决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:TCR engineered T cells for solid tumor immunotherapy.
T 细胞免疫治疗仍是肿瘤免疫治疗中颇具吸引力的一种方法。
T 细胞免疫疗法仍是癌症免疫治疗中有吸引力的方法,主要采用嵌合抗原受体(CAR)和 T 细胞受体(TCR)工程化 T 细胞。CAR-T 细胞疗法是治疗血液系统恶性肿瘤的重要突破。TCR-T 细胞能够识别表达于细胞表面和细胞内区室的抗原。虽然 TCR-T 尚未获批临床应用,但已开展多项临床试验,尤其针对实体瘤。本文总结 TCR-T 细胞的当前进展及其在实体瘤免疫治疗中的潜在优势。
T cell immunotherapy remains an attractive approach for cancer immunotherapy. T cell immunotherapy mainly employs chimeric antigen receptor (CAR)- and T cell receptor (TCR)-engineered T cells. CAR-T cell therapy has been an essential breakthrough in treating hematological malignancies. TCR-T cells can recognize antigens expressed both on cell surfaces and in intracellular compartments. Although TCR-T cells have not been approved for clinical application, a number of clinical trials have been performed, particularly for solid tumors. In this article, we summarized current TCR-T cell advances and their potential advantages for solid tumor immunotherapy.
MEMBER ACCOUNT
登录成功会直接打开下一页。