Evidence map›Paper›PMID 38177249›Full record

ArticlePediatric research2024

Novel Bacteroides Vulgatus strain protects against gluten-induced break of human celiac gut epithelial homeostasis: a pre-clinical proof-of-concept study.

Tina Tran, Stefania Senger, Mariella Baldassarre, Rachel A Brosnan, Fernanda Cristofori, Marco Crocco, Stefania De Santis, Luca Elli, Christina S Faherty, Ruggero Francavilla and 16 more

Open access · hybridAbstract read
In one paragraph

Article in Pediatric research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.1field-weighted citation impact, top 5% of its field
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

9 citing papers in PubMed, 11 citations in OpenAlex.

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  5. Role of phase-variable Mfa1 fimbriae ofGut microbes reports · 2025
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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

26 authors at 17 institutions in 3 countries.

Tina TranMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Stefania SengerCenter for Scientific Review, National Institutes of Health, Bethesda, MD, USA.
Mariella BaldassarreNICU, University of Bari, Bari, Italy.
Rachel A BrosnanMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Fernanda CristoforiPediatric Unit "Bruno Trambusti", Osp Pediatrico Giovanni XXIII, University of Bari, Bari, Italy.
Marco CroccoDepartment of Pediatrics, IRCCS Ospedale Giannina Gaslini, Genova, Italy.
Stefania De SantisDigestive Health Research Institute, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Luca ElliCeliac Disease Referral Center, Ospedale Maggiore Policlinico, Milan, Italy.
Christina S FahertyMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Ruggero FrancavillaPediatric Unit "Bruno Trambusti", Osp Pediatrico Giovanni XXIII, University of Bari, Bari, Italy.
Isabella Goodchild-MichelmanMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Victoria A KenyonMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Maureen M LeonardMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Rosiane S LimaMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Federica MalerbaDepartment of Pediatrics, IRCCS Ospedale Giannina Gaslini, Genova, Italy.
Monica MontuoriPediatric Gastroenterology Unit, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.
Annalisa MorelliPediatric Training Program, University of Salerno School of Medicine, Salerno, Italy.
Lorenzo NorsaPediatric Hepatology Gastroenterology and Transplant Unit, Ospedale Papa Giovanni XXIII Bergamo, Bergamo, Italy.
Tiziana PassaroCeliac Disease Referral Center, "San Giovanni di Dio e Ruggi d'Aragona" University Hospital, Pole of Cava de' Tirreni, Salerno, Italy.
Pasqua PiemonteseNICU, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
James C ReedMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Naire SansottaPediatric Hepatology Gastroenterology and Transplant Unit, Ospedale Papa Giovanni XXIII Bergamo, Bergamo, Italy.
Francesco ValituttiPediatric Gastroenterology and Liver Unit, Santobono-Pausilipon Children's Hospital, Naples, Italy.
Ali R ZomorrodiMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Alessio FasanoMucosal Immunology and Biology Research Center, Division of Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital; Department of Pediatrics, Harvard Medical School, Boston, MA, USA. afasano@mgh.harvard.edu.
CDGEMM Team
Harvard University · USEuropean Biomedical Research Institute of Salerno · ITMarche Polytechnic University · ITIstituto Giannina Gaslini · ITMassachusetts General Hospital · USUniversity of Milan · ITOspedale Papa Giovanni XXIII · ITOspedale Pediatrico Giovanni XXIII · ITPoliclinico Umberto I · ITBambino Gesù Children's Hospital · ITNational Institutes of Health · USOspedale Maggiore · ITOspedali Riuniti San Giovanni di Dio e Ruggi d'Aragona · ITUniversity of Bari Aldo Moro · ITUniversity of Bologna · ITUniversity of Salerno · ITUniversity School · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Elizabeth Austen Lawson, Takara Leah Stanley · 1994 to 2026
$31.6M
The Celiac Disease Genomic, Environmental, Microbiome, and Metabolomic (CD-GEMM) Prospective Cohort StudyR56AI169645 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI FASANO, ALESSIO · 2023 to 2023
$823k
The Celiac Disease Genome, Environment, Microbiome, and Metabolome (CD-GEMM) prospective cohort studyR56AI156711 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI FASANO, ALESSIO · 2021 to 2021
$410k
NIAID NIH HHS R56 AI156711NIAID NIH HHS R56 AI169645NIDDK NIH HHS P30 DK040561NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

BACKGROUND AND

aimsWe have identified a decreased abundance of microbial species known to have a potential anti-inflammatory, protective effect in subjects that developed Celiac Disease (CeD) compared to those who did not. We aim to confirm the potential protective role of one of these species, namely Bacteroides vulgatus, and to mechanistically establish the effect of bacterial bioproducts on gluten-dependent changes on human gut epithelial functions.

methodsWe identified, isolated, cultivated, and sequenced a unique novel strain (20220303-A2) of B. vulgatus found only in control subjects. Using a human gut organoid system developed from pre-celiac patients, we monitored epithelial phenotype and innate immune cytokines at baseline, after exposure to gliadin, or gliadin plus B. vulgatus cell free supernatant (CFS).

resultsFollowing gliadin exposure, we observed increases in epithelial cell death, epithelial monolayer permeability, and secretion of pro-inflammatory cytokines. These effects were mitigated upon exposure to B. vulgatus 20220303-A2 CFS, which had matched phenotype gene product mutations. These protective effects were mediated by epigenetic reprogramming of the organoids treated with B. vulgatus CFS.

conclusionsWe identified a unique strain of B. vulgatus that may exert a beneficial role by protecting CeD epithelium against a gluten-induced break of epithelial tolerance through miRNA reprogramming. IMPACT: Gut dysbiosis precedes the onset of celiac disease in genetically at-risk infants. This dysbiosis is characterized by the loss of protective bacterial strains in those children who will go on to develop celiac disease. The paper reports the mechanism by which one of these protective strains, B. vulgatus, ameliorates the gluten-induced break of gut epithelial homeostasis by epigenetically re-programming the target intestinal epithelium involving pathways controlling permeability, immune response, and cell turnover.

Indexed as

BacteroidesCeliac DiseaseGastrointestinal MicrobiomeGlutensIntestinal MucosaCytokinesEpithelial CellsGliadinHomeostasisHumansOrganoidsProof of Concept StudyCytokinesGliadinGlutens

Identifiers

PMID38177249
PMCPMC11035120
OpenAlexW4390579674

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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.