Evidence map›Paper›PMID 41711590›Full record

ArticleJournal of lower genital tract disease2026

Multiomics Analysis Reveals Distinct Changes in the Cellular Composition of Vulvar Lichen Sclerosus.

Xiaoyi Sun, Cenxi Liu, Yixin Sun, Xinyi Chen, Qing Cong, Jin Li

Abstract read
In one paragraph

Article in Journal of lower genital tract disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Xiaoyi SunObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.
Cenxi LiuObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.
Yixin SunObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.
Xinyi ChenObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.
Qing CongObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.
Jin LiObstetrics & Gynecology Hospital, State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate cellular composition and gene/pathway alterations in VLS tissue compared with normal skin using single-cell RNA sequencing (scRNA-seq) and lipid metabolomics.

methodsscRNA-seq was conducted on 4 VLS samples and self-control vulvar skin. Lipid metabolism analysis was performed on 15 VLS samples. Bioinformatics assessed cellular abundance, differentially expressed genes (DEGs), and functional pathways between VLS and normal tissues. DEGs were validated via immunofluorescence.

resultsThe authors found significant changes in cell-type abundance in the LS samples, with increased abundance of T cells, particularly the C01-GZMB/GZMK and C05-GNLY/XCL1 T cell subsets, and decreased abundance of fibroblasts, keratinocytes, and melanocytes. Furthermore, scRNA-seq data indicated distinct trends in the expression of key metabolic and inflammatory genes. Notably, lymphocyte-mediated immunity, leukocyte-mediated cytotoxicity, and cell-killing pathways were upregulated in the T cells of VLS, suggesting an ongoing inflammatory milieu. Cell communication analysis revealed an increase in the interactions among cell types, with the interaction intensity between T cells and fibroblasts showing the most pronounced increase. Immunofluorescence results revealed that GZMB and the pro-inflammatory factors, IFN-γ and TNF-β, were significantly increased in the VLS tissues. The epidermal keratin expression in the VLS tissue was abnormal, and the basal layer of the VLS tissue lost its normal single-layer structure, and the arrangement was disordered.

conclusionCellular composition changes in VLS T cells lead to apoptosis of normal skin cells, contributing to skin tissue destruction and playing a critical role in the inflammatory development of the disease.

Indexed as

Vulvar Lichen SclerosusFemaleGene Expression ProfilingHumansLipid MetabolismMultiomicsSingle-Cell AnalysisSingle-Cell Gene Expression AnalysisSkinimmune cellslichen sclerosusRNA sequencingsingle-cell sequencing

Identifiers

PMID41711590
PMCPMC12994910

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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 OpenQuestion graph.