Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
Br J Dermatol. 2015 Aug;173(2):436-47. doi: 10.1111/bjd.13721. Epub 2015 Jul 14.
Tumour necrosis factor (TNF)-α inhibition is an effective treatment for moderate to severe plaque-type psoriasis. A change in the cytokine expression profile occurs in the skin after 4 days of treatment, preceding any clinical or histological improvements. MicroRNAs (miRNAs) are important post-transcriptional regulators of gene expression, but miRNA expression has never been studied in psoriatic skin during treatment.
To investigate changes in miRNA expression in psoriatic skin during adalimumab treatment and to compare results with changes in miRNA expression in a mouse model of Aldara-induced psoriasis-like skin inflammation.
Punch biopsies were obtained from nonlesional and lesional psoriatic skin during adalimumab treatment. In the mouse model of Aldara-induced skin inflammation, biopsies were obtained from TNF-α knockout (KO), IL-17A KO and wild-type mice. miRNA expression levels were analysed with microarray, reverse transcriptase quantitative polymerase chain reaction and in situ hybridization.
In psoriatic skin, no changes in miRNA expression were seen 4 days after treatment initiation. After 14 days of treatment, the expression of several miRNAs was normalized towards the level seen in nonlesional skin before treatment. miR-23b expression increased after 14 days of treatment and remained high for 84 days, despite unaltered levels at baseline. In the mouse model of Aldara-induced skin inflammation, the level of miR-146a increased, whereas no regulation was seen for miR-203, miR-214-3p, miR-125a, miR-23b or let-7d-5p.
This study demonstrates that the changes seen in the cytokine expression levels after 4 days of treatment with adalimumab are not facilitated by early changes in miRNA expression.
肿瘤坏死因子 (TNF)-α 抑制剂是治疗中重度斑块状银屑病的有效方法。在治疗 4 天后,皮肤中的细胞因子表达谱发生变化,早于任何临床或组织学改善。microRNAs(miRNAs)是基因表达的重要转录后调控因子,但在 TNF-α 抑制剂治疗银屑病皮肤时,从未研究过 miRNA 的表达。
研究 TNF-α 抑制剂治疗过程中银屑病皮肤中 miRNA 表达的变化,并将结果与 Aldara 诱导的银屑病样皮肤炎症小鼠模型中 miRNA 表达的变化进行比较。
在 TNF-α 抑制剂治疗过程中,从非皮损和皮损银屑病皮肤中获取活检。在 Aldara 诱导的皮肤炎症小鼠模型中,从 TNF-α 敲除(KO)、IL-17A KO 和野生型小鼠中获取活检。使用微阵列、逆转录定量聚合酶链反应和原位杂交分析 miRNA 表达水平。
在银屑病皮肤中,治疗开始后 4 天未观察到 miRNA 表达的变化。治疗 14 天后,几种 miRNA 的表达水平向治疗前非皮损皮肤的水平正常化。miR-23b 的表达在治疗 14 天后增加,并持续 84 天高表达,尽管基线水平不变。在 Aldara 诱导的皮肤炎症小鼠模型中,miR-146a 的水平增加,而 miR-203、miR-214-3p、miR-125a、miR-23b 或 let-7d-5p 未见调节。
本研究表明,在 TNF-α 抑制剂治疗 4 天后观察到的细胞因子表达水平的变化,不是由早期 miRNA 表达变化引起的。