Evidence map›Paper›PMID 40691287›Full record

ArticlePediatric research2026

Murine intestinal epithelial cells and lymphocytes undergo contrasting inflammatory shifts during gastrointestinal development.

Thomas C Wiemers, Jan Riedel, Niklas Dressler, Xiaoyan Feng, Nicole Peukert, Martin Lacher, Steffi Mayer

Abstract read
In one paragraph

Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

7 authors.

Thomas C Wiemers *Department for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany. thomas.wiemers@medizin.uni-leipzig.de.ORCID http://orcid.org/0009-0000-2053-3857
Jan Riedel *Department for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.
Niklas DresslerDepartment for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.
Xiaoyan FengDepartment for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.
Nicole PeukertDepartment for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.
Martin LacherDepartment for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.
Steffi MayerDepartment for Pediatric Surgery, University Hospital of Leipzig, Leipzig, Saxony, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe gastrointestinal tract is particularly vulnerable to strong inflammatory responses during early development as seen in preterm infants with necrotizing enterocolitis (NEC). Intestinal maturation plays a crucial role in the pathogenesis of this condition.

methodsGiven the limited availability of human samples across different stages of gastrointestinal maturation, this study utilised a murine model that closely mirrors the fetal, preterm, term, and adult stages of human development. We investigated baseline and lipopolysaccharide (LPS)-induced inflammatory responses in isolated primary intestinal epithelial cells (IECs) and intraepithelial lymphocytes (IELs).

resultsIECs displayed greater sensitivity to LPS at early developmental stages, with reduced responsiveness as maturation progressed. In contrast, IELs exhibited inflammatory reactivity only at later stages. Regulation of phosphorylated p65 in both cell populations highlighted the role of the TLR-4/NFĸB pathway in these maturation-dependent responses.

conclusionA proinflammatory shift in key epithelial cell populations was observed, reflecting the development of the gastrointestinal system. These findings enhance the understanding of NEC pathogenesis and provide translational insights into intestinal inflammatory responses during maturation. IMPACT: Intestinal epithelial cells (IECs) and intraepithelial lymphocytes (IELs) exhibit contrasting inflammatory responses during gastrointestinal maturation, with IECs being more reactive in early stages and IELs becoming reactive later. This study provides a detailed correlation between human and murine intestinal development, offering insights into maturation-dependent inflammatory mechanisms and the role of the TLR-4/NFĸB pathway. Our findings enhance understanding of gastrointestinal maturation and its role in inflammatory diseases like necrotizing enterocolitis (NEC).

Indexed as

Epithelial CellsGastrointestinal TractInflammationIntestinal MucosaIntestinesIntraepithelial LymphocytesLymphocytesAnimalsEnterocolitis, NecrotizingHumansLipopolysaccharidesMiceMice, Inbred C57BLNF-kappa BSignal TransductionToll-Like Receptor 4LipopolysaccharidesNF-kappa BTlr4 protein, mouseToll-Like Receptor 4Transcription Factor RelA

Identifiers

PMID40691287
PMCPMC13021508

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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.