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:Rewiring immunity with in vivo CAR T cell engineering.
我们以转化展望作结,既强调机遇,也指出那些将决定临床实施路径的悬而未决的问题。
离体工程化嵌合抗原受体(CAR)T 细胞疗法已改变某些血液系统恶性肿瘤的治疗,但生产流程复杂、患者可及性有限,制约了其影响范围。体内 CAR-T 细胞工程旨在直接在个体体内生成 CAR-T 细胞,以克服这些限制。本文展望肿瘤领域快速发展的体内 CAR-T 细胞生成研究,概述淋巴细胞靶向原则,讨论药理学特征和生物分布,并评估新出现的安全性问题。最后,我们从转化研究角度展望该领域,重点指出其机遇以及决定临床应用路径的待解问题。
Ex vivo engineered chimeric antigen receptor (CAR) T cell therapy has transformed the treatment of certain hematologic malignancies, yet manufacturing complexities and limited patient accessibility constrain its impact. In vivo CAR T cell engineering seeks to overcome these limitations by generating CAR T cells directly within an individual. This Perspective examines the rapidly evolving field of in vivo CAR T cell generation in oncology, outlines principles of lymphocyte targeting, discusses pharmacology and biodistribution and assesses emerging safety issues. We conclude with a translational outlook, highlighting both the opportunities and the outstanding questions that will define the path to clinical implementation.
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