Evidence map›Paper›PMID 25516297›Full record

ReviewCytokine2015

IL12Rβ1: the cytokine receptor that we used to know.

Richard T Robinson

Open access · greenAbstract readReview
In one paragraph

Review in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

40 citing papers in PubMed, 62 citations in OpenAlex.

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

1 author at 1 institution in 1 country.

Richard T RobinsonDepartment of Microbiology and Molecular Genetics, The Medical College of Wisconsin, Milwaukee, WI 53226, United States. Electronic address: rrobinson@mcw.edu.
Medical College of Wisconsin · US

Funding

M.tuberculosis-induced Alternative Processing of IL12RB1 mRNAR21AI099661 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI MCNALLY, MARK T, ROBINSON, RICHARD · 2013 to 2014
$421k
NIAID NIH HHS R21 AI099661NIAID NIH HHS R21AI099661
6 · The paper itself

Abstract

Human IL12RB1 encodes IL12Rβ1, a type I transmembrane receptor that is an essential component of the IL12- and IL23-signaling complex. IL12RB1 is well-established as being a promoter of delayed type hypersensitivity (DTH), the immunological reaction that limits tuberculosis. However, recent data demonstrate that in addition to promoting DTH, IL12RB1 also promotes autoimmunity. The contradictory roles of IL12RB1 in human health raises the question, what are the factors governing IL12RB1 function in a given individual, and how is inter-individual variability in IL12RB1 function introduced? Here we review recent data that demonstrate individual variability in IL12RB1 function is introduced at the epigenetic, genomic polymorphism, and mRNA splicing levels. Where and how these differences contribute to disease susceptibility and outcome are also reviewed. Collectively, recent data support a model wherein IL12RB1 sequence variability - whether introduced at the genomic or post-transcriptional level - contributes to disease, and that human IL12RB1 is not as simple a gene as we once believed.

Indexed as

Alternative SplicingAnimalsAsthmaBacterial InfectionsEpigenesis, GeneticExonsGenomicsHumansInterleukin-12Interleukin-12 Receptor beta 1 SubunitInterleukin-23MiceModels, GeneticNeoplasmsPhylogenyRNA, MessengerInterleukin-12Interleukin-12 Receptor beta 1 SubunitInterleukin-23RNA, Messengeril12rb1Interleukin-12Interleukin-23SplicingTuberculosis

Identifiers

PMID25516297
PMCPMC4346141
OpenAlexW1995711064

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.