AbbVie Inc, North Chicago, Illinois, USA.
Department of Dermatology, Northwestern University, Chicago, Illinois, USA.
Exp Dermatol. 2022 Jul;31(7):1036-1047. doi: 10.1111/exd.14551. Epub 2022 Mar 7.
Psoriasis vulgaris is an inflammatory skin disease that affects 2%-3% of the population worldwide. One of the major challenges in discovering novel therapies is the poor translatability of animal models to human disease. Therefore, it is imperative to develop human preclinical models of psoriasis that are amenable to pharmacological intervention. Here, we report a 3-D reconstituted human epidermis (RHE) culture system treated with cytokines commonly associated with psoriasis (TNFα, IL-17A and IL-22) that reproduced some key features of the human disease. The effects on epidermal morphology, gene transcription and cytokine production, which are dysregulated in psoriasis were assessed. Certain morphological features of psoriatic epidermis were evident in cytokine-stimulated RHEs, including hypogranulosis and parakeratosis. In addition, RHEs responded to a cytokine mix in a dose-dependent manner by expressing genes and proteins associated with impaired keratinocyte differentiation (keratin 10/K10, loricrin), innate immune responses (S100A7, DEFB4, elafin) and inflammation (IL-1α, IL-6, IL-8, IL-10, IL-12/23p40, IL-36γ, GM-CSF and IFNγ) typical of psoriasis. These disease-relevant changes in morphology, gene transcription and cytokine production were robustly attenuated by pharmacologically blocking TNFα/IL-17A-induced NF-κB activation with IKK-2 inhibitor IV. Conversely, inhibition of IL-22-induced JAK1 signalling with ABT-317 strongly attenuated morphological features of the disease but had no effect on NFκB-dependent cytokine production, suggesting distinct mechanisms of action by the cytokines driving psoriasis. These data support the use of cytokine-induced RHE models for identifying and targeting keratinocyte signalling pathways important for disease progression and may provide translational insights into novel keratinocyte mechanisms for novel psoriasis therapies.
寻常型银屑病是一种炎症性皮肤病,影响全球 2%-3%的人口。在发现新疗法的过程中,一个主要挑战是动物模型向人类疾病的转化效果不佳。因此,开发可进行药物干预的人类银屑病临床前模型至关重要。在此,我们报告了一种经细胞因子处理的 3D 重建人表皮(RHE)培养系统,该系统中使用的细胞因子通常与银屑病相关(TNFα、IL-17A 和 IL-22),可再现人类疾病的一些关键特征。我们评估了表皮形态、基因转录和细胞因子产生的变化,这些变化在银屑病中失调。在细胞因子刺激的 RHE 中,银屑病表皮的某些形态特征明显,包括颗粒减少和角化不全。此外,RHE 以剂量依赖性方式对细胞因子混合物作出反应,表达与角蛋白细胞分化受损(角蛋白 10/K10、兜甲蛋白)、先天免疫反应(S100A7、DEFB4、elafin)和炎症(IL-1α、IL-6、IL-8、IL-10、IL-12/23p40、IL-36γ、GM-CSF 和 IFNγ)相关的基因和蛋白,这些都是银屑病的典型特征。用 IKK-2 抑制剂 IV 抑制 TNFα/IL-17A 诱导的 NF-κB 激活,可显著减弱这些与疾病相关的形态、基因转录和细胞因子产生的变化。相反,用 ABT-317 抑制 IL-22 诱导的 JAK1 信号传导强烈减弱了疾病的形态特征,但对 NFκB 依赖性细胞因子产生没有影响,这表明细胞因子驱动银屑病的作用机制不同。这些数据支持使用细胞因子诱导的 RHE 模型来识别和靶向对角蛋白细胞信号通路重要的疾病进展,并为新型银屑病疗法的新型角蛋白细胞机制提供转化见解。