Evidence map›Paper›PMID 38686385›Full record

ReviewFrontiers in immunology2024

IL-23 past, present, and future: a roadmap to advancing IL-23 science and therapy.

James G Krueger, Kilian Eyerich, Vijay K Kuchroo, Christopher T Ritchlin, Maria T Abreu, M Merle Elloso, Anne Fourie, Steven Fakharzadeh, Jonathan P Sherlock, Ya-Wen Yang and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

78 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. The role of IL-17 and Th17 cells in keloid pathogenesis.Archives of dermatological research · 2024
    Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. [Psoriatic arthritis].Innere Medizin (Heidelberg, Germany) · 2026
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. New and emerging therapies in type 1 diabetes mellitus.The Journal of clinical investigation · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

18 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

12 authors.

James G KruegerLaboratory for Investigative Dermatology, The Rockefeller University, New York, NY, United States.
Kilian EyerichDepartment of Medicine, Division of Dermatology and Venereology, Karolinska Institute, Stockholm, Sweden.
Vijay K KuchrooEvergrande Center for Immunologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Christopher T RitchlinAllergy, Immunology & Rheumatology Division, Center for Musculoskeletal Research, University of Rochester Medical School, Rochester, NY, United States.
Maria T AbreuDivision of Gastroenterology, Department of Medicine, University of Miami Leonard Miller School of Medicine, Miami, FL, United States.
M Merle EllosoJanssen Scientific Affairs, LLC, Horsham, PA, United States.
Anne FourieJanssen Research & Development, LLC, San Diego, CA, United States.
Steven FakharzadehImmunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson, Horsham, PA, United States.
Jonathan P SherlockJanssen Research & Development, LLC, Spring House, PA, United States.
Ya-Wen YangImmunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson, Horsham, PA, United States.
Daniel J CuaJanssen Research & Development, LLC, Spring House, PA, United States.
Iain B McInnesCollege of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-23, an IL-12 cytokine family member, is a hierarchically dominant regulatory cytokine in a cluster of immune-mediated inflammatory diseases (IMIDs), including psoriasis, psoriatic arthritis, and inflammatory bowel disease. We review IL-23 biology, IL-23 signaling in IMIDs, and the effect of IL-23 inhibition in treating these diseases. We propose studies to advance IL-23 biology and unravel differences in response to anti-IL-23 therapy. Experimental evidence generated from these investigations could establish a novel molecular ontology centered around IL-23-driven diseases, improve upon current approaches to treating IMIDs with IL-23 inhibition, and ultimately facilitate optimal identification of patients and, thereby, outcomes.

Indexed as

Interleukin-23AnimalsArthritis, PsoriaticHumansInflammatory Bowel DiseasesPsoriasisSignal TransductionInterleukin-23cytokineIL-23immune-mediated inflammatory diseasesinflammatory bowel diseasepsoriasispsoriatic arthritis

Identifiers

PMID38686385
PMCPMC11056518

What Socratic 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 Socratic graph.