Evidence map›Paper›PMID 33772805›Full record

ArticleAllergy2021

CytoBas: Precision component-resolved diagnostics for allergy using flow cytometric staining of basophils with recombinant allergen tetramers.

Craig I McKenzie, Nirupama Varese, Pei M Aui, Bruce D Wines, Philip Mark Hogarth, Francis Thien, Mark Hew, Jennifer M Rolland, Robyn E O'Hehir, Menno C van Zelm

Open access · hybridAbstract read
In one paragraph

Article in Allergy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 23% of its field
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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Craig I McKenzieDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-7070-620X
Nirupama VareseDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-9074-3710
Pei M AuiDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-2314-9989
Bruce D WinesDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-4108-375X
Philip Mark HogarthDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-0360-7890
Francis ThienRespiratory Medicine, Eastern Health, Box Hill and Monash University, Melbourne, VIC, Australia.ORCID 0000-0003-0925-6566
Mark HewSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-7498-0000
Jennifer M RollandDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-7891-983X
Robyn E O'HehirDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-3489-7595
Menno C van ZelmDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.ORCID 0000-0003-4161-1919
Monash University · AUAlfred Health · AUBurnet Institute · AUEastern Health · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiagnostic tests for allergy rely on detecting allergen-specific IgE. Component-resolved diagnostics incorporate multiple defined allergen components to improve the quality of diagnosis and patient care.

objectiveTo develop a new approach for determining sensitization to specific allergen components that utilizes fluorescent protein tetramers for direct staining of IgE on blood basophils by flow cytometry.

methodsRecombinant forms of Lol p 1 and Lol p 5 proteins from ryegrass pollen (RGP) and Api m 1 from honeybee venom (BV) were produced, biotinylated, and tetramerized with streptavidin-fluorochrome conjugates. Blood samples from 50 RGP-allergic, 41 BV-allergic, and 26 controls were incubated with fluorescent protein tetramers for flow cytometric evaluation of basophil allergen binding and activation.

resultsAllergen tetramers bound to and activated basophils from relevant allergic patients but not controls. Direct fluorescence staining of Api m 1 and Lol p 1 tetramers had greater positive predictive values than basophil activation for BV and RGP allergy, respectively, as defined with receiver operator characteristics (ROC) curves. Staining intensities of allergen tetramers correlated with allergen-specific IgE levels in serum. Inclusion of multiple allergens coupled with distinct fluorochromes in a single-tube assay enabled rapid detection of sensitization to both Lol p 1 and Lol p 5 in RGP-allergic patients and discriminated between controls, BV-allergic, and RGP-allergic patients.

conclusionOur novel flow cytometric assay, termed CytoBas, enables rapid and reliable detection of clinically relevant allergic sensitization. The intensity of fluorescent allergen tetramer staining of basophils has a high positive predictive value for disease, and the assay can be multiplexed for a component-resolved and differential diagnostic test for allergy.

Indexed as

BasophilsHypersensitivityAllergensFlow CytometryHumansStaining and LabelingAllergensallergen tetramersbasophilscomponent-resolved diagnosticsflow cytometrysurface IgE

Identifiers

PMID33772805
PMCPMC8518718
OpenAlexW3111255997

What OpenQuestion holds

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LicenceCC BY-NC
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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.