Evidence map›Paper›PMID 32012221›Full record

ArticleThe British journal of dermatology2020

Phenotype and function of circulating memory T cells in human vitiligo.

C Martins, A-S Darrigade, C Jacquemin, T Barnetche, A Taieb, K Ezzedine, K Boniface, J Seneschal

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In one paragraph

Article in The British journal of dermatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Vitiligo.Nature reviews. Disease primers · 2025
    Review
  6. Circulating CLAJID innovations : skin science from molecules to population health · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Circulating memory T cells and TCF1Journal of pharmaceutical analysis · 2024
    Article
  12. Article
  13. Aetiopathogenesis of Vitiligo.Dermatology practical & conceptual · 2023
    Review
  14. Review
  15. Altered circulating memory T cells in vitiligo cases followed NB-UVB therapy.Photodermatology, photoimmunology & photomedicine · 2022
    Article
  16. Review
  17. Article
  18. Human CLAFrontiers in medicine · 2021
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

C MartinsINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.ORCID 0000-0002-9160-1017
A-S DarrigadeINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.ORCID 0000-0003-4034-0395
C JacqueminINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.ORCID 0000-0003-1617-5959
T BarnetcheDepartment of Rheumatology, National Reference Center for Severe Systemic Auto-Immune Diseases, Hôpital Pellegrin, CHU de Bordeaux, Bordeaux, France.
A TaiebINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.
K EzzedineDepartment of Dermatology, AP-HP, Hôpital Henri-Mondor, Créteil, France.ORCID 0000-0002-5468-4589
K BonifaceINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.ORCID 0000-0003-4428-1222
J SeneschalINSERM U1035, BMGIC, Immuno-Dermatology Team, University of Bordeaux, Bordeaux, France.ORCID 0000-0003-1139-0908
Université de Bordeaux · FRCentre Hospitalier Universitaire de Bordeaux · FRHôpitaux Universitaires Henri-Mondor · FR

Funding

Agence Nationale de la RechercheATIP-AVENIR
6 · The paper itself

Abstract

backgroundVitiligo is a chronic inflammatory skin disorder characterized by the loss of melanocytes. While a T helper cell (Th)1/cytotoxic T cell (Tc)1-skewed immune response is now well demonstrated in vitiligo, recent data suggest that the T-cell component could be more complex, involving different combinatorial T-cell subsets.

objectivesTo analyse the phenotype and function of circulating CD4

methodsThis is a monocentric, prospective, descriptive and exploratory study. Multiparametric flow cytometry analyses were performed to evaluate the surface expression of homing and T-cell-subset markers together with intracellular cytokine production in peripheral blood mononuclear cells from 60 patients with vitiligo, 25 patients with psoriasis and 28 healthy donors.

resultsVitiligo peripheral blood circulating effector and central memory T cells expressed similar proportions of skin-homing markers. Decrease in the frequencies of circulating CD4

conclusionsThe decreased frequencies of circulating Th1/Tc1, Th17/Tc17 and Th1/Th17-Tc1/Tc17 cells suggest a possible migration of these T-cell subsets into the skin of patients with vitiligo. These could be targeted to prevent flares of the disease. What is already known about this topic? Vitiligo is a chronic inflammatory skin disorder associated with the loss of melanocytes. Vitiligo is characterized by a T helper cell (Th)1/cytotoxic T cell (Tc)1-skewed immune response in the skin. What does this study add? A thorough analysis of the phenotype and function of circulating memory T cells suggests the migration of Th1/Tc1, Th17/Tc17 and Th1/Th17-Tc1/Tc17 cell subsets in the skin. What is the translational message? A better understanding of the different immune T-cell subsets involved in vitiligo could lead to better therapeutic options. Linked Comment: Matos. Br J Dermatol 2020; 183:803.

Indexed as

VitiligoCD8-Positive T-LymphocytesHumansImmunologic MemoryLeukocytes, MononuclearPhenotypeProspective StudiesTh17 CellsTh1 CellsT-Lymphocyte Subsets

Identifiers

PMID32012221
OpenAlexW3004476104

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.