CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Advances in Nanotechnology Development to Overcome Current Roadblocks in CAR-T Therapy for Solid Tumors.
Advances in Nanotechnology Development to Overcome Current Roadblocks in CAR-T Therapy for Solid Tumors.
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CAR-T 细胞疗法治疗血液系统肿瘤已取得显著成功,美国食品药品监督管理局已批准5种CAR-T 疗法。然而,CAR-T 治疗实体瘤的疗效并不理想。目前实体瘤CAR-T 细胞面临三大障碍。第一,缺乏能够识别实体瘤部位抗原的通用CAR,加之肿瘤结构致密,使CAR-T 细胞难以定位到实体瘤内。第二,肿瘤微环境中的可溶性抑制因子和免疫抑制细胞会抑制甚至灭活T细胞。第三,CAR-T 细胞体内存活和增殖率低,显著影响治疗效果。作为一种新兴方法,纳米技术在促进细胞增殖、激活T细胞和重新启动免疫应答方面潜力巨大。本文综述纳米技术如何通过多种方法改造CAR-T 细胞,以提高实体瘤治疗效果。
Chimeric antigen receptor T cell (CAR-T) therapy for the treatment of hematologic tumors has achieved remarkable success, with five CAR-T therapies approved by the United States Food and Drug Administration.
However, the efficacy of CAR-T therapy against solid tumors is not satisfactory. There are three existing hurdles in CAR-T cells for solid tumors. First, the lack of a universal CAR to recognize antigens at the site of solid tumors and the compact tumor structure make it difficult for CAR-T cells to locate in solid tumors. Second, soluble inhibitors and suppressive immune cells in the tumor microenvironment can inhibit or even inactivate T cells.
Third, low survival and proliferation rates of CAR-T cells in vivo significantly influence the therapeutic effect. As an emerging method, nanotechnology has a great potential to enhance cell proliferation, activate T cells, and restarting the immune response. In this review, we discuss how nanotechnology can modify CAR-T cells through variable methods to improve the therapeutic effect of solid tumors.
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