Repasky Elizabeth, Mohammadpour Hemn
Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA
Cell Stress Biology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA
J Immunother Cancer. 2025 May 2;13(5):e011609. doi: 10.1136/jitc-2025-011609.
A tumor's ability to attract innervation is a critical factor in tumor progression and immune escape, with the sympathetic nervous system playing a major role. Catecholamines released by sympathetic nerves activate adrenergic receptors on tumor cells, enhancing growth and resistance to therapies, while activation of adrenergic receptors on immune cells triggers immunosuppressive activity in the tumor microenvironment. Nerve growth factor (NGF) produced by tumor cells is a key driver of tumor innervation, making it a promising target for novel therapeutic strategies. In this commentary, we highlight a recent study by Yang , which examines NGF single-chain variable fragment (scFv)-secreting chimeric antigen receptor(CAR) T cells and the impact of NGF neutralization by CAR T cells on CAR T-cell function and the remodeling of the tumor microenvironment. This work shows that we may be able to exploit a tumor-derived survival factor as a vulnerability and a means to enhance antitumor immune activity.
肿瘤吸引神经支配的能力是肿瘤进展和免疫逃逸的关键因素,其中交感神经系统起主要作用。交感神经释放的儿茶酚胺激活肿瘤细胞上的肾上腺素能受体,增强肿瘤生长和对治疗的抗性,而免疫细胞上肾上腺素能受体的激活会引发肿瘤微环境中的免疫抑制活性。肿瘤细胞产生的神经生长因子(NGF)是肿瘤神经支配的关键驱动因素,使其成为新型治疗策略的一个有前景的靶点。在这篇评论中,我们重点介绍了杨等人最近的一项研究,该研究考察了分泌NGF单链可变片段(scFv)的嵌合抗原受体(CAR)T细胞,以及CAR T细胞对NGF的中和作用对CAR T细胞功能和肿瘤微环境重塑的影响。这项工作表明,我们或许能够利用一种肿瘤衍生的生存因子作为一个弱点以及增强抗肿瘤免疫活性的一种手段。