Dasgupta Debolina, Tripathi Aprajita, Griffard-Smith Rachel, Yellapu Nandakumar, Dhorajiya Poojaben, Pyaram Kalyani
Department of Cancer Biology, University of Kansas, Medical Center, Kansas City, KS, United States.
Department of Biostatistics and Data Sciences, University of Kansas, Medical Center, Kansas City, KS, United States.
J Immunol. 2025 Aug 1;214(8):1951-1968. doi: 10.1093/jimmun/vkaf117.
RTA-408, also known as Omaveloxolone, is an FDA-approved drug for treating Friedrich's Ataxia, a neurological disorder. It is a triterpenoid compound that activates nuclear factor erythroid 2-related factor 2 (NRF2), a key regulator of cellular redox balance. In this study, we explored the impact of RTA-408 on T cells and evaluated its therapeutic potential in inflammatory bowel disease (IBD). In vitro activation of murine and human T cells in the presence of RTA-408 resulted in suppressed proliferation, reduced expression of IFN-γ, cytotoxic granules and IL-17, but enhanced frequency of Foxp3+ Treg cells. Treatment of Nrf2-deficient T cells with RTA-408 revealed that while the reduction in CD69 expression, IL-2, and IFN-γ levels is NRF2-dependent, the suppression of T cell proliferation and granzyme B/perforin expression occurs independently of NRF2. In vivo administration of RTA-408 alleviated the disease severity in DSS-induced colitis mice by decreasing colonic T cell counts and their inflammatory cytokine production. Additionally, ex vivo treatment of T cells from IBD patients with RTA-408 reduced their expansion and IL-17 expression. Transcriptomic and metabolic analyses revealed that RTA-408 reduces glycolysis and mitochondrial respiration in T cells and reprograms their metabolism towards pentose phosphate pathway and glutaminolysis. Our findings highlight the potential of RTA-408 as a modulator of T cell homeostasis, metabolism, and inflammation, supporting its repurposing for inflammatory diseases like IBD.
RTA-408,也被称为奥马韦洛酮,是一种经美国食品药品监督管理局(FDA)批准用于治疗弗里德赖希共济失调(一种神经疾病)的药物。它是一种三萜类化合物,可激活细胞氧化还原平衡的关键调节因子核因子红细胞2相关因子2(NRF2)。在本研究中,我们探讨了RTA-408对T细胞的影响,并评估了其在炎症性肠病(IBD)中的治疗潜力。在RTA-408存在的情况下对小鼠和人类T细胞进行体外激活,导致细胞增殖受到抑制,IFN-γ、细胞毒性颗粒和IL-17的表达降低,但Foxp3+调节性T细胞的频率增加。用RTA-408处理Nrf2缺陷型T细胞发现,虽然CD69表达、IL-2和IFN-γ水平的降低依赖于NRF2,但T细胞增殖的抑制以及颗粒酶B/穿孔素的表达独立于NRF2发生。在体内给予RTA-408可通过减少结肠T细胞数量及其炎性细胞因子的产生来减轻葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠的疾病严重程度。此外,用RTA-408对IBD患者的T细胞进行离体处理可减少其扩增和IL-17的表达。转录组学和代谢分析表明,RTA-408可降低T细胞中的糖酵解和线粒体呼吸作用,并将其代谢重编程为磷酸戊糖途径和谷氨酰胺分解代谢。我们的研究结果突出了RTA-408作为T细胞稳态、代谢和炎症调节剂的潜力,支持将其重新用于治疗IBD等炎症性疾病。