Evidence map›Paper›PMID 41998808›Full record

ArticleAllergy2026

Biphasic Effects on Allergen-Specific Type 2 Memory B Cells Over 18 Months Sublingual Immunotherapy for House Dust Mite Allergy.

Lin Hsin, Simone Reinwald, Anouk von Borstel, Pei Mun Aui, Kirsten Deckert, P Mark Hogarth, Laurent Mascarell, Mark Hew, Robyn E O'Hehir, Menno C van Zelm

Abstract read
In one paragraph

Article in Allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lin HsinDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-7082-4011
Simone ReinwaldDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-9001-9367
Anouk von BorstelDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.ORCID https://orcid.org/0000-0002-3605-7936
Pei Mun AuiDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-2314-9989
Kirsten DeckertAllergy, Asthma and Clinical Immunology, Alfred Health, Melbourne, Victoria, Australia.
P Mark HogarthDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-0360-7890
Laurent MascarellInnovation & Science Department, Stallergenes Greer, Antony, France.ORCID https://orcid.org/0000-0001-7199-0345
Mark HewAllergy, Asthma and Clinical Immunology, Alfred Health, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-7498-0000
Robyn E O'HehirDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-3489-7595
Menno C van ZelmDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-4161-1919

Funding

National Health and Medical Research Council 2000773
6 · The paper itself

Abstract

backgroundType 2 memory B cells (Bmem) are the reservoir of pathogenic IgE in allergies. Allergen immunotherapy (AIT) can change the course of disease, but if it involves reprogramming of allergen-reactive Bmem remains unknown. Here, we examine how AIT affects allergen-specific Bmem in house dust mite (HDM) allergic patients.

methodsHDM allergic patients were longitudinally evaluated over 18 months with or without sublingual HDM-AIT. Visual analog scores, lung function tests, medication scores, serum IgE, and flowcytometric analysis of Der p 1 and Der p 2-specific Type 2 Bmem were performed at t = 0, 4, 12, and 18 months.

resultsPatients on HDM-AIT showed clinical improvement over 18 months with reduced intake of other medications and increases in specific serum IgE, IgG2, and IgG4. Allergen-specific Bmem and the proportions of Type 2 Bmem therein became more abundant at 4 and 12 months and showed upregulation of CD29 and IgG4. At 18 months, the Type 2 Bmem proportions were reduced.

conclusionA biphasic Bmem response with early phenotypic changes followed by loss of the Type 2 state was observed during 18 months of AIT. As durable unresponsiveness takes 18 months of AIT, deletion of Type 2 Bmem is likely an important step in disease attenuation. Interventions that expedite this outcome may be beneficial in driving remission.

Indexed as

Antigens, DermatophagoidesB-LymphocytesDermatophagoides pteronyssinusDust Mite AllergyImmunologic MemoryMemory B CellsSublingual ImmunotherapyAllergensAnimalsArthropod ProteinsFemaleHumansImmunoglobulin EImmunoglobulin GMaleTreatment OutcomeAllergensAntigens, DermatophagoidesArthropod ProteinsImmunoglobulin EImmunoglobulin Gallergen immunotherapyallergic rhinitis (AR)atopic asthmahouse dust mitetype 2 memory B cells

Identifiers

PMID41998808
PMCPMC13256270

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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.