Evidence map›Paper›PMID 42396442›Full record

ReviewFrontiers in immunology2026

Gut barrier-microbiota crosstalk in sepsis: from pathogenesis to potential therapies.

Lingshuai Meng, Yingjie Liu, Nana Wang, Tiegang Li, Yu Wang, Mandi Li

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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

6 authors.

Lingshuai MengDepartment of Emergency Medicine, Shengjing Hospital of China Medical University, Shenyang, China.
Yingjie LiuDepartment of Emergency Medicine, Shengjing Hospital of China Medical University, Shenyang, China.
Nana WangDepartment of Clinical Trial Unit, Shengjing Hospital of China Medical University, Shenyang, China.
Tiegang LiDepartment of Emergency Medicine, Shengjing Hospital of China Medical University, Shenyang, China.
Yu WangDepartment of Emergency Medicine, Shengjing Hospital of China Medical University, Shenyang, China.
Mandi LiSchool of Mechanical Engineering, Shenyang Jianzhu University, Shenyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a systemic inflammatory response syndrome triggered by infection, frequently complicated by severe organ dysfunction and high mortality rates. Recent studies of intestinal epithelial function and the gut microbiota have highlighted their pivotal roles in the pathogenesis of sepsis. However, the precise mechanisms governing the interaction between the intestinal epithelium and gut microbiota, and how this interaction drives sepsis progression, still need to be elucidated. In this review, the functions of the intestinal epithelial barrier are first outlined, and the clinical significance of its altered permeability during sepsis is highlighted. Then, the physiological roles of the gut microbiota are further explored, detailing how dysbiosis and microbial metabolites influence disease progression and trigger both localized and systemic immune responses. Based on this, a logical framework for gut-originated systemic inflammation is proposed, and the potential adverse effects of current clinical supportive therapies on intestinal integrity are further discussed. Finally, the emerging sepsis treatment strategies that target gut function are summarized, aiming to provide novel insights and therapeutic directions for clinical practice.

Indexed as

Gastrointestinal MicrobiomeIntestinal MucosaSepsisAnimalsDysbiosisHumansIntestinal Barrier Functiongut microbiotainflammatory responseintestinal epithelial barriermedical treatmentsepsis

Identifiers

PMID42396442
PMCPMC13322907

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.