Evidence map›Paper›PMID 33408718›Full record

ReviewFrontiers in immunology2020

Context Is Key: Delineating the Unique Functions of IFNα and IFNβ in Disease.

Lindsey E Fox, Marissa C Locke, Deborah J Lenschow

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. IFNIKB: a type I interferon database for antitumuor immunity studies.Database : the journal of biological databases and curation · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Immunomodulatory Role of Interferons in Viral and Bacterial Infections.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Alum-anchored intratumoral retention improves the tolerability and antitumor efficacy of type I interferon therapies.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. 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

3 authors at 1 institution in 1 country.

Lindsey E FoxDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, United States.
Marissa C LockeDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, United States.
Deborah J LenschowDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, United States.
Washington University in St. Louis · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
IFN Dependent Control of Acute and Chronic Chikungunya Virus Induced DiseaseR01AI127513 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, LENSCHOW, DEBORAH J · 2017 to 2020
$2.1M
IDENTIFICATION OF MECHANISMS CONTRIBUTING TO CHIKUNGUNYA VIRUS INDUCED CHRONIC ARTHRITISR21AI135490 · NIAID · WASHINGTON UNIVERSITY · PI LENSCHOW, DEBORAH J · 2018 to 2019
$419k
The role of type I interferons during chikungunya virus infectionF31AI149999 · NIAID · WASHINGTON UNIVERSITY · PI LOCKE, MARISSA CHRISTINE · 2020 to 2021
$36k
NCI NIH HHS T32 CA009547NIAID NIH HHS F31 AI149999NIAID NIH HHS R01 AI127513NIAID NIH HHS R21 AI135490NIAID NIH HHS T32 AI007163
6 · The paper itself

Abstract

Type I interferons (IFNs) are critical effector cytokines of the immune system and were originally known for their important role in protecting against viral infections; however, they have more recently been shown to play protective or detrimental roles in many disease states. Type I IFNs consist of IFNα, IFNβ, IFNϵ, IFNκ, IFNω, and a few others, and they all signal through a shared receptor to exert a wide range of biological activities, including antiviral, antiproliferative, proapoptotic, and immunomodulatory effects. Though the individual type I IFN subtypes possess overlapping functions, there is growing appreciation that they also have unique properties. In this review, we summarize some of the mechanisms underlying differential expression of and signaling by type I IFNs, and we discuss examples of differential functions of IFNα and IFNβ in models of infectious disease, cancer, and autoimmunity.

Indexed as

AnimalsAutoimmune DiseasesAutoimmunityCommunicable DiseasesHost-Pathogen InteractionsHumansInterferon-alphaInterferon-betaLigandsNeoplasmsReceptors, InterferonSignal TransductionTumor MicroenvironmentInterferon-alphaInterferon-betaLigandsReceptors, InterferonautoimmunitycancerIFNα subtypesIFNβinfectiontype I interferons

Identifiers

PMID33408718
PMCPMC7779635
OpenAlexW3116115234

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.