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皮肤胶带撕脱法鉴定与变应性接触性皮炎相关的基因转录特征。

Skin tape stripping identifies gene transcript signature associated with allergic contact dermatitis.

机构信息

Tufts University School of Medicine, Boston, Massachusetts, US.

Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, US.

出版信息

Contact Dermatitis. 2021 May;84(5):308-316. doi: 10.1111/cod.13749. Epub 2020 Dec 21.

Abstract

BACKGROUND

Allergic contact dermatitis (ACD) and irritant contact dermatitis (ICD) are common skin conditions with an overlapping clinical and histological appearance, but distinct underlying mechanisms. Patch testing is the gold standard for ACD diagnosis, yet the interpretation of its results may be confounded by weak and varying macroscopic reactions.

OBJECTIVE

To examine whether gene transcript profiling of RNA sampled from patch tested patient skin by tape stripping (TS) could differentiate ACD from ICD and the baseline skin state (control) METHODS: Nine patients (seven females, two males; mean age 38.6 years, range 24-72 years) with confirmed ACD through patch testing were recruited. Total RNA was isolated from TS samples and relative transcript abundance was determined by quantitative real-time polymeraise chain reaction using 39 gene-specific primers.

RESULTS

TS captured gene transcripts derived from diverse skin cell types, including not only keratinocytes, but also epidermal and dermal antigen-presenting cells. Among the genes analysed in transcript profiling, genes encoding epidermal barrier components and inflammatory mediators exhibited changes in transcript abundance in ACD skin compared to ICD or control skin.

CONCLUSIONS

Our findings reveal the potential of skin TS for non-invasive biopsy during patch testing and molecular marker-based ACD diagnosis.

摘要

背景

变应性接触性皮炎(ACD)和刺激性接触性皮炎(ICD)是常见的皮肤疾病,具有重叠的临床和组织学表现,但潜在机制不同。斑贴试验是 ACD 诊断的金标准,但由于宏观反应较弱且变化,其结果的解释可能会受到干扰。

目的

通过胶带撕脱(TS)从斑贴试验患者皮肤中采集的 RNA 进行基因转录谱分析,以区分 ACD 与 ICD 和基线皮肤状态(对照)。

方法

招募了 9 名通过斑贴试验确诊为 ACD 的患者(7 名女性,2 名男性;平均年龄 38.6 岁,范围 24-72 岁)。从 TS 样本中分离总 RNA,并通过定量实时聚合酶链反应(qRT-PCR)使用 39 个基因特异性引物确定相对转录丰度。

结果

TS 捕获了源自多种皮肤细胞类型的基因转录本,不仅包括角质形成细胞,还包括表皮和真皮抗原呈递细胞。在转录谱分析中分析的基因中,编码表皮屏障成分和炎症介质的基因在 ACD 皮肤中的转录丰度与 ICD 或对照皮肤相比发生了变化。

结论

我们的发现揭示了在斑贴试验期间通过皮肤 TS 进行非侵入性活检和基于分子标志物的 ACD 诊断的潜力。

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