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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=29904"><dc:title>Unraveling the role of IL-17 in lichen planus</dc:title><dc:creator>Tolušić Levak,	Maja	(Avtor)
	</dc:creator><dc:creator>Pauzar,	Mirta	(Avtor)
	</dc:creator><dc:creator>Plužarić,	Vera	(Avtor)
	</dc:creator><dc:creator>Francesch,	Nika	(Avtor)
	</dc:creator><dc:creator>Pauzar,	Biljana	(Avtor)
	</dc:creator><dc:creator>Rajc,	Jasmina	(Avtor)
	</dc:creator><dc:creator>Delaš Aždajić,	Marija	(Avtor)
	</dc:creator><dc:creator>Mihalj,	Martina	(Avtor)
	</dc:creator><dc:subject>inflammatory dermatoses</dc:subject><dc:subject>lichen planus</dc:subject><dc:subject>interleukin-17</dc:subject><dc:subject>immunoexpression</dc:subject><dc:description>Introduction: Lichen planus (LP) is a chronic T cell–mediated inflammatory disease affecting the skin and mucosa. Interleukin-17 (IL-17), a pro-inflammatory cytokine, has been implicated in LP pathogenesis, but its tissue-level expression across clinical variants remains underexplored. This study compares IL-17 expression in healthy skin and LP lesions and assesses variations based on clinical presentation. Methods: This cross-sectional retrospective study included 20 LP skin samples and 10 healthy controls. The sample collection spanned a period of 10 years. IL-17 expression was assessed via immunohistochemistry and quantified using a modified Q score. Samples were categorized by mucosal involvement and lesion distribution. Statistical analysis was performed with the MannWhitney U test. Results: IL-17 was absent in healthy skin but present in all LP samples. IL-17 expression was significantly higher in patients with both skin and oral mucosal involvement compared to those with cutaneous LP (p = 0.003). No significant difference was observed between generalized and localized LP. Conclusions: The results indicate a distinct increase in IL-17 expression in LP lesions, particularly with mucosal involvement, supporting its role in LP pathogenesis. These findings suggest IL-17 as a potential biomarker and therapeutic target, warranting further investigation in larger cohorts.</dc:description><dc:date>2025</dc:date><dc:date>2026-06-09 08:38:04</dc:date><dc:type>Neznano</dc:type><dc:identifier>29904</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
