Evidence map›Paper›PMID 40213548›Full record

ArticleFrontiers in immunology2025

A secreted helminth microRNA suppresses gastrointestinal cell differentiation required for innate immunity.

Matias G Perez, Victoria Gillan, William M Anderson, François Gerbe, Fabien Herbert, Tom N McNeilly, Rick M Maizels, Philippe Jay, Eileen Devaney, Collette Britton

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Current research in parasitology & vector-borne diseases · 2025
    Article
  7. Review
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

10 authors.

Matias G PerezSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.
Victoria GillanSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.
William M AndersonSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.
François GerbeInstitute of Functional Genomics (IGF), University of Montpellier, CNRS, Inserm, Montpellier, France.
Fabien HerbertInstitute of Functional Genomics (IGF), University of Montpellier, CNRS, Inserm, Montpellier, France.
Tom N McNeillyDisease Control Department, Moredun Research Institute, Penicuik, United Kingdom.
Rick M MaizelsCentre for Parasitology, School of Infection and Immunity, University of Glasgow, Glasgow, United Kingdom.
Philippe JayInstitute of Functional Genomics (IGF), University of Montpellier, CNRS, Inserm, Montpellier, France.
Eileen DevaneySchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.
Collette BrittonSchool of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogens have developed multiple strategies to modulate host immune defense mechanisms. Understanding how this is achieved has potential to inform novel therapeutics for diseases caused by immune dysfunction. Parasitic helminths are masters of immune evasion, via release of secreted products, resulting in chronic infection. Helminths secrete small regulatory microRNA (miRNAs), which can interact with host cells. Here we show that a single parasite miRNA (miR-5352), conserved across gastrointestinal (GI) nematodes, suppresses IL-13-induced GI epithelial cell differentiation and cytokine responses, and promotes stem cell maintenance. Mechanistically, this is achieved through targeted repression of critical host factors, including Klf-4 and the IL-22 receptor, together with modulation of Wnt and Notch signalling pathways. Nematode miR-5352 shows seed sequence conservation with mammalian miR-92a family members, indicating that through convergent evolution, GI nematodes exploit a host miRNA regulatory network to suppress host innate responses, promote tissue regeneration and establish a favourable environment for chronic infection.

Indexed as

Cell DifferentiationImmunity, InnateMicroRNAsRNA, HelminthAnimalsEpithelial CellsHost-Parasite InteractionsHumansInterleukin-13Kruppel-Like Factor 4MiceInterleukin-13Klf4 protein, mouseKruppel-Like Factor 4MicroRNAsRNA, HelminthIL-13innate immunitymicroRNAsnematode parasitesorganoidsstem cellstuft cells

Identifiers

PMID40213548
PMCPMC11983496

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.