Department of Microbiology, Immunology and Molecular Genetics, University of Texas Health San Antonio, 7703 Floyd Curl Dr., MC7758, San Antonio, TX, 78229-3900, USA.
Department of Microbiology, Immunology and Molecular Genetics, University of Texas Health San Antonio, 7703 Floyd Curl Dr., MC7758, San Antonio, TX, 78229-3900, USA.
Curr Opin Immunol. 2022 Oct;78:102245. doi: 10.1016/j.coi.2022.102245. Epub 2022 Sep 16.
Systemic lupus erythematosus (SLE) is an autoimmune disease in which the overactivation of the immune system has been associated with metabolic alterations. Targeting the altered immunometabolism has been proposed to treat SLE patients based on their results obtained and mouse models of the disease. Here, we review the recent literature to discuss the possible origins of the alterations in the metabolism of immune cells in lupus, the dominant role of mitochondrial defects, technological advances that may move the field forward, as well as how targeting lupus immunometabolism may have therapeutic potential.
系统性红斑狼疮(SLE)是一种自身免疫性疾病,其中免疫系统的过度激活与代谢改变有关。基于研究结果和疾病的小鼠模型,提出针对改变的免疫代谢来治疗 SLE 患者。在这里,我们回顾了最近的文献,讨论了狼疮患者免疫细胞代谢改变的可能起源、线粒体缺陷的主导作用、可能推动该领域前进的技术进步,以及针对狼疮免疫代谢的治疗潜力。