Park Brandon, Kim Joshua, Baylink David J, Hino Christopher, Kwon Cedric, Tran Victoria, Xiao Jeffrey, Cao Huynh, Lee Scott, Tan Laren, Chang Andrew, Saca Luis, Matus Michael, Lobo Moreno Pamela, Schill-Depew Amy, Abdel-Azim Hisham, Mirshahidi Hamid, Xu Yi
Division of Discovery, Innovation and Regenerative Medicine, Department of Medicine, School of Medicine, Loma Linda University, Loma Linda, CA92354, USA.
Division of Hematology and Oncology, Department of Medicine, School of Medicine, Loma Linda University, Loma Linda, CA92354, USA.
J Transl Med. 2025 Jun 6;23(1):633. doi: 10.1186/s12967-025-06606-z.
Cancer immunotherapy is transforming the treatment landscape of both hematological and solid cancers. Although T-cell-based adoptive cell transfer (ACT) therapies have demonstrated initial success, several recurrent obstacles limit their long-term anti-tumor efficacy, including: (1) lack of antigen specificity; (2) poor long-term survival of transplanted T cells in vivo; and (3) a hostile tumor microenvironment (TME). While numerous approaches have been explored to enhance the antigen specificity of Chimeric Antigen Receptor (CAR) T-cell therapies, the field still lacks an effective strategy to optimize the long-term retention and in vivo expansion of engrafted T cells within the TME-a critical factor for the durable efficacy of T-cell-based immunotherapies for both blood and solid cancers. Here, we hypothesize that the success of CAR T-cell therapy can be enhanced by targeting donor T cells' ability to compete with cancer cells for key nutrients, thereby overcoming T-cell exhaustion and sustaining durable anti-tumor function in the TME. To explore this hypothesis, we first provide a comprehensively review of the current understanding of the metabolic interactions (e.g., glucose metabolism) between T cells and tumor cells. To address the challenges, we propose an innovative strategy: utilizing nutrient gene therapy (genetic overexpression of glucose transporter 1, GLUT1) to fortify the metabolic competency of adoptive CAR T-cells, deprive tumors of critical metabolites and ATP, and disrupt the TME. Altogether, our proposed approach combining precision medicine (adoptive CAR T-cell therapy) with tumor metabolism-targeting strategies offers a promising and cost-effective solution to enhance the efficacy and durability of ACT therapies, ultimately improving outcomes for cancer patients.
癌症免疫疗法正在改变血液系统癌症和实体癌的治疗格局。尽管基于T细胞的过继性细胞转移(ACT)疗法已初显成效,但一些反复出现的障碍限制了它们的长期抗肿瘤疗效,这些障碍包括:(1)缺乏抗原特异性;(2)移植的T细胞在体内长期存活率低;以及(3)恶劣的肿瘤微环境(TME)。虽然已经探索了多种方法来提高嵌合抗原受体(CAR)T细胞疗法的抗原特异性,但该领域仍然缺乏一种有效的策略来优化植入的T细胞在TME中的长期留存和体内扩增,而这是基于T细胞的免疫疗法对血液和实体癌产生持久疗效的关键因素。在此,我们假设,通过靶向供体T细胞与癌细胞竞争关键营养物质的能力,可以提高CAR T细胞疗法的成功率,从而克服T细胞耗竭并在TME中维持持久的抗肿瘤功能。为了探索这一假设,我们首先全面综述了目前对T细胞与肿瘤细胞之间代谢相互作用(例如葡萄糖代谢)的理解。为应对这些挑战,我们提出了一种创新策略:利用营养基因疗法(葡萄糖转运蛋白1,GLUT1的基因过表达)来增强过继性CAR T细胞的代谢能力,剥夺肿瘤关键代谢物和ATP,并破坏TME。总之,我们提出的将精准医学(过继性CAR T细胞疗法)与肿瘤代谢靶向策略相结合的方法,为提高ACT疗法的疗效和持久性提供了一种有前景且经济高效的解决方案,最终改善癌症患者的治疗效果。