Evidence map›Paper›PMID 40303843›Full record

ArticleDiscovery immunology2025

Dynamic roles of ILC3 in endometrial repair and regeneration.

Antonia O Cuff, Ee Von Woon, Thomas Bainton, Brendan Browne, Phoebe M Kirkwood, Frances Collins, Douglas A Gibson, Philippa T K Saunders, Andrew W Horne, Mark R Johnson and 2 more

Abstract read
In one paragraph

Article in Discovery immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Mesenchymal stem cells for recurrent miscarriage.Journal of translational medicine · 2026
    Review
  3. Innate Lymphoid Cells in Reproductive Health and Disease.European journal of immunology · 2025
    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

12 authors.

Antonia O CuffDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Ee Von WoonDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID https://orcid.org/0000-0002-4787-1546
Thomas BaintonDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Brendan BrowneDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Phoebe M KirkwoodCentre for Reproductive Health, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Frances CollinsCentre for Reproductive Health, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Douglas A GibsonCentre for Reproductive Health, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0002-9949-1983
Philippa T K SaundersCentre for Reproductive Health, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0001-9051-9380
Andrew W HorneCentre for Reproductive Health, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0002-9656-493X
Mark R JohnsonDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID https://orcid.org/0000-0003-1096-9918
David A MacIntyreDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID https://orcid.org/0000-0002-4186-5567
Victoria MaleDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID https://orcid.org/0000-0001-5654-5083

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Innate lymphoid cells (ILCs) are prominent in the human uterine mucosa and play physiological roles in pregnancy. ILC3 are the second-most common ILC subset in the uterine mucosa, but their role remains unclear. Methods: Here we define two subsets of lineage-negative CD56+ CD117+ CRTH2-uterine ILC3, distinguished by their expression of CD127. Results: The CD127- subset is most numerous and active during menstruation and immediately after parturition, suggesting a role in the repair of the uterine mucosa (called endometrium outside of pregnancy); the CD127+ subset is most numerous and active immediately after menstruation, as the endometrium regenerates. In healthy endometrium, ILC3 are spatially associated with glandular epithelial and endothelial cells, which both express receptors for the ILC3-derived cytokines, IL-22 and IL-8. In the eutopic endometrium of people with endometriosis, ILC3 are located further from glandular epithelial and endothelial cells suggesting that these cells may be less exposed to ILC3 products, potentially with negative consequences for endometrial regeneration. Conclusion: Our findings highlight the dynamic nature of ILC3 in the uterine mucosa and suggest their primary role is in repair and regeneration. An improved understanding of uterine ILC3 will inform future research on endometrial health and disease.

Indexed as

endometriosisendometriuminnate lymphoid cellmucosal immunologyreproductive immunology

Identifiers

PMID40303843
PMCPMC12038238

What OpenQuestion holds

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Registered trials

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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.