Evidence map›Paper›PMID 30939120›Full record

ArticleThe Journal of clinical investigation2019

IL-7 receptor influences anti-TNF responsiveness and T cell gut homing in inflammatory bowel disease.

Lyssia Belarif, Richard Danger, Laetitia Kermarrec, Véronique Nerrière-Daguin, Sabrina Pengam, Tony Durand, Caroline Mary, Elise Kerdreux, Vanessa Gauttier, Aneta Kucik and 29 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 2 pooled it
10.6field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 2 syntheses or guidelines pooled it, 127 citations in OpenAlex.

  1. Identification ofFrontiers in immunology · 2026
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  11. Enteric nervous system as a therapeutic target in gastrointestinal disorders.World journal of gastrointestinal pharmacology and therapeutics · 2025
    Article
  12. WTAP-mediated mHuman cell · 2025
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15 more citing papers are in PubMed but not listed here.

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

39 authors at 8 institutions in 5 countries.

Lyssia BelarifOSE Immunotherapeutics, Nantes, France.
Richard DangerCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Laetitia KermarrecInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Véronique Nerrière-DaguinCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Sabrina PengamOSE Immunotherapeutics, Nantes, France.
Tony DurandInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Caroline MaryOSE Immunotherapeutics, Nantes, France.
Elise KerdreuxCHU Nantes, IMAD, Nantes, France.
Vanessa GauttierOSE Immunotherapeutics, Nantes, France.
Aneta KucikBlizard Institute, Barts and The London School of Medicine and Dentistry, London, United Kingdom.
Virginie ThepenierOSE Immunotherapeutics, Nantes, France.
Jerome C MartinPrecision Immunology Institute.
Christie ChangPrecision Immunology Institute.
Adeeb RahmanPrecision Immunology Institute.
Nina Salabert-Le GuenCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Cécile BraudeauCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Ahmed AbidiCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Grégoire DavidInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Florent MalardCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Celine TakoudjuInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Bernard MartinetCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Nathalie GérardCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Isabelle NeveuInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Michel NeunlistInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Emmanuel CoronInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Thomas T MacDonaldBlizard Institute, Barts and The London School of Medicine and Dentistry, London, United Kingdom.
Pierre DesreumauxHepato-Gastroenterology Department, Claude Huriez Hospital, University of Lille 2, Lille, France.
Hoa-Le MaiCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Stephanie Le Bas-BernardetCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Jean-François MosnierCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Miriam MeradPrecision Immunology Institute.
Régis JosienCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Sophie BrouardCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Jean-Paul SoulillouCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Gilles BlanchoCentre de Recherche en Transplantation et Immunologie (CRTI), UMR 1064, Inserm, Université de Nantes, Nantes, France.
Arnaud BourreilleInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Philippe NaveilhanInstitut des Maladies de l'Appareil Digestif (IMAD), The Enteric Nervous System in Gut and Brain Disorders, Université de Nantes, INSERM, Nantes, France.
Bernard VanhoveOSE Immunotherapeutics, Nantes, France.
Nicolas PoirierOSE Immunotherapeutics, Nantes, France.
Inserm · FROSE Immunotherapeutics (France) · FRCancer Institute (WIA) · INQueen Mary University of London · GBCentre Hospitalier Universitaire de Nantes · FRIcahn School of Medicine at Mount Sinai · USTunis University · TNUniversité de Lille · FR

Funding

Harnessing Csf-2 compartmentalized role on tissue resident phagocytes to uncouple anti-tumoral from pathological immunity induced by checkpoint inhibitorsR01CA190400 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MERAD, MIRIAM · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA190400
6 · The paper itself

Abstract

It remains unknown what causes inflammatory bowel disease (IBD), including signaling networks perpetuating chronic gastrointestinal inflammation in Crohn's disease (CD) and ulcerative colitis (UC), in humans. According to an analysis of up to 500 patients with IBD and 100 controls, we report that key transcripts of the IL-7 receptor (IL-7R) pathway are accumulated in inflamed colon tissues of severe CD and UC patients not responding to either immunosuppressive/corticosteroid, anti-TNF, or anti-α4β7 therapies. High expression of both IL7R and IL-7R signaling signature in the colon before treatment is strongly associated with nonresponsiveness to anti-TNF therapy. While in mice IL-7 is known to play a role in systemic inflammation, we found that in humans IL-7 also controlled α4β7 integrin expression and imprinted gut-homing specificity on T cells. IL-7R blockade reduced human T cell homing to the gut and colonic inflammation in vivo in humanized mouse models, and altered effector T cells in colon explants from UC patients grown ex vivo. Our findings show that failure of current treatments for CD and UC is strongly associated with an overexpressed IL-7R signaling pathway and point to IL-7R as a relevant therapeutic target and potential biomarker to fill an unmet need in clinical IBD detection and treatment.

Indexed as

AdolescentAdultAgedAnimalsColitis, UlcerativeColonCrohn DiseaseCytokinesEndoscopyFemaleGene Expression ProfilingGene Expression RegulationGraft vs Host DiseaseHumansInflammationIntegrinsCytokinesintegrin alpha4beta7IntegrinsReceptors, Interleukin-7Tumor Necrosis Factor-alphaCytokinesGastroenterologyImmunologyInflammatory bowel diseaseT cells

Identifiers

PMID30939120
PMCPMC6486337
OpenAlexW2931571227

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.