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:Tumor-Associated Extracellular Matrix Obstacles for CAR-T Cell Therapy: Approaches to Overcoming.
Tumor-Associated Extracellular Matrix Obstacles for CAR-T Cell Therapy: Approaches to Overcoming.
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嵌合抗原受体(CAR)-T细胞疗法在多种血液系统恶性肿瘤的治疗中取得了良好效果。然而,CAR-T 细胞疗法对实体瘤的疗效已被证明有限,主要原因是肿瘤相关细胞外基质(ECM)为本应杀伤癌细胞的细胞毒性CAR-T 细胞制造了难以逾越的屏障。本综述揭示了肿瘤相关ECM在阻碍CAR-T 细胞向实体瘤内浸润、存活及发挥功能方面的多重作用。
我们分析了肿瘤内ECM作为纯粹物理屏障使淋巴细胞穿透/迁移复杂化,同时也作为免疫抑制因子损害CAR-T 细胞抗肿瘤活性的情况,从而限制CAR-T 细胞疗法疗效。
此外,我们重点介绍了有前景的方法,如工程化改造CAR-T 细胞以增强其穿透和迁移进入/穿过肿瘤内ECM的能力、旨在减弱肿瘤内ECM高密度和免疫抑制潜能的联合疗法,以及其他能够克服ECM相关障碍的方法。对相关研究数据的详细概述不仅有助于更好地理解CAR-T 细胞与肿瘤内ECM之间的相互作用,也勾勒出更有效利用CAR-T 细胞疗法对抗实体瘤的潜在途径。
Chimeric antigen receptor (CAR)-T cell therapy yields good results in the treatment of various hematologic malignancies.
However, the efficacy of CAR-T cell therapy against solid tumors has proven to be limited, primarily because the tumor-associated extracellular matrix (ECM) creates an intractable barrier for the cytotoxic CAR-T cells that are supposed to kill cancer cells. This review unravels the multifaceted role of the tumor-associated ECM in impeding CAR-T cell infiltration, survival, and functions within solid tumors.
We analyze the situations when intratumoral ECM limits the efficacy of CAR-T cell therapy by being a purely physical barrier that complicates lymphocyte penetration/migration and also acts as an immunosuppressive factor that impairs the antitumor activities of CAR-T cells.
In addition, we highlight promising approaches such as engineering CAR-T cells with improved capabilities to penetrate and migrate into/through the intratumoral ECM, combination therapies aimed at attenuating the high density and immunosuppressive potential of the intratumoral ECM, and others that enable overcoming ECM-related obstacles.
A detailed overview of the data of relevant studies not only helps to better understand the interactions between CAR-T cells and the intratumoral ECM but also outlines potential ways to more effectively use CAR-T cell therapy against solid tumors.
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