Evidence map›Paper›PMID 38563819›Full record

ArticleThe Journal of experimental medicine2024

NF-κB subunits RelA and c-Rel selectively control CD4+ T cell function in multiple sclerosis and cancer.

Guilhem Lalle, Raphaëlle Lautraite, Khaled Bouherrou, Maud Plaschka, Aurora Pignata, Allison Voisin, Julie Twardowski, Marlène Perrin-Niquet, Pierre Stéphan, Sarah Durget and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  4. NF-κB in inflammation and cancer.Cellular & molecular immunology · 2025
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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

27 authors at 6 institutions in 4 countries.

Guilhem Lalle *Cancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-8861-9523
Raphaëlle Lautraite *Cancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-3437-5666
Khaled BouherrouCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0005-4116-5180
Maud PlaschkaCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0003-1137-7623
Aurora PignataToulouse Institute for Infectious and Inflammatory Diseases (Infinity), UMR INSERM 1291, CNRS 5051, Université Toulouse III , Toulouse, France.ORCID 0000-0002-9806-1498
Allison VoisinCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0003-0715-9391
Julie TwardowskiCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0006-4788-1193
Marlène Perrin-NiquetCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0006-1496-4590
Pierre StéphanCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0001-5999-284X
Sarah DurgetCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0002-6484-4037
Laurie TononCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, Gilles Thomas Bioinformatics Platform, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0005-8794-7276
Maude ArdinCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, Gilles Thomas Bioinformatics Platform, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0009-0005-4798-9009
Cyril DegletagneCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-5363-2381
Alain ViariCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, Gilles Thomas Bioinformatics Platform, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-1329-7777
Laurence Belgarbi DutronBiology Department, Ecole Normale Supérieure of Lyon, Lyon, France.ORCID 0009-0006-4848-5731
Nathalie DavoustLaboratory of Biology and Modelling of the Cell, Ecole Normale Supérieure of Lyon, CNRS UMR 5239, INSERM U1293 , Lyon, France.ORCID 0009-0006-0737-2941
Thomas S PostlerDepartment of Microbiology and Immunology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.ORCID 0000-0002-3558-9084
Jingyao ZhaoDepartment of Microbiology and Immunology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.ORCID 0009-0008-8437-9842
Christophe CauxCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0003-2438-833X
Julie CaramelCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-8883-918X
Stéphane DalleCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-3423-4548
Philippe A CassierCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0003-3857-1688
Ulf KleinDivision of Haematology and Immunology, Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, UK.ORCID 0000-0002-4789-967X
Marc Schmidt-SupprianInstitute of Experimental Hematology, School of Medicine, Technical University of Munich , Munich, Germany.ORCID 0000-0002-8543-6166
Roland LiblauToulouse Institute for Infectious and Inflammatory Diseases (Infinity), UMR INSERM 1291, CNRS 5051, Université Toulouse III , Toulouse, France.ORCID 0000-0001-5477-5475
Sankar GhoshDepartment of Microbiology and Immunology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.ORCID 0000-0002-3227-0588
Yenkel Grinberg-BleyerCancer Research Center of Lyon, Labex DEV2CAN, Institut Convergence Plascan, Centre Léon Bérard, UMR INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1 , Lyon, France.ORCID 0000-0002-3515-8305
Université Claude Bernard Lyon 1 · FRColumbia University · USCentre National de la Recherche Scientifique · FRÉcole Normale Supérieure de Lyon · FRGerman Cancer Research Center · DEUniversity of Leeds · GB

Funding

ARC FoundationARSEP FoundationCentre National de la Recherche ScientifiqueFondation pour la Recherche MédicaleInstitut National de la Santé et de la Recherche MédicaleLabex DEVweCAN ANR-10-LABX-0061
6 · The paper itself

Abstract

The outcome of cancer and autoimmunity is often dictated by the effector functions of CD4+ conventional T cells (Tconv). Although activation of the NF-κB signaling pathway has long been implicated in Tconv biology, the cell-autonomous roles of the separate NF-κB transcription-factor subunits are unknown. Here, we dissected the contributions of the canonical NF-κB subunits RelA and c-Rel to Tconv function. RelA, rather than c-Rel, regulated Tconv activation and cytokine production at steady-state and was required for polarization toward the TH17 lineage in vitro. Accordingly, RelA-deficient mice were fully protected against neuroinflammation in a model of multiple sclerosis due to defective transition to a pathogenic TH17 gene-expression program. Conversely, Tconv-restricted ablation of c-Rel impaired their function in the microenvironment of transplanted tumors, resulting in enhanced cancer burden. Moreover, Tconv required c-Rel for the response to PD-1-blockade therapy. Our data reveal distinct roles for canonical NF-κB subunits in different disease contexts, paving the way for subunit-targeted immunotherapies.

Indexed as

Multiple SclerosisNeoplasmsAnimalsCD4-Positive T-LymphocytesMiceNF-kappa BProto-Oncogene Proteins c-relSignal TransductionTranscription Factor RelATumor MicroenvironmentNF-kappa BProto-Oncogene Proteins c-relRela protein, mouseTranscription Factor RelA

Identifiers

PMID38563819
PMCPMC10986815
OpenAlexW4393419944

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

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.