Phillip West Andrew, McGuire Peter J
The Jackson Laboratory, Bar Harbor, ME 04609, USA.
National Human Genome Research Institute, Bethesda, MD 20892, USA.
Curr Opin Immunol. 2025 May 26;95:102566. doi: 10.1016/j.coi.2025.102566.
Mitochondrial diseases (MtD) provide a unique window into the complex interplay between metabolism and immune function. These rare disorders, caused by defects in oxidative phosphorylation, result in bioenergetic deficiencies that disrupt multiple organ systems. While traditionally studied for their metabolic impact, MtD also profoundly affect the immune system, altering both innate and adaptive responses. This review explores how mitochondrial dysfunction shapes immune dysregulation, influencing thymocyte maturation, regulatory T cells, and B cell function while also driving innate immune activation through mitochondrial DNA instability and type I interferon signaling. Additionally, MtD highlight an emerging overlap between inborn errors of metabolism and inborn errors of immunity, revealing shared pathways that connect mitochondrial dysfunction to immune deficiencies and inflammatory disease. Studying MtD not only advances our understanding of immunometabolism but also provides critical insights into more common inflammatory and autoimmune conditions, offering potential therapeutic targets that extend beyond rare mitochondrial disorders.
线粒体疾病(MtD)为了解新陈代谢与免疫功能之间复杂的相互作用提供了一个独特的窗口。这些由氧化磷酸化缺陷引起的罕见疾病会导致生物能量缺乏,进而扰乱多个器官系统。虽然传统上人们研究它们是因为其对新陈代谢的影响,但线粒体疾病也会深刻影响免疫系统,改变先天免疫和适应性免疫反应。本综述探讨了线粒体功能障碍如何塑造免疫失调,影响胸腺细胞成熟、调节性T细胞和B细胞功能,同时还通过线粒体DNA不稳定性和I型干扰素信号传导驱动先天免疫激活。此外,线粒体疾病凸显了先天性代谢缺陷和先天性免疫缺陷之间新出现的重叠,揭示了将线粒体功能障碍与免疫缺陷和炎症性疾病联系起来的共同途径。研究线粒体疾病不仅能增进我们对免疫代谢的理解,还能为更常见的炎症和自身免疫性疾病提供关键见解,提供超越罕见线粒体疾病的潜在治疗靶点。