Evidence map›Paper›PMID 37153622›Full record

ArticleFrontiers in immunology2023

IL-27 induces an IFN-like signature in murine macrophages which in turn modulate colonic epithelium.

Caroline Andrews, Mairi H McLean, Julie A Hixon, Sergio M Pontejo, Tregei Starr, Courtney Malo, Margaret Cam, Lisa Ridnour, Heather Hickman, Olivia Steele-Mortimer and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Modulation of Macrophages TLR4-Mediated Transcriptional Response byInternational journal of molecular sciences · 2025
    Article
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

15 authors at 5 institutions in 2 countries.

Caroline AndrewsLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Mairi H McLeanDivision of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, United Kingdom.
Julie A HixonLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Sergio M PontejoLaboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Tregei StarrRocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.
Courtney MaloViral Immunity and Pathogenesis Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Margaret CamCenter for Cancer Research Collaborative Bioinformatics Resource, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.
Lisa RidnourLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Heather HickmanViral Immunity and Pathogenesis Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
Olivia Steele-MortimerRocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.
David A WinkLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Howard A YoungLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Daniel W McVicarLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Wenqing LiLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Scott K DurumLaboratory of Cancer Innovation, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Center for Cancer Research · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USNational Cancer Institute · USUniversity of Dundee · GB

Funding

The Salmonella-Containing VacuoleZIAAI000909 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI STEELE-MORTIMER, OLIVIA · 2009 to 2025
$12.9M
Chronic Inflammation and CarcinogenesisZIABC011150 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DURUM, SCOTT · 2009 to 2025
$8.5M
6 · The paper itself

Abstract

Mucosal delivery of IL-27 has been shown to have a therapeutic benefit in murine models of inflammatory bowel disease (IBD). The IL-27 effect was associated with phosphorylated STAT1 (pSTAT1), a product of IL27 receptor signaling, in bowel tissue. To determine whether IL-27 acted directly on colonic epithelium, murine colonoids and primary intact colonic crypts were shown to be unresponsive to IL-27

Indexed as

Inflammatory Bowel DiseasesInterleukin-27AnimalsColonEpitheliumMacrophagesMiceInterleukin-27colonoidIBD - inflammatory bowel diseaseIFN signatureIL-27 cytokinemacrophages

Identifiers

PMID37153622
PMCPMC10157156
OpenAlexW4366550653

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.