Evidence map›Paper›PMID 40610398›Full record

ArticleNature communications2025

Interleukin-35 impairs human NK cell effector functions and induces their ILC1-like conversion with tissue residency features.

Valentin Picant, Lara Revol-Bauz, Laurie Tonon, Timothée Casini, Aurélien Voissière, Dominique Poujol, Emilie Picard, Céline Rodriguez, Cyril Degletagne, Emily Sible and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Interleukin-18 armours antitumour immune effectors.Nature reviews. Immunology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. 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

14 authors.

Valentin Picant *CISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.ORCID http://orcid.org/0000-0001-9514-0492
Lara Revol-Bauz *CISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Laurie TononSynergie-Lyon-Cancer Fundation, Centre Léon Bérard, Lyon, France.ORCID http://orcid.org/0009-0005-8794-7276
Timothée CasiniCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Aurélien VoissièreCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.ORCID http://orcid.org/0000-0001-7811-3919
Dominique PoujolCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Emilie PicardCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Céline RodriguezCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Cyril DegletagneGenomic platform, Centre de Recherche en Cancérologie de Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Emily SibleCentre International de Recherche en Infectiologie, CIRI, INSERM U1111, Lyon, France.
Uzma HasanLyon Immunotherapy for Cancer Laboratory (LICL), Centre Léon Bérard, Lyon, France.ORCID http://orcid.org/0000-0002-1770-5539
Anthony FerrariSynergie-Lyon-Cancer Fundation, Centre Léon Bérard, Lyon, France.
Christophe CauxCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France.
Nathalie Bendriss-VermareCISTAR team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, Université de Lyon, Université Lyon 1, Centre Léon Bérard, Lyon, France. nathalie.bendriss-vermare@lyon.unicancer.fr.ORCID http://orcid.org/0000-0002-8771-3585

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-11-IDEX-0007Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) PJA20181208305Institut National Du Cancer (French National Cancer Institute) INCa-DGOS-INSERM-ITMO cancerInstitut National Du Cancer (French National Cancer Institute) PLBIO-16-116Ligue Contre le Cancer EL2020.LNCC-CHC
6 · The paper itself

Abstract

Natural Killer (NK) cells play pivotal immunological roles including direct cytotoxic effector function and secretion of inflammatory and immunomodulating cytokines. In the context of chronic inflammation, NK cell fitness decreases during disease progression through currently unknown mechanisms. Here, we demonstrate that Interleukin-35 (IL-35) inhibits human NK cell proliferation, pro-inflammatory, and cytotoxic functions, while promoting secretion of TGF-β and proangiogenic factors in vitro. We show prolonged exposure to IL-35 converts both conventional and adaptive NK cells into CD9

Indexed as

InterleukinsKiller Cells, NaturalCell PlasticityCell ProliferationHumansNeoplasmsTransforming Growth Factor betaTumor Microenvironmentinterleukin-35, humanInterleukinsTransforming Growth Factor beta

Identifiers

PMID40610398
PMCPMC12229632

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.