Department of Biosciences, Durham University, South Road, Durham DH1 3LE, UK.
The Wellcome-Wolfson Institute for Experimental Medicine, Queens University Belfast, Belfast BT9 7BL, UK.
Cells. 2024 Jul 17;13(14):1205. doi: 10.3390/cells13141205.
Systemic sclerosis (SSc) is an autoimmune connective tissue disease with a triad of features that include vascular abnormalities, inflammation and skin and lung fibrosis. At the core of the disease is the activation of myofibroblasts from quiescent fibroblasts and this can be modified by various cytokines. IL-41 is a recently described cytokine that was initially characterised as an adipokine as it was highly expressed in adipocytes and adipose tissue. However, it has recently been identified as being widely expressed and has immunomodulatory functions. This study examined the circulating levels of IL-41 and its expression in skin biopsies. We demonstrated significantly reduced levels of IL-41 in diffuse SSc that was also mirrored in the skin of SSc patients. AMPK has been proposed as a downstream target of IL-41, so we also measure mammalian target of rapamycin in skin and found that this is elevated in SSc patients. We speculate that IL-41 maybe an antifibrotic cytokine and its reduction may facilitate the activation of fibroblasts.
系统性硬化症(SSc)是一种自身免疫性结缔组织疾病,其三联征特征包括血管异常、炎症以及皮肤和肺纤维化。疾病的核心是静止成纤维细胞向肌成纤维细胞的激活,这可以被各种细胞因子所改变。IL-41 是一种最近描述的细胞因子,最初被描述为一种脂肪细胞因子,因为它在脂肪细胞和脂肪组织中高度表达。然而,最近它被确定为广泛表达,并具有免疫调节功能。本研究检测了循环中 IL-41 的水平及其在皮肤活检中的表达。我们发现在弥漫性 SSc 中 IL-41 的水平显著降低,这在 SSc 患者的皮肤中也得到了反映。AMPK 已被提议为 IL-41 的下游靶标,因此我们还在皮肤中测量了雷帕霉素的哺乳动物靶标(mTOR),发现 SSc 患者的 mTOR 升高。我们推测 IL-41 可能是一种抗纤维化细胞因子,其减少可能促进成纤维细胞的激活。