Division of Allergy, Asthma, and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
Int J Mol Sci. 2021 Jul 26;22(15):7960. doi: 10.3390/ijms22157960.
Monocytes (Mos) and macrophages (Mφs) are key players in the innate immune system and are critical in coordinating the initiation, expansion, and regression of many autoimmune diseases. In addition, they display immunoregulatory effects that impact inflammation and are essential in tissue repair and regeneration. Juvenile idiopathic arthritis (JIA) is an umbrella term describing inflammatory joint diseases in children. Accumulated evidence suggests a link between Mo and Mφ activation and JIA pathogenesis. Accordingly, topics regarding the signals and mechanisms regulating Mo and Mφ activation leading to pathologies in patients with JIA are of great interest. In this review, we critically summarize recent advances in the understanding of how Mo and Mφ activation is involved in JIA pathogenesis and focus on the signaling pathways and mechanisms participating in the related cell activation processes.
单核细胞 (Mos) 和巨噬细胞 (Mφs) 是先天免疫系统的关键参与者,在协调许多自身免疫性疾病的发生、发展和消退中至关重要。此外,它们还具有免疫调节作用,影响炎症,对组织修复和再生至关重要。幼年特发性关节炎 (JIA) 是一个总称,用于描述儿童的炎症性关节疾病。越来越多的证据表明,Mo 和 Mφ 的激活与 JIA 的发病机制之间存在联系。因此,关于调节 Mo 和 Mφ 激活导致 JIA 患者发生病理的信号和机制的相关主题非常重要。在这篇综述中,我们批判性地总结了目前对 Mo 和 Mφ 激活如何参与 JIA 发病机制的理解的最新进展,并重点关注参与相关细胞激活过程的信号通路和机制。