School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261053, China.
School of Basic Medical Sciences, Shandong Second Medical University, Weifang 261053, China.
Cytokine. 2024 Jul;179:156623. doi: 10.1016/j.cyto.2024.156623. Epub 2024 Apr 28.
Systemic lupus erythematosus (SLE) is a connective tissue disorder that affects various body systems. Both the innate and adaptive immunity contribute to the onset and progression of SLE. The main mechanism of SLE is an excessive immune response of immune cells to autoantigens, which leads to systemic inflammation and inflammation-induced organ damage. Notably, a subset of innate immune cells known as innate lymphoid cells (ILCs) has recently emerged. ILCs are pivotal in the early stages of infection; participate in immune responses, inflammation, and tissue repair; and regulate the immune function of the body by resisting pathogens and regulating autoimmune inflammation and metabolic homeostasis. Thus, ILCs dysfunction can lead to autoimmune diseases. This review discusses the maturation of ILCs, the potential mechanisms by which ILCs exacerbate SLE pathogenesis, and their contributions to organ inflammatory deterioration in SLE.
系统性红斑狼疮(SLE)是一种影响多种身体系统的结缔组织疾病。先天免疫和适应性免疫都有助于 SLE 的发病和进展。SLE 的主要机制是免疫细胞对自身抗原的过度免疫反应,导致全身炎症和炎症引起的器官损伤。值得注意的是,最近出现了一类称为固有淋巴细胞(ILC)的先天免疫细胞。ILC 在感染的早期阶段至关重要;参与免疫反应、炎症和组织修复;通过抵抗病原体和调节自身免疫炎症及代谢稳态来调节身体的免疫功能。因此,ILC 功能障碍可导致自身免疫性疾病。这篇综述讨论了 ILC 的成熟、ILC 加剧 SLE 发病机制的潜在机制,以及它们在 SLE 中对器官炎症恶化的贡献。