Evidence map›Paper›PMID 14981113›Full record

ArticleThe Journal of experimental medicine2004

Spontaneous development of psoriasis in a new animal model shows an essential role for resident T cells and tumor necrosis factor-alpha.

Onur Boyman, Hans Peter Hefti, Curdin Conrad, Brian J Nickoloff, Mark Suter, Frank O Nestle

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 194 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
194citing papers in PubMed, 1 pooled it
12.0field-weighted citation impact, top 1% 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

194 citing papers in PubMed, 1 synthesis or guideline pooled it, 511 citations in OpenAlex.

  1. Pooled it
  2. The PKC inhibitor AEB071 may be a therapeutic option for psoriasis.The Journal of clinical investigation · 2008
    Trial
  3. Alefacept reduces infiltrating T cells, activated dendritic cells, and inflammatory genes in psoriasis vulgaris.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Trial
  4. Article
  5. Review
  6. Hidden immune memory niches in inflammatory skin diseases.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Evolving role of CD8Frontiers in immunology · 2026
    Review
  11. Article
  12. Article
  13. CD4Immunology and cell biology · 2025
    Review
  14. Article
  15. Cutaneous T cell immunity.Nature immunology · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

134 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

6 authors at 3 institutions in 2 countries.

Onur BoymanDepartment of Dermatology, University Hospital of Zurich, Gloriastrasse 31, CH-8091, Switzerland.
Hans Peter Hefti
Curdin Conrad
Brian J Nickoloff
Mark Suter
Frank O Nestle
University Hospital of Zurich · CHLoyola University Medical Center · USUniversity of Zurich · CH

Funding

ROLE OF ADHESION MOLECULES IM PSORIASISR01AR040065 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NICKOLOFF, BRIAN J · 1989 to 2009
$2.7M
PHENOTYPE AND FUNCTION OF SENESCENT KERATINOCYTESR01AR047307 · NIAMS · LOYOLA UNIVERSITY CHICAGO · PI NICKOLOFF, BRIAN J · 2001 to 2005
$1.8M
NIAMS NIH HHS AR40065NIAMS NIH HHS AR47307NIAMS NIH HHS R01 AR040065NIAMS NIH HHS R01 AR047307
6 · The paper itself

Abstract

Psoriasis is a common T cell-mediated autoimmune disorder where primary onset of skin lesions is followed by chronic relapses. Progress in defining the mechanism for initiation of pathological events has been hampered by the lack of a relevant experimental model in which psoriasis develops spontaneously. We present a new animal model in which skin lesions spontaneously developed when symptomless prepsoriatic human skin was engrafted onto AGR129 mice, deficient in type I and type II interferon receptors and for the recombination activating gene 2. Upon engraftment, resident human T cells in prepsoriatic skin underwent local proliferation. T cell proliferation was crucial for development of a psoriatic phenotype because blocking of T cells led to inhibition of psoriasis development. Tumor necrosis factor-alpha was a key regulator of local T cell proliferation and subsequent disease development. Our observations highlight the importance of resident T cells in the context of lesional tumor necrosis factor-alpha production during development of a psoriatic lesion. These findings underline the importance of resident immune cells in psoriasis and will have implications for new therapeutic strategies for psoriasis and other T cell-mediated diseases.

Indexed as

AnimalsCell DivisionDisease Models, AnimalDNA-Binding ProteinsHumansMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutNuclear ProteinsPhenotypePsoriasisReceptor, Interferon alpha-betaReceptors, InterferonSkin TransplantationT-LymphocytesDNA-Binding Proteinsinterferon receptor, type IIMembrane ProteinsNuclear ProteinsRAG2 protein, humanRag2 protein, mouseReceptor, Interferon alpha-betaReceptors, InterferonTumor Necrosis Factor-alphaV(D)J recombination activating protein 2

Identifiers

PMID14981113
PMCPMC2213300
OpenAlexW2129016683

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.