a Hospital das Clínicas de Pernambuco , Universidade Federal de Pernambuco , Recife , Brazil.
b Laboratório de Imunomodulação e Novas Abordagens Terapêuticas Suely Galdino , Universidade Federal de Pernambuco , Recife , Brazil.
Autoimmunity. 2018 Feb;51(1):1-9. doi: 10.1080/08916934.2017.1416467. Epub 2017 Dec 19.
Systemic sclerosis (SSc) is a multisystemic, complex, and rare disease of connective tissue, with high morbidity and mortality, and without specific treatment. The disease is characterized by three main principles: vascular disease, autoantibody production and inflammation, and fibrosis. Since it is well defined that SSc is characterized by elevated production of TGF-β, IL-6, and IL-1, all of them cytokines related to Th17 differentiation, the hypothesis is that this disease may be strongly related to a polarization of the immune response towards the Th17 pathway. Considering the importance of a better understanding of the pathophysiology of Th17 pathway in SSc, this article aims to propose an update for a better understanding of current knowledge on main cytokines secreted by the Th17 cells (IL-17 A, IL-21, and IL-22) and the future prospects in the current disease.
系统性硬化症(SSc)是一种多系统、复杂且罕见的结缔组织疾病,发病率和死亡率均较高,且尚无特异性治疗方法。该病的特征主要有三条:血管疾病、自身抗体产生和炎症以及纤维化。由于人们已经清楚地认识到 SSc 的特征是 TGF-β、IL-6 和 IL-1 的产生增加,所有这些细胞因子都与 Th17 分化有关,因此可以假设该疾病可能与免疫应答向 Th17 途径的强烈极化密切相关。鉴于更好地了解 SSc 中 Th17 途径的病理生理学的重要性,本文旨在提出更新内容,以更好地了解 Th17 细胞分泌的主要细胞因子(IL-17A、IL-21 和 IL-22)的当前知识,并展望该疾病的未来前景。