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:Nanoparticle-mediated universal CAR-T therapy.
Nanoparticle-mediated universal CAR-T therapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
近年来,嵌合抗原受体(CAR)T 细胞治疗在血液系统恶性肿瘤中取得了显著成功,推动了肿瘤免疫治疗领域的重要进展。然而,传统 CAR-T 治疗需要富集患者自身白细胞,在体外制备 CAR-T 细胞。这种个体化模式制造流程复杂且耗时,导致成本高、可及性较差。现成的通用型 CAR-T 策略有望降低生产成本并实现及时给药,因此可作为传统 CAR-T 治疗的理想替代方案。利用纳米载体进行靶向基因递送,是实现通用型 CAR-T 治疗的途径之一:具有生物相容性且用途广泛的纳米颗粒可将 CAR 基因递送至体内生成 CAR-T 细胞。纳米颗粒介导的 CAR-T 细胞原位生成具有多项优势,包括降低成本、简化生产流程和缩短给药等待时间。该策略有望成为当前自体 CAR-T 细胞生产模式的一种潜在低成本替代方案,从而推动 CAR-T 治疗的普及与改进。
In recent years, chimeric antigen receptor (CAR)-T cell therapy has been highly successful in treating hematological malignancies, leading to significant advancements in the cancer immunotherapy field.
However, the typical CAR-T therapy necessitates the enrichment of patients' own leukocytes for ex vivo production of CAR-T cells, this customized pattern requires a complicated and time-consuming manufacturing procedure, making it costly and less accessible. The off-the-shelf universal CAR-T strategy could reduce manufacturing costs and realize timely drug administration, presenting as an ideal substitute for typical CAR-T therapy.
Utilizing nanocarriers for targeted gene delivery is one of the approaches for the realization of universal CAR-T therapy, as biocompatible and versatile nanoparticles could deliver CAR genes to generate CAR-T cells in vivo.
Nanoparticle-mediated in situ generation of CAR-T cells possesses multiple advantages, including lowered cost, simplified manufacturing procedure, and shortened administration time, this strategy is anticipated to provide a potentially cost-effective alternative to current autologous CAR-T cell manufacturing, thus facilitating the prevalence and improvement of CAR-T therapy.
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