; Proposed SOP for in house BAT). Data analysis started with identification of the relevant region in a scatter plot (Figure 1A), followed by identification of basophils with the relevant markers following different strategies, for instance, using low SSC and CD193 only or CD193/CD123 or CD193/CD203c (Figure 1B). The threshold was set at 2.5% of CD63 expression on resting basophils (Figure 1C). This threshold set on an unstimulated control sample was determined empirically on independent datasets as equal or greater than 2.5% with ROC curves based on data from patients with hypersensitivity to amoxicillin and patients with peanut allergy, (Online supplement, tables S1 and S2). This setting was used to obtain the percentage of CD63+ cells in both centrally preactivated and locally activated blood samples (Figure 1D–F). This proposal, although considered to be more robust by the majority, did not find universal consensus. One laboratory insisted to maintain a threshold “as close to 0% as possible” as their data are based on that approach. Data from participating laboratories analyzed with their proprietary and the above standardized analysis compared well (online supplement, figure S4). >5% CD63+ basophils above that threshold in an activated sample was considered a positive response. The first two RR were used to train participating laboratories in the procedure of the analysis. Data from RR3 to RR7 were comparable. The standard deviation of activation measured at all participating centers was 16.8% in preactivated blood (Figure 1D) compared with 49.2% for samples activated and analyzed locally (Figure 1D), illustrating the utility of using preactivated blood for EQA (p = .03 Wilcoxon signed rank test). In Figure 1F, individual laboratories performance is presented. After transport, activation of EDTA blood is much better than activation of heparin-stabilized blood (p = .0091, Wilcoxon signed rank test). However, as most laboratories used heparin-stabilized blood in daily routine, we developed a method that accommodates both approaches by preactivating blood for EQA. EQA for BAT is critical to facilitate routine implementation of this assay in the field of in vitro allergy diagnostics. The variability of the responses to our survey highlighted the importance for further work on this matter and need for multicenter validation. Full validation and standardization ","journal":"Allergy","year":2023,"id":324095,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":35,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9644,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2023-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1039965,"name":"Sanna Edelman","orcid":"0000-0002-3414-3187","position":1,"is_corresponding":false},{"id":1039966,"name":"Anna Nopp","orcid":"0000-0003-1389-8676","position":2,"is_corresponding":false},{"id":1039967,"name":"Christian Möbs","orcid":"0000-0002-5197-7669","position":3,"is_corresponding":false},{"id":1040783,"name":"Wolf‐Jochen Geilenkeuser","orcid":null,"position":4,"is_corresponding":false},{"id":770425,"name":"Edward F. Knol","orcid":"0000-0001-7368-9820","position":5,"is_corresponding":false},{"id":486894,"name":"Didier G. Ebo","orcid":"0000-0003-0672-7529","position":6,"is_corresponding":false},{"id":1039968,"name":"Christel Mertens","orcid":"0000-0003-2359-0771","position":7,"is_corresponding":false},{"id":465642,"name":"Mohamed H. Shamji","orcid":"0000-0003-3425-3463","position":8,"is_corresponding":false},{"id":249768,"name":"Alexandra F. Santos","orcid":"0000-0002-7805-1436","position":9,"is_corresponding":false},{"id":256892,"name":"Sarita U. 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