Evidence map›Paper›PMID 41647192›Full record

ArticleFrontiers in allergy2025

MRGPRX2-expressing mast cells are increased in the GI tract of individuals with active inflammatory bowel disease and hereditary α-tryptasemia.

Michelle Galeas-Pena, Jonathan J Lyons, Dhana Llivichuzhca-Loja, Steve Everman, Ghina Yaghi, Katelyn White, Sangita Sutradhar, Tanya O Robinson, Anna H Owings, Neha S Dhaliwal and 4 more

Abstract read
In one paragraph

Article in Frontiers in allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Michelle Galeas-PenaSection of Gastroenterology, Department of Medicine, Tulane University School of Medicine, New Orleans, LA, United States.
Jonathan J LyonsDivision of Allergy & Immunology, Department of Medicine, University of California San Diego, La Jolla, CA, United States.
Dhana Llivichuzhca-LojaDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, United States.
Steve EvermanDivision of Digestive Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, MS, United States.
Ghina YaghiSection of Gastroenterology, Department of Medicine, Tulane University School of Medicine, New Orleans, LA, United States.
Katelyn WhiteSection of Gastroenterology, Department of Medicine, Tulane University School of Medicine, New Orleans, LA, United States.
Sangita SutradharDepartment of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Tanya O RobinsonDivision of Digestive Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, MS, United States.
Anna H OwingsDivision of Digestive Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, MS, United States.
Neha S DhaliwalDivision of Digestive Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, MS, United States.
Alexander CarlyeDivision of Digestive Diseases, Department of Medicine, University of Mississippi Medical Center, Jackson, MS, United States.
Liza KonnikovaDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, United States.
Hydar AliDepartment of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Sarah C GloverSection of Gastroenterology, Department of Medicine, Tulane University School of Medicine, New Orleans, LA, United States.

Funding

TPSAB1-derived tryptases promote myeloproliferation and anaphylaxisR00AI138586 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jonathan Lyons · 2024 to 2026
$2.3M
Repurposing Pharmacological Agents for Inherited Mast CellDisorders of the GutR21TR002639 · NCATS · YALE UNIVERSITY · PI GLOVER, SARAH C, HAMILTON, MATTHEW J · 2019 to 2020
$535k
Mast Cell G-protein Coupled Receptors in Immune Modulation of colitisR21AI190597 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALI, HYDAR · 2025 to 2025
$447k
NCATS NIH HHS R21 TR002639NIAID NIH HHS R00 AI138586NIAID NIH HHS R21 AI190597
6 · The paper itself

Abstract

Introduction: Hereditary α-tryptasemia (HαT), defined by increased Methods: We genotyped 854 biobanked IBD samples to identify individuals with HαT. Spatial transcriptomic analysis was performed on descending colon tissue from individuals with HαT ( Results: Across complementary platforms, HαT was associated with increased gastrointestinal mast cell abundance and elevated expression of mast cell activation markers, including CD203c, LAMP-1, and SIGLEC8. Both spatial transcriptomics and ddPCR demonstrated significantly increased Discussion: These findings suggest that enhanced MRGPRX2 expression and mast cell activation may contribute to gastrointestinal symptoms in individuals with HαT, particularly in the setting of IBD. As interest in precision immunogenetics grows, defining mast cell phenotypes linked to α-tryptase copy number may help refine diagnostic evaluation and identify patients who could benefit from emerging mast cell-targeted therapeutic strategies in the context of IBD.

Indexed as

gastrointestinal tracthereditary alpha-tryptasemiainflammatory bowel diseasemass cytometrymast cellsMRGPRX2SIGLEC8

Identifiers

PMID41647192
PMCPMC12868144

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.