Evidence map›Paper›PMID 39500322›Full record

ArticleCell2024

Type III interferons induce pyroptosis in gut epithelial cells and impair mucosal repair.

Kautilya K Jena, Julien Mambu, Daniel Boehmer, Benedetta Sposito, Virginie Millet, Joshua de Sousa Casal, Hayley I Muendlein, Roberto Spreafico, Romain Fenouil, Lionel Spinelli and 21 more

Abstract read
In one paragraph

Article in Cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–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

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. The gasdermin family: from pyroptosis mechanisms to therapeutic targets.Signal transduction and targeted therapy · 2026
    Review
  5. Article
  6. Article
  7. Structural and molecular principles of DAMP biology.Nature structural & molecular biology · 2026
    Review
  8. Berberine AlleviatesInternational journal of molecular sciences · 2026
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

31 authors.

Kautilya K JenaDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Julien MambuAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Daniel BoehmerDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Department of Medicine II, University Hospital, LMU Munich, 81377 Munich, Germany.
Benedetta SpositoDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Virginie MilletAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Joshua de Sousa CasalDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Program in Immunology, Harvard Medical School, Boston, MA 02115, USA.
Hayley I MuendleinDepartment of Immunology, Tufts University School of Medicine, Boston, MA 02111, USA.
Roberto SpreaficoInstitute for Quantitative and Computational Biosciences, University of California, Los Angeles, CA, USA.
Romain FenouilAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Lionel SpinelliAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Sarah WurbelAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Chloé RiquierAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Franck GallandAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Philippe NaquetAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Lionel ChassonAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France.
Megan ElkinsDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Vanessa MitsialisDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Natália Ketelut-CarneiroProgram in Innate Immunity, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA 01655, USA.
Katlynn Bugda GwiltDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Jay R ThiagarajahDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Hai-Bin RuanDepartment of Integrative Biology and Physiology, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Zhaoyu LinState Key Laboratory of Pharmaceutical Biotechnology, Ministry of Education Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, National Resource Center for Mutant Mice of China, Nanjing Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing 210061, China.
Egil LienProgram in Innate Immunity, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA 01655, USA; Center for Molecular inflammation Research, Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway.
Feng ShaoNational Institute of Biological Sciences, Beijing 102206, China.
Janet ChouDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Alexander PoltorakDepartment of Immunology, Tufts University School of Medicine, Boston, MA 02111, USA.
Jose Ordovas-MontanesDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Program in Immunology, Harvard Medical School, Boston, MA 02115, USA.
Katherine A FitzgeraldProgram in Innate Immunity, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA 01655, USA.
Scott B SnapperDivision of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA.
Achille BroggiAix Marseille Université, CNRS, INSERM, Centre d'Immunologie de Marseille-Luminy (CIML), 13288 Marseille Cedex, France. Electronic address: broggi@ciml.univ-mrs.fr.
Ivan ZanoniDivision of Immunology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Division of Gastroenterology, Harvard Medical School and Boston Children's Hospital, Boston, MA 02115, USA; Program in Immunology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: ivan.zanoni@childrens.harvard.edu.

Funding

Type III interferon Control of Mucosal ImmunityR01DK115217 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Scott B Snapper, Ivan Zanoni · 2017 to 2026
$5.6M
Caspase-8 as a focal hub in effector-triggered immunityR01AI146855 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIEN, EGIL · 2019 to 2023
$2.9M
RNA splicing factor Raver1 controls cell death, inflammation, and innateimmunityR01AI181309 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Egil Lien · 2024 to 2026
$2.5M
NIAID NIH HHS R01 AI146855NIAID NIH HHS R01 AI181309NIDDK NIH HHS R01 DK115217
6 · The paper itself

Abstract

Tissue damage and repair are hallmarks of inflammation. Despite a wealth of information on the mechanisms that govern tissue damage, mechanistic insight into how inflammation affects repair is lacking. Here, we investigated how interferons influence tissue repair after damage to the intestinal mucosa. We found that type III, not type I or type II, interferons delay epithelial cell regeneration by inducing the upregulation of Z-DNA-binding protein 1 (ZBP1). Z-nucleic acids formed following intestinal damage are sensed by ZBP1, leading to caspase-8 activation and the cleavage of gasdermin C (GSDMC). Cleaved GSDMC drives epithelial cell death by pyroptosis and delays repair of the large or small intestine after colitis or irradiation, respectively. The type III interferon/ZBP1/caspase-8/GSDMC axis is also active in patients with inflammatory bowel disease (IBD). Our findings highlight the capacity of type III interferons to delay gut repair, which has implications for IBD patients or individuals exposed to radiation therapies.

Indexed as

Epithelial CellsInterferon LambdaInterferonsIntestinal MucosaPyroptosisAnimalsCaspase 8ColitisFemaleHumansInflammatory Bowel DiseasesMaleMiceMice, Inbred C57BLRegenerationRNA-Binding ProteinsCaspase 8Interferon LambdaInterferonsRNA-Binding Proteinscolitisdamagegasdermininflammationinflammatory bowel diseaseinterferonsintestinal epithelial cellintestinal stem cellirradiationpattern recognition receptorspyroptosisrepairZ-nucleic acid

Identifiers

PMID39500322
PMCPMC11682936

What OpenQuestion holds

Textmetadata
LicenceTDM
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.