Department of Pathology, Microbiology, and Immunology, Vanderbilt Center for Immunobiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Department of Pathology, Microbiology, and Immunology, Vanderbilt Center for Immunobiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Mol Cell. 2020 Jun 18;78(6):1019-1033. doi: 10.1016/j.molcel.2020.05.034.
The growing field of immune metabolism has revealed promising indications for metabolic targets to modulate anti-cancer immunity. Combination therapies involving metabolic inhibitors with immune checkpoint blockade (ICB), chemotherapy, radiation, and/or diet now offer new approaches for cancer therapy. However, it remains uncertain how to best utilize these strategies in the context of the complex tumor microenvironment (TME). Oncogene-driven changes in tumor cell metabolism can impact the TME to limit immune responses and present barriers to cancer therapy. These changes also reveal opportunities to reshape the TME by targeting metabolic pathways to favor immunity. Here we explore current strategies that shift immune cell metabolism to pro-inflammatory states in the TME and highlight a need to better replicate physiologic conditions to select targets, clarify mechanisms, and optimize metabolic inhibitors. Unifying our understanding of these pathways and interactions within the heterogenous TME will be instrumental to advance this promising field and enhance immunotherapy.
免疫代谢领域的发展揭示了代谢靶点在调节抗肿瘤免疫方面的广阔前景。代谢抑制剂与免疫检查点抑制剂(ICB)、化疗、放疗和/或饮食相结合的联合疗法为癌症治疗提供了新的方法。然而,在复杂的肿瘤微环境(TME)背景下,如何最好地利用这些策略仍然不确定。肿瘤细胞代谢的致癌驱动变化会影响 TME,限制免疫反应,并对癌症治疗构成障碍。这些变化也为通过靶向代谢途径来促进免疫提供了重塑 TME 的机会。在这里,我们探讨了当前在 TME 中改变免疫细胞代谢以促进炎症状态的策略,并强调需要更好地复制生理条件来选择靶点、阐明机制和优化代谢抑制剂。统一我们对异质性 TME 中这些途径和相互作用的理解,对于推进这一有前途的领域和增强免疫疗法至关重要。