Evidence map›Paper›PMID 42327263›Full record

ArticlebioRxiv : the preprint server for biology2026

Eosinophil-epithelial interactions mediate protective intestinal remodeling during food allergy.

Patrick W Darcy, Vitoria M Olyntho, Albana Kodra, Zachary Kerner, Maria C C Canesso, Sandra Nakandakari-Higa, Gabriel Victora, Daniel Mucida

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

8 authors.

Patrick W DarcyLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-7696-3212
Vitoria M OlynthoLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Albana KodraLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Zachary KernerLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Maria C C CanessoLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.
Sandra Nakandakari-HigaLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY 10065, USA.
Gabriel VictoraLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY 10065, USA.
Daniel MucidaLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY 10065, USA.ORCID 0000-0002-0000-0452

Funding

Transgenic CoreP01AI179273 · NIAID · FOOD ALLERGY SCIENCE INITIATIVE, INC. · PI BRADFORD B LOWELL · 2024 to 2026
$9.4M
INTESTINAL REGULATION OF ThPOK EXPRESSION AND CD4 HELPER T CELL FUNCTIONR01DK093674 · NIDDK · ROCKEFELLER UNIVERSITY · PI Daniel S Mucida · 2013 to 2026
$7.0M
Intestinal surveillance by intraepithelial lymphocytesR01DK113375 · NIDDK · ROCKEFELLER UNIVERSITY · PI Semir Beyaz, Daniel S Mucida · 2017 to 2026
$5.5M
B cell clonal selection in gut-associated germinal centersR01AI157137 · NIAID · ROCKEFELLER UNIVERSITY · PI Daniel S Mucida, Gabriel D Victora · 2020 to 2026
$4.8M
NIAID NIH HHS P01 AI179273NIAID NIH HHS R01 AI157137NIDDK NIH HHS R01 DK093674NIDDK NIH HHS R01 DK113375
6 · The paper itself

Abstract

Food allergies are associated with progressive gastrointestinal symptoms driven by exacerbated mucosal type-2 immunity. Here, we investigated whether cellular interactions between the gut epithelium and innate immune cells regulate the severity of allergic symptoms in mice. Using the BALB/c OVA-alum food allergy model, we observed that repeated oral allergen challenges remodel the gut epithelium, expanding tuft cells, while shifting the intestinal stem cell niche toward a fetal-like repair state. Using uLIPSTIC, we systematically characterized in vivo immune-epithelial interactions and found that eosinophils and mast cells directly interact with intestinal epithelial cells (iECs) in an allergen challenge-dependent manner. Epithelial subset-specific uLIPSTIC provided further resolution and revealed that eosinophils and mast cells contact enteroendocrine cells and Paneth cells in a regionally compartmentalized manner. Allergic challenge was associated with rapid eosinophil migration towards the crypts and modulation of iEC differentiation. Depletion of eosinophils using two independent approaches reversed key markers of food allergy-associated epithelial remodeling, while exacerbating allergic diarrhea and mortality from anaphylactic shock. These findings establish eosinophils as orchestrators of protective epithelial remodeling in food allergies.

Identifiers

PMID42327263
PMCPMC13278080

What OpenQuestion holds

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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.