Evidence map›Paper›PMID 41888808›Full record

ArticleRespiratory research2026

Ex vivo allergen specific type 2 immune responses in house dust mite-driven acute airway inflammation in mice depend on allergen extract characteristics.

Roos E M Verstegen, Suzan Thijssen, Atanaska I Kostadinova, Johan Garssen, Gert Folkerts, Rudi W Hendriks, Linette E M Willemsen

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

7 authors.

Roos E M VerstegenDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, the Netherlands. r.e.m.verstegen@uu.nl.
Suzan ThijssenDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, the Netherlands.
Atanaska I KostadinovaDanone Global Research & Innovation Centre, Utrecht, the Netherlands.
Johan GarssenDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, the Netherlands.
Gert FolkertsDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, the Netherlands.
Rudi W HendriksDepartment of Pulmonary Medicine, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, the Netherlands.
Linette E M WillemsenDivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, the Netherlands. l.e.m.willemsen@uu.nl.

Funding

Health~Holland 10.1.19.001Longfonds 10.1.19.001
6 · The paper itself

Abstract

House dust mite (HDM) is frequently used in animal models of allergic airway diseases. HDM extracts differ in allergen concentration and endotoxin contamination, requiring model optimalization for each batch. This study aimed to refine and validate our murine model of HDM-driven acute allergic airway inflammation with a new batch of HDM extract and comparing different administration doses.We evaluated three HDM extracts, HDM1 (old batch), HDM2 and HDM3, containing varying Der p1 concentrations (33.7, 71.4 and 9.0 mg/g protein) and endotoxin levels (94.8, 53.9 and 24.7 EU/g protein). Male BALB/c mice were intranasally sensitized (day 0) with 1 µg (HDMlow) or 5 µg (HDMhigh), and challenged (day 7–11) with 10 µg (HDMlow) or 15 µg (HDMhigh) of the same HDM extract. Bronchoalveolar lavage fluid (BALF), lung tissue and serum were collected on day 14.High doses of all extracts significantly increased BALF total cell influx, including eosinophils and lymphocytes, and elevated lung Th2 and CD69 + Th2 cell frequencies. Eosinophils and lymphocytes induction varied across extracts (6–17 × 104 and 3–8 × 104 cells respectively). HDM3high tended (p < 0.1) to increase serum HDM-specific IgE. Upon ex-vivo HDM-restimulation of lung cells comparing HDM3 high with HDM2 high, only cells of HDM3high-treated mice showed increased IL-5 and IL-13 production.Overall, the high dose protocol most effectively induced HDM-driven acute allergic airway inflammation, based on BALF eosinophil and lymphocyte influx. Even though having low Der p1 and endotoxin levels, only HDM3high enhanced cytokine production upon ex-vivo HDM-restimulation, indicating the value of this functional assay to discriminate between HDM batches.

Indexed as

AllergensAntigens, DermatophagoidesDust Mite AllergyLungPyroglyphidaeTh2 CellsAnimalsBronchoalveolar Lavage FluidCytokinesDisease Models, AnimalImmunoglobulin EMaleMiceMice, Inbred BALB CAllergensAntigens, DermatophagoidesCytokinesImmunoglobulin EAllergic airway inflammationAnimal modelAsthmaHouse dust mite

Identifiers

PMID41888808
PMCPMC13019866

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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.