Evidence map›Paper›PMID 40155377›Full record

ArticleNature communications2025

Type III interferon primes pDCs for TLR7 activation and antagonizes immune suppression mediated by TGF-β and PGE2.

Candice Sakref, Alexis Saby, Céline Rodriguez, Maude Ardin, Lyvia Moudombi, Anne-Claire Doffin, Elisa Gobbini, Aurélien Voissiere, Laurie Besson, Léo Laoubi and 6 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

16 authors.

Candice Sakref *Centre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Alexis Saby *Centre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Céline RodriguezCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Maude ArdinCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Lyvia MoudombiCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Anne-Claire DoffinCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Elisa GobbiniCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Aurélien VoissiereCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.ORCID http://orcid.org/0000-0001-7811-3919
Laurie BessonCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Léo LaoubiCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Jan BöttcherDepartment of Experimental Immunology, Institute of Immunology, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-8163-8107
Stéphane DepilCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Margaux HubertCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.ORCID http://orcid.org/0000-0003-2584-6494
Nathalie Bendriss-VermareCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.ORCID http://orcid.org/0000-0002-8771-3585
Christophe CauxCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France.
Jenny Valladeau-GuilemondCentre de Recherche en Cancérologie de Lyon, Centre Léon Bérard, Université de Lyon, Université Claude Bernard Lyon 1, PLASCAN, INSERM 1052, CNRS, 5286, Lyon, France. jenny.valladeau-guilemond@lyon.unicancer.fr.ORCID http://orcid.org/0000-0003-4160-8867

Funding

Institut National Du Cancer (French National Cancer Institute) PLBIO INCa_4508 and PLBIO INCa_11155
6 · The paper itself

Abstract

Conventional dendritic cell and plasmacytoid dendritic cell (pDC) subsets have specialized functions that can be modulated by the tumor microenvironment, and produce different interferons that are central to antitumor immune responses. While the function of type I interferons in tumor immunity is well characterized, that of type III interferons produced by type 1 conventional dendritic cells in the tumor microenvironment remains unclear. Here we demonstrate in vitro that type III interferons orchestrate pDC survival, activation and TLR7 expression in the blood, thereby enhancing pDC responses to a TLR7 ligand. Moreover, we show that tumor-associated pDCs express the highest level of IFNLR1, and that these immune cell subsets are the most responsive to IFN-III. Importantly, type III interferons prevent the inhibition of pDCs induced by TGF-β or PGE2 in tumor soluble milieu from patients to restores production of IFN-α in pDCs. With TGF-β or PGE2 having pleotropic functions in immune regulation, our results thus implicate IFN-III-mediated immune modulation to have broad impact on various pathological situations.

Indexed as

Dendritic CellsDinoprostoneInterferonsToll-Like Receptor 7Transforming Growth Factor betaFemaleHumansInterferon LambdaTumor MicroenvironmentDinoprostoneInterferon LambdaInterferonsTLR7 protein, humanToll-Like Receptor 7Transforming Growth Factor beta

Identifiers

PMID40155377
PMCPMC11953300

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.