Evidence map›Paper›PMID 41207641›Full record

ArticleThe Journal of allergy and clinical immunology2026

Basophils activate oncostatin M receptor-expressing vagal sensory neurons.

Jo-Chiao Wang, Kicheon Park, Anais Roger, Amin Reza Nikpoor, Theo Crosson, Hoon James Sunwoo, Eva Kaufmann, Moutih Rafei, Eric H Chang, Sebastien Talbot

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Jo-Chiao WangDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, Quebec, Canada.
Kicheon ParkInstitute for Bioelectronic Medicine, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY.
Anais RogerDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.
Amin Reza NikpoorDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.
Theo CrossonDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, Quebec, Canada.
Hoon James SunwooDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.
Eva KaufmannDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada; Meakins-Christie Laboratories, RI-MUHC, and Faculty of Dental Medicine and Oral Health Sciences, McGill University, Montreal, Quebec, Canada.
Moutih RafeiDepartment of Pharmacology and Physiology, Université de Montréal, Montreal, Quebec, Canada.
Eric H ChangInstitute for Bioelectronic Medicine, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY.
Sebastien TalbotDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. Electronic address: sebas.talbot@gmail.com.

Funding

Intra-tumoral neurons contribute to head and neck cancer painR01DE032712 · NIDCR · SANFORD RESEARCH/USD · PI Paola Drapkin Vermeer · 2023 to 2026
$1.8M
Encoding of inflammatory mediators by vagal sensory neuronsR01GM143362 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI CHANG, ERIC HAU-YUN · 2021 to 2024
$1.6M
NIDCR NIH HHS R01 DE032712NIGMS NIH HHS R01 GM143362
6 · The paper itself

Abstract

backgroundVagal sensory neurons (VSNs) relay signals from internal organs to the brainstem via the vagus nerve. Published transcriptomic data sets suggest that VSNs express Mas-related G protein-coupled receptor family member D and oncostatin M (OSM) receptor, markers also found in dorsal root ganglia-resident pruriceptor neurons. However, the cellular source of OSM and its potential interactions with VSNs remain unknown.

objectiveWe sought to validate the expression of pruritogen receptors on VSNs, identify basophils as a source of OSM, and determine how OSM modulates VSN activity.

methodsPruritogen receptor expression on VSNs was validated by immunofluorescence staining, and VSN responses to pruritogens were assessed using in vitro and in vivo calcium imaging. Mouse models of allergic airway inflammation, fluorescence-activated cell sorting, quantitative PCR, and ELISA were used to evaluate OSM expression and production by lung basophils.

resultsImmunofluorescence and quantitative PCR confirmed that airway-innervating VSNs express OSM receptor and that lung basophils are enriched for Osm transcripts. Lung-resident basophils produced OSM following FcεRIα engagement, with production further enhanced after sensitization to house dust mite (Dermatophagoides pteronyssinus) or the fungal allergen Alternaria alternata. In vitro and in vivo calcium imaging revealed that OSM sensitizes multiple populations of VSNs.

conclusionsThese findings identify a novel mechanism of communication between basophils and VSNs during type I hypersensitivity reactions, such as those occurring in allergic asthma.

Indexed as

BasophilsOncostatin M Receptor beta SubunitSensory Receptor CellsVagus NerveAnimalsDisease Models, AnimalFemaleLungMiceMice, Inbred C57BLOncostatin MOncostatin MOncostatin M Receptor beta SubunitallergyasthmabasophilsNeuroimmunologynociceptor neuronsOSM

Identifiers

PMID41207641
PMCPMC13384724

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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.