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观察性研究表明,接受窄谱 UVB 治疗的瑞典斑块状银屑病患者皮损中 S100A8/A9 蛋白和基因表达水平降低,但对血清中 S100A8/A9 蛋白水平无影响。

Observational study on Swedish plaque psoriasis patients receiving narrowband-UVB treatment show decreased S100A8/A9 protein and gene expression levels in lesional psoriasis skin but no effect on S100A8/A9 protein levels in serum.

机构信息

Department of Dermatology and Venereology, Division of endocrinology, skin, reproductive health and ophthalmology, Skåne University Hospital, Malmö, Sweden.

Department of Clinical and Experimental Medicine, Faculty of Medicine and Health Sciences, Linköping University, Linköping, Sweden.

出版信息

PLoS One. 2019 Mar 13;14(3):e0213344. doi: 10.1371/journal.pone.0213344. eCollection 2019.

Abstract

S100A8 and S100A9 proteins are highly upregulated in patients with psoriasis and have been proposed as potential biomarkers for psoriasis. The present study was designed to analyze the effect of narrowband ultraviolet B therapy on these proteins. S100A8, S100A9 gene expression and S100A8/A9 heterocomplex protein levels were analyzed in lesional and non-lesional skin before and after narrowband-UVB treatment in patients with chronic plaque type psoriasis. In addition, disease severity was measured by psoriasis area and severity index (PASI) and serum protein levels of S100A8/A9 were repeatedly analyzed. Narrowband-UVB treatment significantly reduced S100A8, S100A9 gene expression and S100A8/A9 protein levels in lesional skin while serum levels showed no significant change. No correlation between PASI and serum S100A8/A9 protein levels was found. These results implicate a role of S100A8/A9 in the anti-inflammatory effect of narrowband-UVB. Serum S100A8/A9 levels do not respond to treatment suggesting that serum S100A8/A9 does not originate from psoriasis skin keratinocytes. Serum S100A8/A9 levels do not correlate with PASI questioning serum S100A8/A9 as a biomarker for psoriasis skin activity. Trial Registration: DRKS 00014817.

摘要

S100A8 和 S100A9 蛋白在银屑病患者中高度上调,并被提议作为银屑病的潜在生物标志物。本研究旨在分析窄带紫外线 B 治疗对这些蛋白的影响。在慢性斑块型银屑病患者接受窄带-UVB 治疗前后,分析了病变和非病变皮肤中的 S100A8、S100A9 基因表达和 S100A8/A9 异源复合物蛋白水平。此外,通过银屑病面积和严重程度指数(PASI)测量疾病严重程度,并反复分析 S100A8/A9 的血清蛋白水平。窄带-UVB 治疗显著降低了病变皮肤中的 S100A8、S100A9 基因表达和 S100A8/A9 蛋白水平,而血清水平没有显著变化。未发现 PASI 与血清 S100A8/A9 蛋白水平之间存在相关性。这些结果表明 S100A8/A9 参与了窄带-UVB 的抗炎作用。血清 S100A8/A9 水平对治疗无反应表明,血清 S100A8/A9 并非源自银屑病皮肤角质形成细胞。血清 S100A8/A9 水平与 PASI 无关,质疑血清 S100A8/A9 作为银屑病皮肤活性的生物标志物。

试验注册

DRKS 00014817。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d40/6415841/a521c71d1b3c/pone.0213344.g001.jpg

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