Evidence map›Paper›PMID 34712246›Full record

ReviewFrontiers in immunology2021

Interferon Lambda in the Pathogenesis of Inflammatory Bowel Diseases.

Jonathan W Wallace, David A Constant, Timothy J Nice

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.1field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Interferon Lambda: The Next Frontier in Antiviral Therapy?Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Exposing the Two Contrasting Faces of STAT2 in Inflammation.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2022
    Review
  15. Review
  16. Article
  17. 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

3 authors at 1 institution in 1 country.

Jonathan W WallaceDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, OR, United States.
David A ConstantDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, OR, United States.
Timothy J NiceDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, OR, United States.
Oregon Health & Science University · US

Funding

INTERACTIONS AT THE MICROBE/HOST INTERFACET32AI007472 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LANDFEAR, SCOTT M · 1995 to 2019
$6.7M
Innate immunity to enteric virus infection by IFN?-stimulated-gene expressionR01AI130055 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI Timothy J. Nice · 2017 to 2026
$4.2M
NIAID NIH HHS R01 AI130055NIAID NIH HHS T32 AI007472
6 · The paper itself

Abstract

Interferon λ (IFN-λ) is critical for host viral defense at mucosal surfaces and stimulates immunomodulatory signals, acting on epithelial cells and few other cell types due to restricted IFN-λ receptor expression. Epithelial cells of the intestine play a critical role in the pathogenesis of Inflammatory Bowel Disease (IBD), and the related type II interferons (IFN-γ) have been extensively studied in the context of IBD. However, a role for IFN-λ in IBD onset and progression remains unclear. Recent investigations of IFN-λ in IBD are beginning to uncover complex and sometimes opposing actions, including pro-healing roles in colonic epithelial tissues and potentiation of epithelial cell death in the small intestine. Additionally, IFN-λ has been shown to act through non-epithelial cell types, such as neutrophils, to protect against excessive inflammation. In most cases IFN-λ demonstrates an ability to coordinate the host antiviral response without inducing collateral hyperinflammation, suggesting that IFN-λ signaling pathways could be a therapeutic target in IBD. This mini review discusses existing data on the role of IFN-λ in the pathogenesis of inflammatory bowel disease, current gaps in the research, and therapeutic potential of modulating the IFN-λ-stimulated response.

Indexed as

AnimalsApoptosisCytokinesEpithelial CellsHumansImmunity, InnateInflammatory Bowel DiseasesInterferon LambdaInterferonsIntestinal MucosaModels, ImmunologicalProtein IsoformsSignal TransductionSTAT Transcription FactorsTight JunctionsCytokinesInterferon LambdaInterferonsProtein IsoformsSTAT Transcription FactorsCrohn’s disease (CD)inflammatory bowel disease (IBD)interferon lambda (IFN-λ)intestinal epithelial cell (IEC)ulcerative colitis (UC)

Identifiers

PMID34712246
PMCPMC8547615
OpenAlexW3207141888

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.