Garzorz Natalie, Eyerich Kilian
Department of Dermatology and Allergy, Technische Universität Munich, Munich, Germany.
Expert Rev Clin Immunol. 2015 Feb;11(2):167-9. doi: 10.1586/1744666X.2015.996549. Epub 2014 Dec 25.
Chronic inflammatory skin diseases such as psoriasis and eczema are a major medical challenge. Development of highly specific therapies for both conditions is opposed by the lack of translation of basic knowledge into biomarkers for clinical use. Furthermore, to distinguish psoriasis from eczema might be difficult occasionally, but specific and costly therapies would not be efficient in misdiagnosed patients. In the era of high-throughput 'omics'-technologies, comparing the molecular signature of psoriasis and eczema is a promising approach to gain insight into their complex pathogeneses and develop new diagnostic and therapeutic strategies. Investigating patients affected by both psoriasis and eczema simultaneously, we recently constructed a disease classifier consisting of only two genes (NOS2 and CCL27) that reliably predicts the correct diagnosis even in clinically unclear cases. When such easy-to-handle approaches are combined with individual therapeutic response, we might reach the ultimate goal of personalized medicine in inflammatory skin diseases in near future.
银屑病和湿疹等慢性炎症性皮肤病是一项重大的医学挑战。由于缺乏将基础知识转化为临床可用生物标志物的能力,这两种疾病的高度特异性疗法的开发受到阻碍。此外,偶尔区分银屑病和湿疹可能很困难,但针对误诊患者使用特定且昂贵的疗法可能无效。在高通量“组学”技术时代,比较银屑病和湿疹的分子特征是深入了解其复杂发病机制并开发新诊断和治疗策略的一种有前景的方法。我们最近通过同时研究受银屑病和湿疹影响的患者,构建了一个仅由两个基因(NOS2和CCL27)组成的疾病分类器,即使在临床情况不明确的病例中也能可靠地预测正确诊断。当这种易于操作的方法与个体治疗反应相结合时,我们可能在不久的将来实现炎症性皮肤病个性化医疗的最终目标。