Department of Rheumatology and Immunology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Department of Clinical Medicine "5 + 3" Integration, The First Clinical College, Anhui Medical University, Hefei, China.
Front Immunol. 2022 May 18;13:894847. doi: 10.3389/fimmu.2022.894847. eCollection 2022.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by multiple organ dysfunction resulting from the production of multiple autoantibodies and adaptive immune system abnormalities involving T and B lymphocytes. In recent years, inflammasomes have been recognized as an important component of innate immunity and have attracted increasing attention because of their pathogenic role in SLE. In short, inflammasomes regulate the abnormal differentiation of immune cells, modulate pathogenic autoantibodies, and participate in organ damage. However, due to the clinical heterogeneity of SLE, the pathogenic roles of inflammasomes are variable, and thus, the efficacy of inflammasome-targeting therapies is uncertain. To provide a foundation for the development of such therapeutic strategies, in this paper, we review the role of different inflammasomes in the pathogenesis of SLE and their correlation with clinical phenotypes and propose some corresponding treatment strategies.
系统性红斑狼疮(SLE)是一种自身免疫性疾病,其特征是多种器官功能障碍,这是由多种自身抗体的产生和涉及 T 和 B 淋巴细胞的适应性免疫系统异常引起的。近年来,炎症小体已被认为是先天免疫的重要组成部分,由于其在 SLE 中的致病作用而引起了越来越多的关注。简而言之,炎症小体调节免疫细胞的异常分化,调节致病性自身抗体,并参与器官损伤。然而,由于 SLE 的临床异质性,炎症小体的致病作用是可变的,因此,炎症小体靶向治疗的疗效是不确定的。为了为这种治疗策略的发展提供基础,在本文中,我们综述了不同炎症小体在 SLE 发病机制中的作用及其与临床表型的相关性,并提出了一些相应的治疗策略。