Notable Differences in Clinical Features and Inflammatory Gene Expression Between Genital Lichen Sclerosus and Lichen Planus
<b>Background/Objectives</b>: Genital lichen sclerosus (LS) and lichen planus genitalis (Lpg) are chronic inflammatory dermatoses with overlapping clinical features but incompletely understood pathogenesis. Current therapies are largely symptomatic. <b>Methods</b>: To clarify underlying mechanisms and identify therapeutic targets, we retrospectively analyzed 174 patients (142 LS and 32 Lpg). Clinical features and comorbidities were compared, and gene expression profiling of 730 inflammation-related genes was performed on lesional tissue from LS and Lpg patients and healthy controls using NanoString technology. Selected findings were validated by immunohistochemistry. <b>Results</b>: LS patients were older and predominantly female and more frequently had metabolic syndrome. On the molecular level, LS showed a generally lower inflammatory gene expression profile than Lpg. Nevertheless, LS was characterized by strong upregulation of CCL27 and MARCO, whereas Lpg displayed enhanced IL-1 pathway activation and increased expression of B-cell-associated markers. <b>Conclusions</b>: These results demonstrate distinct immunological differences between the two conditions and provide further insight into disease-specific pathways.
Authors
- Barbara Meier (ORCID: https://orcid.org/0000-0003-2807-5066)
- Irina Banzola (ORCID: https://orcid.org/0000-0002-5600-7688)
- Fabienne Fröhlich (ORCID: https://orcid.org/0000-0002-2999-6388)
- Mark Mellett (ORCID: https://orcid.org/0000-0002-6315-167X)
- Veronika Baghin
- Lucie Heinzerling
- Julia Laube
- Patrick Poffet (ORCID: https://orcid.org/0009-0001-1239-6052)
Institutions
- LMU Klinikum (DE)
- University Hospital of Zurich (CH)
- Ludwig-Maximilians-Universität München (DE)
Publication Details
- Journal
- Biomedicines
- Published
- 2025-11-19
- DOI
- https://doi.org/10.3390/biomedicines13112817
- Primary Topic
- Genital Health and Disease
- Type
- article
- Field-Weighted Citation Impact
- 0.00