Evidence map›Paper›PMID 41331250›Full record

ArticleNature communications2025

Physiological activation of Aryl hydrocarbon receptor by food-derived ligands is essential for the efficacy of anti-PD1 therapy.

Alba De Juan, Alice Coillard, Adeline Cros, Alessandra Rigamonti, Lamine Alaoui, Julio L Sampaio, Natacha Monot, Aurélie Balvay, Anne Foussier, Mathilde Rieux-Laucat 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. 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.

Alba De Juan *Institut Curie, PSL University, INSERM, U932, Paris, France.ORCID http://orcid.org/0000-0003-0174-4389
Alice Coillard *Institut Curie, PSL University, INSERM, U932, Paris, France.
Adeline CrosInstitut Curie, PSL University, INSERM, U932, Paris, France.
Alessandra RigamontiInstitut Curie, PSL University, INSERM, U932, Paris, France.
Lamine AlaouiInstitut Curie, PSL University, INSERM, U932, Paris, France.
Julio L SampaioInstitut Curie, PSL University, Plateforme de Métabolomique et Lipidomique, Paris, France.
Natacha MonotInstitut Curie, PSL University, INSERM, U932, Paris, France.
Aurélie BalvayUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Anne FoussierUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Mathilde Rieux-LaucatInstitut Curie, PSL University, INSERM, U932, Paris, France.
Léa GuyonnetInstitut Curie, PSL University, Plateforme de Cytométrie de Flux, Paris, France.
Sylvie RabotUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID http://orcid.org/0000-0002-4603-2038
Christian VosshenrichImmunology Department, Institut Pasteur, INSERM, U1223, Innate Immunity Unit, Paris, France.ORCID http://orcid.org/0000-0002-4407-8649
Elodie SeguraInstitut Curie, PSL University, INSERM, U932, Paris, France. elodie.segura@inserm.fr.ORCID http://orcid.org/0000-0003-1795-1921

Funding

Cancer Research Institute (CRI) CLIP grant CRI4215EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) Marie Curie Actions No 842535Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) PJA20171206249Fondation pour la Recherche Médicale (Foundation for Medical Research in France) FDT202001010805Institut National Du Cancer (French National Cancer Institute) 2018-1-PLBIO-01-ICR1Ligue Contre le Cancer RS18/75-23
6 · The paper itself

Abstract

Cancer immuno-surveillance and response to therapy are affected by environmental factors, including nutrition. However, the direct effects of individual nutrients remain poorly understood. Here we investigate the impact of dietary ligands of Aryl hydrocarbon receptor (AhR), a transcription factor activated by tryptophan catabolites generated through food digestion and microbiota metabolism. By analyzing pre-clinical tumor models in mice fed on a diet naturally poor in AhR ligands or the same diet supplemented with Indole-3-carbinol, we show that diet-derived AhR ligands are required for the optimal efficacy of anti-PD1 therapy. Using conditional knockout mice, we evidence an essential role for AhR in CD8 T cells, but not NK cells or myeloid cells. Mechanistically, AhR promotes anti-PD1-mediated reinvigoration of progenitor exhausted CD8 T cells and licences the functional response of effector CD8 T cells. Our work allows a better understanding of the role of nutrients in anti-tumor immune responses and has implications for the rational design of dietary interventions for improving the efficacy of checkpoint blockade therapy.

Indexed as

Basic Helix-Loop-Helix ProteinsImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorReceptors, Aryl HydrocarbonAnimalsCD8-Positive T-LymphocytesCell Line, TumorDietFemaleHumansIndolesKiller Cells, NaturalLigandsMiceMice, Inbred C57BLMice, KnockoutAhr protein, mouseBasic Helix-Loop-Helix ProteinsImmune Checkpoint Inhibitorsindole-3-carbinolIndolesLigandsPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorReceptors, Aryl HydrocarbonTryptophan

Identifiers

PMID41331250
PMCPMC12672584

What Socratic holds

Textmetadata
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 Socratic graph.