Evidence map›Paper›PMID 33193342›Full record

ReviewFrontiers in immunology2020

Autoimmunity in Segmental Vitiligo.

Reinhart Speeckaert, Jo Lambert, Vedrana Bulat, Arno Belpaire, Marijn Speeckaert, Nanja van Geel

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Guideline
  2. Demographic factors associated with response to topical Jak inhibitors in a diverse vitiligo cohort.JID innovations : skin science from molecules to population health · 2026
    Article
  3. Review
  4. Vitiligo.Nature reviews. Disease primers · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Vitiligo: From Pathogenesis to Treatment.Journal of clinical medicine · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 2 countries.

Reinhart SpeeckaertDepartment of Dermatology, Gent University Hospital, Gent, Belgium.
Jo LambertDepartment of Dermatology, Gent University Hospital, Gent, Belgium.
Vedrana BulatDepartment of Dermatology, University Hospital Centre Zagreb, Zagreb, Croatia.
Arno BelpaireDepartment of Dermatology, Gent University Hospital, Gent, Belgium.
Marijn SpeeckaertDepartment of Nephrology, Gent University Hospital, Gent, Belgium.
Nanja van GeelDepartment of Dermatology, Gent University Hospital, Gent, Belgium.
Ghent University Hospital · BEUniversity Hospital Centre Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The autoimmune basis of segmental vitiligo (SV) has only recently been recognized. Systemic autoimmune diseases are less frequently associated compared to non-segmental vitiligo (NSV), but localized skin disorders - in particular linear morphea - have been repeatedly observed in patients with SV. The inflammatory response is documented on a clinical level with cases displaying erythematous borders or a hypochromic stage, on a histopathological level with predominantly CD8 lymphocytes migrating toward the basal layer and by flow cytometry demonstrating the antimelanocyte specificity of these cytotoxic T cells. The increased risk for halo naevi and NSV in these patients further underline the immune-mediated mechanisms of SV. Nonetheless, the localized and unique distribution pattern points to somatic mosaicism. This places SV in a category of similar diseases such as lichen striatus, blaschkitis, linear lupus erythematosus, and linear scleroderma where an immune reaction against genetically mutated skin cells is believed to be the underlying cause. All these disorders are characterized by a young age of onset, a temporary disease activity with spontaneous resolution, limited response to treatment, and often long-term sequelae. Although challenging, genetic research proving this genetic mosaicism could offer crucial insights into the pathogenesis of both segmental and non-segmental vitiligo.

Indexed as

AutoimmunityAnimalsHumansMosaicismVitiligoimmunologylichen striatuslinear morpheamosaicismsegmental vitiligo

Identifiers

PMID33193342
PMCPMC7655129
OpenAlexW3095612328

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.