Evidence map›Paper›PMID 42533363›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2026

Gut microbial composition modulates endogenous food-specific CD4+ T cells in food allergy.

Alexa R Weingarden, Flannery S Dahlberg, Caroline N Broude, Xiandong Meng, Sunit Jain, Allison M Weakley, Ashley V Cabrera, Thamotharampillai Dileepan, Michael A Fischbach, Marc K Jenkins

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 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

5 · Who and what money

Authors and funding

10 authors.

Alexa R WeingardenCenter for Immunology, University of Minnesota Medical School, Minneapolis, MN, United States.
Flannery S DahlbergCenter for Immunology, University of Minnesota Medical School, Minneapolis, MN, United States.
Caroline N BroudeDepartment of Bioengineering, Stanford University, Stanford, CA, United States.
Xiandong MengMicrobiome Therapies Initiative (MITI), Stanford University, Stanford, CA, United States.
Sunit JainChan Zuckerberg Biohub, San Francisco, CA, United States.
Allison M WeakleyMicrobiome Therapies Initiative (MITI), Stanford University, Stanford, CA, United States.
Ashley V CabreraMicrobiome Therapies Initiative (MITI), Stanford University, Stanford, CA, United States.
Thamotharampillai DileepanCenter for Immunology, University of Minnesota Medical School, Minneapolis, MN, United States.
Michael A FischbachDepartment of Bioengineering, Stanford University, Stanford, CA, United States.
Marc K JenkinsCenter for Immunology, University of Minnesota Medical School, Minneapolis, MN, United States.ORCID 0000-0001-8009-7655

Funding

CD4+ T cell response to foodR01AI187164 · NIAID · UNIVERSITY OF MINNESOTA · PI Marc Kevin Jenkins · 2025 to 2026
$1.1M
30-parameter FACSymphony A3 flow cytometer for Shared Resource LabS10OD026831 · OD · STANFORD UNIVERSITY · PI NOLAN, GARRY P · 2019 to 2019
$510k
Life Science Research Foundation postdoctoral fellowship and Open PhilanthropyNational Institute of Allergy and Infectious Diseases (NIAID) R01AI187164NIAID NIH HHS R01 AI187164NIH HHS S10 OD026831
6 · The paper itself

Abstract

The growing food allergy epidemic is thought to be related to changing environmental factors, particularly changes in the gut microbiome. While prior work has demonstrated that food allergy can be modulated by gut microbes, little is known about how food allergen-specific CD4+ T cells are affected by gut microbial composition. Here, we report that food allergy severity differs between mice obtained from 2 different specific pathogen-free mouse vendors (Jackson Labs [Jax] and Taconic Biosciences [Tac]). Mice from Tac develop diarrhea and anaphylaxis after fewer allergen exposures than mice from Jax. Using food allergen peptide: MHCII tetramers, we also find that Tac mice have fewer allergen-specific regulatory T cells in the small intestine compared to mice from Jax with concomitant increase in allergen-specific Th2 cells. In addition, Tac mice have increased intestinal permeability. Increased food allergy severity, phenotype of allergen-specific T cells, and increased gut permeability were transferable to Jax animals via co-housing, which corresponded to a shift in Jax microbial communities towards those found in Tac mice. Our findings demonstrate that food allergen-specific Treg cells can be modulated by gut microbial community composition, which in turn is correlated to food allergy severity.

Indexed as

CD4-Positive T-LymphocytesFood HypersensitivityGastrointestinal MicrobiomeT-Lymphocytes, RegulatoryAllergensAnimalsDisease Models, AnimalFemaleMiceTh2 CellsAllergensfood allergyfood-specific T cellsgut microbiomeregulatory T cells

Identifiers

PMID42533363
PMCPMC13519244

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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.