Evidence map›Paper›PMID 42154289›Full record

ArticleLung2026

The Platelet/Megakaryocyte Axis is Necessary for Allergic Sensitisation and Inflammatory Responses to House Dust Mite in the Lung.

Anna Chalidou, Katie-Marie Case, Carl Hobbs, Clive P Page, Simon C Pitchford

Abstract read
In one paragraph

Article in Lung, 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
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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

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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

5 authors.

Anna ChalidouPulmonary Pharmacology Unit, Institute of Pharmaceutical Science, King's College London, Room 5.43 Franklin Wilkins Building, Waterloo Campus, London, SE9 1NH, UK.
Katie-Marie CasePulmonary Pharmacology Unit, Institute of Pharmaceutical Science, King's College London, Room 5.43 Franklin Wilkins Building, Waterloo Campus, London, SE9 1NH, UK.
Carl HobbsWolfson SPaRC (Sensory, Pain and Regeneration Centre), Institute of Psychiatry, Psychology & Neuroscience, King's College London, Guy's Campus, London, SE1 1UL, UK.
Clive P PagePulmonary Pharmacology Unit, Institute of Pharmaceutical Science, King's College London, Room 5.43 Franklin Wilkins Building, Waterloo Campus, London, SE9 1NH, UK.
Simon C PitchfordPulmonary Pharmacology Unit, Institute of Pharmaceutical Science, King's College London, Room 5.43 Franklin Wilkins Building, Waterloo Campus, London, SE9 1NH, UK. Simon.pitchford@kcl.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence demonstrates that megakaryocytes (MKs) possess antigen processing and presentation properties. We investigated whether sensitisation to house dust mite (HDM) extract and the establishment of allergic pulmonary inflammation was dependent on the presence of platelets, and whether the allergic phenotype had an effect on antigen-presenting marker expression on MKs and platelets.

methodsBalb/c mice were administered anti-GPIbα antibody or an isotype control during days 0, 2, and 4 to temporarily deplete circulating platelets during initial sensitization to allergen (HDM extract) via an extended intranasal administration on days 0-4, 7-11, and 13. Bronchoalveolar lavage was undertaken, along with blood samples, and lung histology to quantify leukocyte recruitment, Th2 cytokine analysis, and lung platelet deposition. Lung MKs, bone marrow MKs, and circulating platelets were analysed from both allergen-sensitized and non-sensitized mice for the expression of MHC class I, MHC class II, FcεRIα, and CD40.

resultsTemporary platelet depletion limited to the initial phase of allergen sensitization inhibited the development of the allergic pulmonary phenotype to HDM as demonstrated by reduced eosinophil recruitment, IgE titre, IL-4 and IL-13 expression. Lung-resident MKs demonstrated higher expression of MHC class II and FcεRIα when compared to bone marrow (BM) MKs on establishment of an allergic phenotype, suggesting the administration of HDM specifically affected the immune-phenotype of the lung niche of MKs rather than the bone marrow niche, or systemic effects on circulating platelets. Platelets within the lung were observed to have increased co-localisation frequency with CD11c-positive antigen-presenting cells (APCs), but not CD4-positive T cells, suggesting that platelet activation may occur during the initial steps of allergen sensitisation.

conclusionThe platelet/MK axis is a requirement for sensitisation to HDM. An allergic phenotype selectively influences the immune signature of MKs in the lung.

Indexed as

Blood PlateletsDust Mite AllergyLungMegakaryocytesPneumoniaPyroglyphidaeAnimalsBronchoalveolar Lavage FluidDisease Models, AnimalFemaleImmunoglobulin EInterleukin-13Interleukin-4MiceMice, Inbred BALB CPhenotypeFcepsilonRIalpha protein, mouseImmunoglobulin EInterleukin-13Interleukin-4Receptors, IgEAntigen-presenting cellsHDMIgEIL-13IL-4MegakaryocytesMHC Class IIPlateletsSensitisation

Identifiers

PMID42154289
PMCPMC13186874

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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.