Evidence mapPaperPMID 41304202Full record

ReviewMicroorganisms2025

Gut Microbiome and Immune System Crosstalk in Chronic Inflammatory Diseases: A Narrative Review of Mechanisms and Therapeutic Opportunities.

Jefferson J Feng, Nikhil R Maddirala, Ashley Saint Fleur, Fenfen Zhou, Di Yu, Feng Wei, Yongrong Zhang

Abstract readReview
In one paragraph

Review in Microorganisms, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  8. Article
  9. Review
  10. Review
  11. Frontiers in cellular and infection microbiology · 2026
    Article
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

7 authors.

Jefferson J FengDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.
Nikhil R MaddiralaDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.
Ashley Saint FleurDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.
Fenfen ZhouDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.
Di YuDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.ORCID 0000-0001-9354-8611
Feng WeiDepartment of Neural and Pain Sciences, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.
Yongrong ZhangDepartment of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD 21201, USA.ORCID 0000-0002-8594-4232

Funding

Characterization of neutralizing antitoxins and epitopes in Clostridium difficile patientsR01AI148270 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Hanping Feng · 2022 to 2024
$1.2M
Development of Oral Immunotherapy against Clostridioides difficile TransmissionR01AI190438 · UNIVERSITY OF MARYLAND BALTIMORE · 2025 to 2025
$512k
Development of probiotic-based and Clostridioides difficile-targeted therapeuticsR21AI183094 · UNIVERSITY OF SOUTH FLORIDA · 2025 to 2025
$190k
NIAID NIH HHS R01 AI148270NIAID NIH HHS R01 AI190438NIAID NIH HHS R21 AI183094
6 · The paper itself

Abstract

The gut microbiota, a complex community of trillions of microorganisms residing in the gastrointestinal tract, plays a vital role in maintaining host health and regulating a wide range of physiological functions. Advances in molecular biology have greatly expanded our understanding of the dynamic interactions between the gut microbiome and the immune system. Disruption of this microbial community, known as dysbiosis, can compromise epithelial barrier integrity, trigger aberrant immune activation, and lead to the production of proinflammatory metabolites. These changes are increasingly recognized as contributing factors in the pathogenesis of chronic inflammatory diseases. Emerging research highlights the gut microbiota as a key modulator of immune homeostasis, influencing both local and systemic inflammatory processes during the initiation and progression of these diseases. Understanding the mechanisms underlying gut microbiota-immune interactions will offer new avenues for therapeutic interventions. This review focuses on six representative chronic inflammatory diseases, including rheumatoid arthritis, inflammatory bowel disease, psoriasis, systemic lupus erythematosus, asthma, and vasculitis, all of which are characterized by dysregulated immune responses and persistent inflammation. Our goal is to synthesize the recent research on the role of gut microbiome in the pathogenesis of the diseases listed above and provide insights into the development of microbiota-based therapies, particularly fecal microbiota transplant, dietary modifications, prebiotic and probiotic interventions, for their treatment.

Indexed as

asthmachronic inflammationdysbiosisgut microbiomeimmune responseinflammatory bowel diseasepathogenesispsoriasisrheumatoid arthritissystemic lupus erythematosusvasculitis

Identifiers

PMID41304202
PMCPMC12654787

What Socratic holds

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Registered trials

None linked

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.