Evidence map›Paper›PMID 24945094›Full record

ArticleThe Journal of investigative dermatology2014

The IL-17A-producing CD8+ T-cell population in psoriatic lesional skin comprises mucosa-associated invariant T cells and conventional T cells.

Marcel B M Teunissen, Nataliya G Yeremenko, Dominique L P Baeten, Saskia Chielie, Phyllis I Spuls, Menno A de Rie, Olivier Lantz, Pieter C M Res

Open access · bronzeAbstract read
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In one paragraph

Article in The Journal of investigative dermatology, 2014. 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
5.7field-weighted citation impact, top 3% 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, 157 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. CD4Frontiers in immunology · 2026
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  7. Review
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  9. Circulating CLAJID innovations : skin science from molecules to population health · 2025
    Review
  10. Cytotoxic T Cells: Kill, Memorize, and Mask to Maintain Immune Homeostasis.International journal of molecular sciences · 2025
    Review
  11. Epidermal and Dermal T Cells Exhibit Distinct Proteomic Signatures.International journal of molecular sciences · 2025
    Article
  12. Cladribine Ameliorates Imiquimod Induced Murine Psoriasiform Dermatitis.Clinical, cosmetic and investigational dermatology · 2025
    Article
  13. Persistent reduction ofFrontiers in immunology · 2025
    Article
  14. Article
  15. Article
  16. The Immunology of Psoriasis-Current Concepts in Pathogenesis.Clinical reviews in allergy & immunology · 2024
    Review
  17. Investigating Vα7.2International journal of molecular sciences · 2024
    Article
  18. Article
  19. IL-4-secreting CD40LInflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    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

8 authors at 3 institutions in 2 countries.

Marcel B M TeunissenDepartment of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands. Electronic address: m.b.teunissen@amc.uva.nl.
Nataliya G YeremenkoDepartment of Clinical Immunology and Rheumatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Dominique L P BaetenDepartment of Clinical Immunology and Rheumatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Saskia ChielieDepartment of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Phyllis I SpulsDepartment of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Menno A de RieDepartment of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Olivier LantzInstitut Curie, Département de Biologie des Tumeurs, Paris, France.
Pieter C M ResDepartment of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Amsterdam UMC Location University of Amsterdam · NLInstitut Curie · FRUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IL-17A is pivotal in the etiology of psoriasis, and CD8(+) T cells with the ability to produce this cytokine (Tc17 cells) are over-represented in psoriatic lesions. Here we demonstrate that the frequency of Tc17 cells in peripheral blood of psoriasis patients correlated with the clinical severity of the disease. Analysis of cutaneous-associated lymphocyte antigen expression showed that the blood Tc17 population contains a significantly higher proportion of cells with skin-homing potential compared with the CD8(+) T-cell population lacking IL-17A/IL-22 expression. IL-17A-producing CD8(+) T cells in blood have previously been reported to belong mainly to the mucosa-associated invariant T-cell (MAIT cell) lineage characterized by TCR Vα7.2 chain, CD161, IL-18Rα, and multidrug transporter ABCB1 expression. We demonstrate the presence of CD8(+) MAIT cells in the dermis and epidermis of psoriatic plaques, as well as healthy skin; however, IL-17A-producing CD8(+) MAIT cells were predominantly found in psoriatic skin. Notably, we observed IL-17A production in a large proportion of psoriatic plaque-derived CD8(+) T cells devoid of MAIT cell characteristics, likely representing conventional CD8(+) T cells. In conclusion, we provide supporting evidence that implicates Tc17 cells in the pathogenesis of psoriasis and describe the presence of innate CD8(+) MAIT cells in psoriatic lesions as an alternative source of IL-17A.

Indexed as

AdultAgedCase-Control StudiesCD8-Positive T-LymphocytesCell CountFemaleHumansInterferon-gammaInterleukin-17Interleukin-22InterleukinsMaleMiddle AgedMucous MembranePsoriasisRetrospective StudiesInterferon-gammaInterleukin-17Interleukin-22Interleukins

Identifiers

PMID24945094
OpenAlexW2088836758

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.