Department of Neurological Surgery, University of California San Francisco, San Francisco, CA 94143, USA.
Helen Diller Family Comprehensive Cancer Center, San Francisco, CA 94158, USA.
Cells. 2024 Apr 23;13(9):726. doi: 10.3390/cells13090726.
Glioblastoma (GBM) is the most common primary malignant brain tumor, with a median overall survival of less than 2 years and a nearly 100% mortality rate under standard therapy that consists of surgery followed by combined radiochemotherapy. Therefore, new therapeutic strategies are urgently needed. The success of chimeric antigen receptor (CAR) T cells in hematological cancers has prompted preclinical and clinical investigations into CAR-T-cell treatment for GBM. However, recent trials have not demonstrated any major success. Here, we delineate existing challenges impeding the effectiveness of CAR-T-cell therapy for GBM, encompassing the cold (immunosuppressive) microenvironment, tumor heterogeneity, T-cell exhaustion, local and systemic immunosuppression, and the immune privilege inherent to the central nervous system (CNS) parenchyma. Additionally, we deliberate on the progress made in developing next-generation CAR-T cells and novel innovative approaches, such as low-intensity pulsed focused ultrasound, aimed at surmounting current roadblocks in GBM CAR-T-cell therapy.
胶质母细胞瘤(GBM)是最常见的原发性恶性脑肿瘤,中位总生存期不到 2 年,在标准治疗(包括手术联合放化疗)下,几乎 100%的死亡率。因此,迫切需要新的治疗策略。嵌合抗原受体(CAR)T 细胞在血液系统癌症中的成功促使人们对 CAR-T 细胞治疗 GBM 进行了临床前和临床研究。然而,最近的试验并没有显示出任何重大成功。在这里,我们描述了阻碍 CAR-T 细胞治疗 GBM 有效性的现有挑战,包括冷(免疫抑制)微环境、肿瘤异质性、T 细胞衰竭、局部和全身免疫抑制以及中枢神经系统(CNS)实质固有的免疫特权。此外,我们还讨论了在开发下一代 CAR-T 细胞和新型创新方法方面取得的进展,例如低强度脉冲聚焦超声,旨在克服 GBM CAR-T 细胞治疗中的当前障碍。