Deng Jingwen, Tan Siyi, Liu Ruonan, Yu Wanlin, Chen Haiming, Tang Nan, Han Ling, Lu Chuanjian
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, China.
Front Pharmacol. 2021 Jan 18;11:563433. doi: 10.3389/fphar.2020.563433. eCollection 2020.
Psoriasis is a chronic inflammatory skin disease that is associated with multiple coexisting conditions. Extensive literature suggests that psoriasis is a T-cell-mediated condition, and its pathogenesis is related to dysfunction of the immune system. Myeloid-derived suppressor cells (MDSCs) are a group of heterogeneous myeloid cells that have suppressive effects on T cells. MDSCs are present at very low levels in healthy individuals but can substantially expand in tumours or inflammatory conditions. PSORI-CM02, a Chinese medical formula designed based on the Chinese medicine theory (), has been prescribed extensively for psoriasis therapy and shows a stable clinical effect and safety. This study discusses the mechanisms of MDSCs involved in disease development and therapeutic progress. Our data provides evidence that monocytic myeloid-derived suppressor cells (M-MDSCs) play a role in IMQ-induced psoriatic dermatitis. Functional characterization and correlation analysis indicated that MDSCs are positively correlated with Th17 cells. PSORI-CM02 alleviated IMQ-induced psoriatic dermatitis and suppressed the proliferation of Th17 cells via M-MDSC-induced Arg1 upregulation, suggesting M-MDSCs could be a novel therapeutic target for psoriasis, and PSORI-CM02 exerted its effects via the perturbation of M-MDSCs and Th17 cell crosstalk.
银屑病是一种慢性炎症性皮肤病,与多种并存疾病相关。大量文献表明,银屑病是一种T细胞介导的疾病,其发病机制与免疫系统功能障碍有关。髓系来源的抑制细胞(MDSCs)是一组对T细胞具有抑制作用的异质性髓系细胞。MDSCs在健康个体中水平极低,但在肿瘤或炎症状态下可大量扩增。PSORI-CM02是一种基于中医理论设计的中药方剂,已被广泛用于银屑病治疗,且显示出稳定的临床疗效和安全性。本研究探讨了MDSCs在疾病发展和治疗进展中的作用机制。我们的数据提供了证据,表明单核细胞源性髓系抑制细胞(M-MDSCs)在咪喹莫特诱导的银屑病性皮炎中发挥作用。功能表征和相关性分析表明,MDSCs与Th17细胞呈正相关。PSORI-CM02减轻了咪喹莫特诱导的银屑病性皮炎,并通过M-MDSC诱导的精氨酸酶1(Arg1)上调抑制了Th17细胞的增殖,提示M-MDSCs可能是银屑病的一个新治疗靶点,且PSORI-CM02通过干扰M-MDSCs和Th17细胞的相互作用发挥其作用。