Lee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore; Interdisciplinary Graduate Programme, NTU Institute for Health Technologies (HealthTech NTU), Nanyang Technological University Singapore, Singapore.
EBioMedicine. 2022 Sep;83:104216. doi: 10.1016/j.ebiom.2022.104216. Epub 2022 Aug 17.
The tumour microenvironment (TME) imposes a major obstacle to infiltrating T-lymphocytes and suppresses their function. Several immune checkpoint proteins that interfere with ligand/receptor interactions and impede T-cell anti-tumour responses have been identified. Immunotherapies that block immune checkpoints have revolutionized the treatment paradigm for many patients with advanced-stage tumours. However, metabolic constraints and soluble factors that exist within the TME exacerbate the functional exhaustion of tumour-infiltrating T-cells. Here we review these multifactorial constraints and mechanisms - elevated immunosuppressive metabolites and enzymes, nutrient insufficiency, hypoxia, increased acidity, immense amounts of extracellular ATP and adenosine, dysregulated bioenergetic and purinergic signalling, and ionic imbalance - that operate in the TME and collectively suppress T-cell function. We discuss how scientific advances could help overcome the complex TME obstacles for tumour-infiltrating T-lymphocytes, aiming to stimulate further research for developing new therapeutic strategies by harnessing the full potential of the immune system in combating cancer.
肿瘤微环境(TME)对浸润性 T 淋巴细胞构成重大障碍,并抑制其功能。已经鉴定出几种免疫检查点蛋白,这些蛋白干扰配体/受体相互作用并阻碍 T 细胞抗肿瘤反应。阻断免疫检查点的免疫疗法已经彻底改变了许多晚期肿瘤患者的治疗模式。然而,TME 中存在的代谢限制和可溶性因子加剧了肿瘤浸润 T 细胞的功能耗竭。在这里,我们回顾这些多因素限制和机制——升高的免疫抑制代谢物和酶、营养不足、缺氧、酸度增加、大量细胞外 ATP 和腺苷、代谢和嘌呤能信号失调以及离子失衡——它们在 TME 中共同作用并抑制 T 细胞功能。我们讨论了科学进步如何有助于克服肿瘤浸润性 T 淋巴细胞的复杂 TME 障碍,旨在通过充分利用免疫系统对抗癌症的潜力来刺激新的治疗策略的研究。