Evidence map›Paper›PMID 31771761›Full record

ReviewSeminars in immunology2019

Type III IFNs: Beyond antiviral protection.

Sergei V Kotenko, Amariliz Rivera, Dane Parker, Joan E Durbin

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

5 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 1 country.

Sergei V KotenkoDepartment of Microbiology, Biochemistry and Molecular Genetics, Newark, NJ, 07103, USA; Center for Cell Signaling, Newark, NJ, 07103, USA; Center for Immunity and Inflammation, Rutgers New Jersey Medical School, RBHS, Newark, NJ, 07103, USA. Electronic address: kotenkse@njms.rutgers.edu.
Amariliz RiveraDepartment of Pediatrics, Newark, NJ, 07103, USA; Center for Immunity and Inflammation, Rutgers New Jersey Medical School, RBHS, Newark, NJ, 07103, USA.
Dane ParkerDepartment of Pathology, Immunology and Laboratory Medicine, Newark, NJ, 07103, USA; Center for Immunity and Inflammation, Rutgers New Jersey Medical School, RBHS, Newark, NJ, 07103, USA.
Joan E DurbinDepartment of Pathology, Immunology and Laboratory Medicine, Newark, NJ, 07103, USA; Center for Immunity and Inflammation, Rutgers New Jersey Medical School, RBHS, Newark, NJ, 07103, USA. Electronic address: durbinje@njms.rutgers.edu.
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · USUniversity Hospital, Newark · US

Funding

Development of IFN-lambda3 for the Prevention and Treatment of Virus InfectionR01AI104669 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI DURBIN, JOAN E., KOTENKO, SERGEI V · 2013 to 2017
$5.9M
Role of Interferon-lambda in Antiviral ResponseR01AI057468 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KOTENKO, SERGEI V · 2005 to 2009
$1.9M
ROLE OF TYPE III INTERFERONS IN STAPHYLOCOCCUS AUREUS RESPIRATORY TRACT INFECTIONR01HL134870 · NHLBI · RBHS-NEW JERSEY MEDICAL SCHOOL · PI PARKER, DANE · 2017 to 2020
$1.8M
Regulation of antifungal immunity by monocyte-derived dendritic cellsR01AI114647 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI RIVERA, AMARILIZ · 2015 to 2019
$1.8M
NHLBI NIH HHS R01 HL134870NIAID NIH HHS R01 AI057468NIAID NIH HHS R01 AI104669NIAID NIH HHS R01 AI114647
6 · The paper itself

Abstract

The unexpected discovery of a novel family of antiviral mediators, type III IFNs or IFN-λs, challenged the widely accepted primacy of type I IFNs in antiviral immunity, and it is now well recognized that the IFN-λ-based antiviral system plays a major role in antiviral protection of epithelial barriers. The recent characterization of previously unknown IFN-λ-mediated activities has prompted further reassessment of the role of type I IFNs in innate and adaptive immune and inflammatory responses. Since type I and type III IFNs are co-produced in response to a variety of stimuli, it is likely that many physiological processes are simultaneously and coordinately regulated by these cytokines in pathological conditions, and likely at steady state, as baseline expression of both IFN types is maintained by microbiota. In this review, we discuss emerging differences in the production and signaling of type I and type III IFNs, and summarize results of recent studies describing the involvement of type III IFNs in anti-bacterial and anti-fungal, as well as antiviral, defenses.

Indexed as

AnimalsBacterial InfectionsHumansImmunityInflammationInterferon LambdaInterferonsInterferon Type IMicrobiotaMycosesSignal TransductionVirus DiseasesInterferon LambdaInterferonsInterferon Type IAntiviral protectionEpithelial barrierImmune responseInterferonMicrobial infectionNeutrophils

Identifiers

PMID31771761
PMCPMC7141597
OpenAlexW2990634276

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.