Evidence map›Paper›PMID 39978685›Full record

ArticleThe Journal of allergy and clinical immunology2025

Psoriasis harbors multiple pathogenic type 17 T-cell subsets: Selective modulation by risankizumab.

Jaehwan Kim, Jongmi Lee, Jongeun Lee, Katherine Kim, Xuan Li, Wei Zhou, Junyue Cao, James G Krueger

Registry-linked trialAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04630652 (Immune Modification of Psoriasis by Selective IL-23 Blockade Using Risankizumab), which is not on this map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing 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.

NCT04630652 phase4completednot on this map

Immune Modification of Psoriasis by Selective IL-23 Blockade Using Risankizumab

TypeinterventionalSponsorJaehwan KimRan2021 to 2025Enrolled24ConditionsPsoriasisArmsRisankizumab-Rzaa, Punch biopsies of the skin at baseline visit, Punch biopsies of the skin at week 28 visit
3 · Its place in the literature

Who cites it

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

  1. Pooled it
  2. Review
  3. Article
  4. Melittin attenuates imiquimod-induced psoriatic dermatitis in mice: a role for autophagy activation via PI3K/Akt/mTOR pathway suppression.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Keratinocytes: pleiotropic orchestrators of cutaneous immunity and Inflammation - Emerging therapeutic paradigms in dermatological pathologies.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. A review of core immuno-inflammatory mechanisms and key regulatory targets in psoriasis.American journal of clinical and experimental immunology · 2026
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Relative Fat Mass and Psoriasis Risk: Evidence from NHANES 2009-2014.Journal of multidisciplinary healthcare · 2025
    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

8 authors.

Jaehwan KimDepartment of Dermatology, University of California, Davis, Sacramento, Calif; Dermatology Section, Veterans Affairs Northern California Health Care System, Mather, Calif; Laboratory for Investigative Dermatology, The Rockefeller University, New York, NY. Electronic address: derkim@ucdavis.edu.
Jongmi LeeDepartment of Dermatology, University of California, Davis, Sacramento, Calif; Dermatology Section, Veterans Affairs Northern California Health Care System, Mather, Calif.
Jongeun LeeLaboratory for Investigative Dermatology, The Rockefeller University, New York, NY.
Katherine KimDepartment of Dermatology, University of California, Davis, Sacramento, Calif; Dermatology Section, Veterans Affairs Northern California Health Care System, Mather, Calif.
Xuan LiLaboratory for Investigative Dermatology, The Rockefeller University, New York, NY.
Wei ZhouLaboratory of Single-cell Genomics and Population Dynamics, The Rockefeller University, New York, NY.
Junyue CaoLaboratory of Single-cell Genomics and Population Dynamics, The Rockefeller University, New York, NY.
James G KruegerLaboratory for Investigative Dermatology, The Rockefeller University, New York, NY. Electronic address: kruegej@mail.rockefeller.edu.

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
A clinical trial for psoriasis with novel single-cell genomic techniques to understand regulatory immunity behind long-term disease remission off drug induced by short-term IL-23 inhibitionK23AR080043 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Jaehwan Kim · 2022 to 2026
$846k
NCATS NIH HHS UL1 TR001866NIAMS NIH HHS K23 AR080043
6 · The paper itself

Abstract

backgroundRecent single-cell studies indicated that IL-17-producing T cells (T17) have diverse subsets expressing IL-17A, IL-17F, or a combination in human psoriasis skin. However, it is unknown how T17 subsets are differently regulated by IL-23 versus IL-17A blockade.

objectiveWe sought to investigate how systemic monoclonal antibody injections blocking IL-23 versus IL-17A differently modify immune cell transcriptomes in human psoriasis skin.

methodsWe analyzed a total of 93 human skin single-cell libraries, including 42 psoriasis pretreatment lesional skin, 25 psoriasis pretreatment nonlesional skin, 12 psoriasis posttreatment after IL-23 inhibition, 4 psoriasis posttreatment after IL-17A inhibition, and 10 control skin samples. CLINICALTRIALS: gov NCT04630652.

resultsOf the six T17 subsets identified, an IL17A

conclusionsThis study suggests multiple immune mechanisms of how IL-23 inhibition can modify the complex inflammatory environment present in psoriatic skin, highlighting the roles of specific T17 subsets in psoriasis development and background skin protection.

Indexed as

Antibodies, MonoclonalPsoriasisTh17 CellsT-Lymphocyte SubsetsAdultFemaleHumansInterleukin-17Interleukin-23MaleMiddle AgedSkinAntibodies, MonoclonalIL17A protein, humanInterleukin-17Interleukin-23risankizumabdendritic cellIL-17AIL-17FIL-23keratinocytemyeloid cellPsoriasissingle-cell RNA sequencingT celltype 17 T cells

Identifiers

PMID39978685
PMCPMC12145251

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.