Givian Aliakbar, Azizan Amin, Jamshidi Ahmadreza, Mahmoudi Mahdi, Farhadi Elham
Rheumatology Research Center, Tehran University of Medical Science, Tehran, Iran.
Department of Immunology, School of Medicine, Semnan University of Medical Science, Semnan, Iran.
J Transl Autoimmun. 2025 Jan 4;10:100267. doi: 10.1016/j.jtauto.2025.100267. eCollection 2025 Jun.
Iron is a crucial element for living organism in terms of oxygen transport, hematopoiesis, enzymatic activity, mitochondrial respiratory chain function and also immune system function. The human being has evolved a mechanism to regulate body iron. In some rheumatic diseases such as rheumatoid arthritis (RA), systemic lupus erythematous (SLE), systemic sclerosis (SSc), ankylosing spondylitis (AS), and gout, this balanced iron regulation is impaired. Altered iron homeostasis can contribute to disease progression through ROS production, fibrosis, inflammation, abnormal bone homeostasis, NETosis and cell senescence. In this review, we have focused on the iron metabolism in rheumatic disease and its role in disease progression.
就氧气运输、造血、酶活性、线粒体呼吸链功能以及免疫系统功能而言,铁是生物体的关键元素。人类已经进化出一种调节体内铁的机制。在某些风湿性疾病中,如类风湿关节炎(RA)、系统性红斑狼疮(SLE)、系统性硬化症(SSc)、强直性脊柱炎(AS)和痛风,这种平衡的铁调节会受到损害。铁稳态的改变可通过活性氧生成、纤维化、炎症、异常骨稳态、中性粒细胞胞外陷阱形成和细胞衰老促进疾病进展。在这篇综述中,我们重点关注了风湿性疾病中的铁代谢及其在疾病进展中的作用。