Evidence map›Paper›PMID 39340441›Full record

ArticleAllergy2025

Clinical utility analysis of the Hoxb8 mast cell activation test for the diagnosis of peanut allergy.

Noemi Bachmeier-Zbären, Alper Celik, Robin van Brummelen, Nadine Roos, Melanie Steinmann, Jennifer A Hoang, Xiaojun Yin, Christina M Ditlof, Lucy Duan, Julia E M Upton and 4 more

Abstract read
In one paragraph

Article in Allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Noemi Bachmeier-ZbärenDepartment of Rheumatology and Immunology, University Hospital Bern, Bern, Switzerland.
Alper CelikCentre for Computational Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.
Robin van BrummelenDepartment of Rheumatology and Immunology, University Hospital Bern, Bern, Switzerland.
Nadine RoosDepartment of Rheumatology and Immunology, University Hospital Bern, Bern, Switzerland.
Melanie SteinmannDepartment of Rheumatology and Immunology, University Hospital Bern, Bern, Switzerland.
Jennifer A HoangTranslational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0001-9264-1881
Xiaojun YinTranslational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.
Christina M DitlofDepartment of Immunology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Lucy DuanTranslational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.
Julia E M UptonDivision of Immunology and Allergy, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0001-5320-4232
Thomas KaufmannInstitute of Pharmacology, University of Bern, Bern, Switzerland.ORCID 0000-0001-9906-874X
Alexander EggelDepartment of Rheumatology and Immunology, University Hospital Bern, Bern, Switzerland.ORCID 0000-0001-8746-3339
Thomas EiweggerTranslational Medicine, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-2914-7829
MONAS working group

Funding

Food Allergy and Anaphylaxis Program at the Hospital for Sick ChildrenInnosuisse - Schweizerische Agentur für InnovationsförderungSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
6 · The paper itself

Abstract

backgroundPeanut allergy is among the most severe and common food allergies. The diagnosis has a significant impact on the quality of life for patients and their families. An effective management approach depends on accurate, safe, and easily implementable diagnostic methods. We previously developed a cell-based assay using Hoxb8 mast cells (Hoxb8 MCs) aimed at improving clinical allergy diagnosis. In this study, we assessed its diagnostic performance by measuring blinded sera from a prospectively enrolled and pre-validated peanut allergy cohort.

methodsHoxb8 MCs were passively sensitized with sera from peanut-allergic and peanut tolerant children and adolescents (n = 112). Degranulation of Hoxb8 MCs was quantified upon stimulation with dose-titrated peanut extract by means of flow cytometry, using CD107a as activation marker. The results from the Hoxb8 mast cell activation test (Hoxb8 MAT) were compared to established diagnostic assays such as the skin prick test (SPT), specific IgE (sIgE) levels, and the basophil activation test (BAT). Additionally, serum samples from BAT nonresponders were assessed with the Hoxb8 MAT.

resultsHoxb8 MAT displayed a robust dose-dependent activation to peanut extract, with a cutoff value of ≤5.2% CD107a positive cells. The diagnostic accuracy was highest at allergen concentrations ≥100 ng/mL, with an area under the receiver operating characteristic curve (AUROC) of 0.97, 93% sensitivity, and 96% specificity, outperforming traditional SPT and sIgE tests. When compared to BAT, Hoxb8 MAT exhibited comparable diagnostic efficacy. Moreover, sera from BAT nonresponders were accurately classified into allergics and nonallergics by the Hoxb8 MAT.

conclusionsThe Hoxb8 MAT demonstrated a very good diagnostic precision in patients prospectively assessed for peanut allergy comparable to the fresh whole blood-based BAT. Additionally, it demonstrated its value for accurate classification of BAT nonresponders into allergic and nonallergic individuals. Further investigations into its utility in the routine clinical setting are warranted.

Indexed as

Homeodomain ProteinsMast CellsPeanut HypersensitivityAdolescentAllergensCell DegranulationChildChild, PreschoolFemaleHumansImmunoglobulin EInfantMaleSensitivity and SpecificitySkin TestsAllergensHomeodomain ProteinsImmunoglobulin Ebasophil activation testHoxb8 mast cell activation testoral food challengepeanut allergy diagnosisspecific IgE

Identifiers

PMID39340441
PMCPMC11724244

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.