Evidence map›Paper›PMID 31819956›Full record

ArticleThe Journal of experimental medicine2020

Loss of IL-10 signaling in macrophages limits bacterial killing driven by prostaglandin E2.

Subhankar Mukhopadhyay, Eva Heinz, Immacolata Porreca, Kaur Alasoo, Amy Yeung, Huei-Ting Yang, Tobias Schwerd, Jessica L Forbester, Christine Hale, Chukwuma A Agu and 12 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Prostaglandin ENature communications · 2024
    Article
  13. Review
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  15. Review
  16. Article
  17. Article
  18. Single-cell profiling identifies ACEScience advances · 2023
    Article
  19. Review
  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

22 authors at 6 institutions in 3 countries.

Subhankar MukhopadhyayWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Eva HeinzWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Immacolata PorrecaWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Kaur AlasooWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Amy YeungWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Huei-Ting YangTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Tobias SchwerdTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Jessica L ForbesterWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Christine HaleWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Chukwuma A AguWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Yoon Ha ChoiWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Julia RodriguesWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Melania CapitaniTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Luke Jostins-DeanThe Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
David C ThomasDepartment of Medicine, University of Cambridge, University of Cambridge School of Clinical Medicine, Cambridge, UK.
Simon TravisTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Daniel GaffneyWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
William C SkarnesWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Nicholas ThomsonWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Holm H UhligTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Gordon DouganWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Fiona PowrieTranslational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Wellcome Sanger Institute · GBJohn Radcliffe Hospital · GBUniversity of Cambridge · GBKing's College London · GBUniversity of London · GBUniversity of Oxford · GB

Funding

Department of HealthWellcome Trust
6 · The paper itself

Abstract

Loss of IL-10 signaling in macrophages (Mφs) leads to inflammatory bowel disease (IBD). Induced pluripotent stem cells (iPSCs) were generated from an infantile-onset IBD patient lacking a functional IL10RB gene. Mφs differentiated from IL-10RB-/- iPSCs lacked IL-10RB mRNA expression, were unable to phosphorylate STAT3, and failed to reduce LPS induced inflammatory cytokines in the presence of exogenous IL-10. IL-10RB-/- Mφs exhibited a striking defect in their ability to kill Salmonella enterica serovar Typhimurium, which was rescuable after experimentally introducing functional copies of the IL10RB gene. Genes involved in synthesis and receptor pathways for eicosanoid prostaglandin E2 (PGE2) were more highly induced in IL-10RB-/- Mφs, and these Mφs produced higher amounts of PGE2 after LPS stimulation compared with controls. Furthermore, pharmacological inhibition of PGE2 synthesis and PGE2 receptor blockade enhanced bacterial killing in Mφs. These results identify a regulatory interaction between IL-10 and PGE2, dysregulation of which may drive aberrant Mφ activation and impaired host defense contributing to IBD pathogenesis.

Indexed as

Cell DifferentiationCells, CulturedDinoprostoneFemaleGene Knockout TechniquesHumansInduced Pluripotent Stem CellsInflammationInflammatory Bowel DiseasesInterleukin-10Interleukin-10 Receptor alpha SubunitInterleukin-10 Receptor beta SubunitLipopolysaccharidesMacrophage ActivationMacrophagesMutationDinoprostoneIL10 protein, humanIL10RB protein, humanInterleukin-10Interleukin-10 Receptor alpha SubunitInterleukin-10 Receptor beta SubunitLipopolysaccharidesSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID31819956
PMCPMC7041704
OpenAlexW2991882421

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.