Evidence map›Paper›PMID 40721713›Full record

ArticleScientific reports2025

Clinical, histological, and immunohistochemical signatures of non-segmental vitiligo: A case-control analysis of Melan-A expression and CD8⁺ T-cell infiltration.

Melin Özgün Geçer, Gökhan Kaya

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Review
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

2 authors.

Melin Özgün GeçerDepartment of Pathology, Bezmialem Vakıf University, İstanbul, Türkiye.ORCID http://orcid.org/0000-0003-4849-0793
Gökhan KayaDepartment of Dermatology, Ministry of Health Nizip State Hospital, Gaziantep, Türkiye. gkhnkya@gmail.com.ORCID http://orcid.org/0000-0002-9651-4115

Funding

Bezmialem Scientific Research Projects Unit 20230908
6 · The paper itself

Abstract

Non-segmental vitiligo (NSV) is a chronic autoimmune skin disease marked by melanocyte loss and depigmented macules. While clinical features are well recognized, immunohistological correlates such as Melan-A expression and CD8⁺ T-cell infiltration remain undercharacterized. To examine the clinical, histological, and immunohistochemical features of NSV, with a focus on their relationship to disease severity. In this prospective case-control study, 25 NSV patients and 25 matched healthy controls were evaluated using standardized scoring systems (VASI, VIDA, VETF, VETI). Biopsies from lesional, marginal, and normal skin underwent immunohistochemical staining for Melan-A and CD8⁺ T cells. Histopathological changes were graded using a structured scoring system. Lesional skin exhibited significant melanocyte loss (Melan-A⁺ median: 5 [IQR: 3-8]) and elevated CD8⁺ T-cell infiltration (median: 15 [10-18]) compared to controls (p < 0.001). Marginal zones showed intermediate values, indicating subclinical immune activation. CD8⁺ infiltration positively correlated with VASI (r = 0.53), while Melan-A expression showed a negative correlation (r = - 0.55). Both markers were independent predictors of disease severity. NSV exhibits a spatial immunohistological gradient, where melanocyte loss and CD8⁺ T-cell infiltration parallel clinical severity. The integration of immunophenotyping with clinical scoring provides a novel biomarker strategy for personalized therapy.

Indexed as

CD8-Positive T-LymphocytesMART-1 AntigenVitiligoAdultCase-Control StudiesFemaleHumansImmunohistochemistryMaleMelanocytesMiddle AgedProspective StudiesSeverity of Illness IndexSkinYoung AdultMART-1 AntigenMLANA protein, humanCD8⁺ T cellsDisease severityImmunohistochemistryImmunophenotypingMelan-AVASIVIDAVitiligo

Identifiers

PMID40721713
PMCPMC12304201

What Socratic holds

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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 Socratic graph.