Evidence map›Paper›PMID 25222143›Full record

ReviewCurrent opinion in chemical biology2014

Small-molecule control of cytokine function: new opportunities for treating immune disorders.

Thomas B Sundberg, Ramnik J Xavier, Stuart L Schreiber, Alykhan F Shamji

Open access · hybridAbstract readReview
In one paragraph

Review in Current opinion in chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Interleukin-36: Structure, Signaling and Function.Advances in experimental medicine and biology · 2021
    Review
  6. Identification of a HumanFrontiers in immunology · 2020
    Article
  7. Article
  8. Article
  9. Review
  10. Protein kinase CK2 governs the molecular decision between encephalitogenic TH17 cell and Treg cell development.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  11. Review
  12. 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

4 authors at 2 institutions in 1 country.

Thomas B SundbergCenter for the Science of Therapeutics, Broad Institute, Cambridge, MA 02142, USA.
Ramnik J XavierProgram in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA; Gastrointestinal Unit and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital, Boston, MA 02114, USA; Center for Computational and Integrative Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Stuart L SchreiberCenter for the Science of Therapeutics, Broad Institute, Cambridge, MA 02142, USA; Howard Hughes Medical Institute, USA; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Alykhan F ShamjiCenter for the Science of Therapeutics, Broad Institute, Cambridge, MA 02142, USA. Electronic address: ashamji@broadinstitute.org.
Broad Institute · USMassachusetts General Hospital · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Howard Hughes Medical InstituteNIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Manipulating cytokine function with protein-based drugs has proven effective for treating a wide variety of autoimmune and autoinflammatory disorders. However, the limited ability of protein-based drugs to modulate intracellular targets, including many implicated by studies of the genetics and physiology of these diseases, and to coordinately neutralize redundant inflammatory cytokines, suggests an important and complementary role for small molecules in immunomodulatory drug development. The recent clinical approval of Janus kinase and phosphodiesterase inhibitors, along with emerging evidence from other compound classes, firmly establish small molecules as effective tools for modulating therapeutically relevant proteins that give rise to aberrant cytokine signaling or mediate its downstream consequences.

Indexed as

AnimalsAutoimmune DiseasesCytokinesDrug DiscoveryHumansImmunologic FactorsSmall Molecule LibrariesCytokinesImmunologic FactorsSmall Molecule Libraries

Identifiers

PMID25222143
PMCPMC5087273
OpenAlexW2077000732

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.