Evidence map›Paper›PMID 42118094›Full record

ArticleJournal of leukocyte biology2026

Three-dimensional modeling of sensory nerve architecture and eosinophil and mast cell interactions in eosinophilic gastrointestinal disease.

Ari M Levine, Megan Koch, Julius Herzog, Juraj Kabat, Margery Smelkinson, Armando Arroyo-Mejias, Mian B Khalid, Disha Sharma, Alla Turshudzhyan, Sheila Kumar and 3 more

Abstract read
In one paragraph

Article in Journal of leukocyte 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

13 authors.

Ari M LevineHuman Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.
Megan KochHuman Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0002-4911-5998
Julius HerzogVector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 12735 Twinbrook Parkway, Bethesda, MD 20852, United States.
Juraj KabatBiological Imaging Section, Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, 9000 Rockville Pike, MD20892, United States.ORCID 0000-0001-8636-542X
Margery SmelkinsonBiological Imaging Section, Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, 9000 Rockville Pike, MD20892, United States.ORCID 0000-0001-7777-5574
Armando Arroyo-MejiasLymphocyte Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0002-0835-911X
Mian B KhalidNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.
Disha SharmaNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.
Alla TurshudzhyanNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0001-6867-7569
Sheila KumarNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0003-0549-7768
Paneez KhouryHuman Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0003-1800-0079
Amy D KlionHuman Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0002-4986-5326
Gregory M ConstantineHuman Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD20892, United States.ORCID 0000-0001-5379-9475

Funding

NIHNIH HHSU.S. Department of Health and Human ServicesU.S. government
6 · The paper itself

Abstract

Increased sensory nerve density has been described in type 2 inflammatory conditions and is linked to eosinophil and mast cell infiltration and neuropathic pain. To examine these relationships in eosinophilic gastrointestinal diseases, we developed a protocol using Ce3D (clearing-enhanced 3D) tissue clearing to evaluate mucosal gastrointestinal (GI) nerve remodeling and interactions with eosinophils and mast cells in whole-mount GI biopsies. Human gastric and esophageal biopsies were processed for 3-dimensional imaging. Tissues were fixed, permeabilized, and immunolabeled for mucosal nerves (Protein Gene Product 9.5), sensory neurons (substance P), eosinophils (eosinophil peroxidase), mast cells (tryptase), and epithelial cells (pan-cytokeratin). Vacuum-microwave-assisted staining was employed to enhance antibody penetration and protocol efficiency. Samples were cleared with Ce3D and imaged using confocal microscopy. Machine learning-enhanced quantitative analysis and modeling of nerve morphology and cellular interactions, including nerve length, branching, and spatial relationships between eosinophils, mast cells, and sensory neurons were performed. We established a 3-dimensional imaging method for whole-mount GI biopsies to characterize nerve architecture and eosinophil and mast cell interactions in the human esophagus and stomach. This approach enables high resolution and volumetric analyses and can be modified to assess other spatial neuroimmune interactions in human GI mucosal biopsies.

Indexed as

Cell CommunicationEnteritisEosinophiliaEosinophilsGastritisImaging, Three-DimensionalMast CellsSensory Receptor CellsEsophagusHumans3D imagingenteric nervous systemeosinophileosinophilic gastrointestinal diseaseneuroimmune interactions

Identifiers

PMID42118094
PMCPMC13196879

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.