Evidence map›Paper›PMID 8878440›Full record

ArticleThe Journal of clinical investigation1996

Dermal injection of immunocytes induces psoriasis.

T Wrone-Smith, B J Nickoloff

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

90 citing papers in PubMed, 436 citations in OpenAlex.

  1. 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
  2. Trial
  3. Trial
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  5. Trial
  6. Article
  7. Article
  8. Article
  9. Review
  10. Effect of Systemic Administration of CD4Comparative medicine · 2023
    Article
  11. Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Mouse Models of Psoriasis: A Comprehensive Review.The Journal of investigative dermatology · 2022
    Review
  14. Antimicrobial Peptides: A New Hope in Biomedical and Pharmaceutical Fields.Frontiers in cellular and infection microbiology · 2021
    Review
  15. Role of Innate Immune Cells in Psoriasis.International journal of molecular sciences · 2020
    Review
  16. Review
  17. Toxins · 2019
    Review
  18. Review
  19. Article
  20. Review

30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

T Wrone-SmithDepartment of Pathology, University of Michigan, Ann Arbor 48104, USA.
B J Nickoloff
University of Michigan–Ann Arbor · US

Funding

ROLE OF ADHESION MOLECULES IM PSORIASISR01AR040065 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NICKOLOFF, BRIAN J · 1989 to 2009
$2.7M
DERMAL DENDROCYTES AND AIDS-RELATED PSORIASISR01AR040488 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NICKOLOFF, BRIAN J · 1991 to 1993
–
INTERACTION OF GAMMA INTERFERON WITH KERATINOCYTESR29AR038957 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NICKOLOFF, BRIAN J · 1987 to 1989
–
NIAMS NIH HHS AR38957NIAMS NIH HHS AR40065NIAMS NIH HHS AR40488
6 · The paper itself

Abstract

Establishing direct and causal relationships among the confederacy of activated cell types present in psoriasis has been hampered by lack of an animal model. Within psoriatic plaques there are hyperplastic keratinocytes, infiltrating immunocytes, and activated endothelial cells. The purpose of this study was to determine if psoriasis is primarily a disorder of keratinocytes or the immune system. Using a newly developed experimental system in which full-thickness human skin is orthotopically transferred onto severe combined immunodeficient mice, autologous immunocytes were injected into dermis, and the resultant phenotype characterized by clinical, histologic, and immunophenotypic analyses. Engraftment of samples included both uninvolved/ symptomless (PN) skin removed from patients with psoriasis elsewhere, or from healthy individuals with no skin disease (NN skin). In 10 different experiments involving 6 different psoriasis patients, every PN skin was converted to a full-fledged psoriatic plaque skin by injection of autologous blood-derived immunocytes. In all but one psoriatic patient, the immunocytes required preactivation with IL-2 and superantigens to convert PN skin into psoriatic plaque skin. In every case, resultant plaques were characterized by visible presence of flaking and thickened skin, loss of the granular cell layer, prominent elongation of rete pegs with a dermal angiogenic tissue reaction, and infiltration within the epidermis by T cells. Lesional skin displayed 20 different antigenic determinants of the psoriatic phenotype. None of the four NN skin samples injected with autologous immunocytes converted to psoriatic plaques. We conclude that psoriasis is caused primarily by the ability of pathogenetic blood-derived immunocytes to induce secondary activation and disordered growth of endogenous cutaneous cells including keratinocytes and vascular endothelium.

Indexed as

AdultAgedAnimalsFemaleHLA-DR AntigensHumansImmunohistochemistryKeratinocytesMaleMiceMice, SCIDMiddle AgedProliferating Cell Nuclear AntigenPsoriasisSkinSkin TransplantationHLA-DR AntigensProliferating Cell Nuclear Antigen

Identifiers

PMID8878440
PMCPMC507628
OpenAlexW2090306216

What OpenQuestion holds

Textmetadata
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.