Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Inflamm Res. 2023 Jul;72(7):1513-1524. doi: 10.1007/s00011-023-01763-7. Epub 2023 Jul 6.
Oral lichen planus (OLP) is a T cell-mediated chronic autoimmune disease, whose pathogenesis and etiology are not entirely understood. OLP is characterized by subepithelial lymphocyte infiltration and elevated intra-epithelial lymphocytes. The majority of lamina propria lymphocytes are CD4 T cells. CD4 helper T (Th) cells play a crucial role in activating CD8 cytotoxic T cells (CTLs) through interactions and cytokine production. Th1 and Th2 cells are well-accepted to be associated with OLP pathogenesis. However, OLP treatment is challenging yet, the more information we have about the pathology of OLP, the easier it will be treated. With the discovery of Th17 cells in recent years and the demonstration of their role in autoimmune disease, many researchers started to investigate the role of Th17 in the pathogenesis of OLP.
To make up this review, studies covering the role of TH17 in different types of lichen planus were selected from major databases.
As we review in this article, Th17 cells and their signature cytokines play an important role in OLP pathogenesis. As well, utilizing some anti-IL-17 antibodies showed promising results in improving the disease; however, more studies are still needed to better understand and treat OLP.
口腔扁平苔藓(OLP)是一种 T 细胞介导的慢性自身免疫性疾病,其发病机制和病因尚不完全清楚。OLP 的特征是上皮下淋巴细胞浸润和上皮内淋巴细胞升高。大多数固有层淋巴细胞是 CD4 T 细胞。CD4 辅助 T(Th)细胞通过相互作用和细胞因子产生在激活 CD8 细胞毒性 T 细胞(CTL)中起关键作用。Th1 和 Th2 细胞被认为与 OLP 的发病机制有关。然而,OLP 的治疗具有挑战性,我们对 OLP 病理学的了解越多,治疗就越容易。随着近年来 Th17 细胞的发现及其在自身免疫性疾病中的作用的证明,许多研究人员开始研究 Th17 在 OLP 发病机制中的作用。
为了撰写这篇综述,我们从主要数据库中选择了涵盖 Th17 在不同类型扁平苔藓中作用的研究。
正如我们在本文中综述的那样,Th17 细胞及其特征性细胞因子在 OLP 的发病机制中起重要作用。此外,使用一些抗 IL-17 抗体显示出改善疾病的有希望的结果;然而,仍需要更多的研究来更好地理解和治疗 OLP。