血液学中的嵌合抗原受体T细胞疗法。
Chimeric Antigen Receptor T Cell Therapy in Hematology.
作者信息
Ataca Pınar, Arslan Önder
机构信息
Ankara University Faculty of Medicine, Department of Hematology, Ankara, Turkey E-mail:
出版信息
Turk J Haematol. 2015 Dec;32(4):285-94. doi: 10.4274/tjh.2015.0049. Epub 2015 Aug 6.
It is well demonstrated that the immune system can control and eliminate cancer cells. Immune-mediated elimination of tumor cells has been discovered and is the basis of both cancer vaccines and cellular therapies including hematopoietic stem cell transplantation. Adoptive T cell transfer has been improved to be more specific and potent and to cause less off-target toxicity. Currently, there are two forms of engineered T cells being tested in clinical trials: T cell receptor (TCR) and chimeric antigen receptor (CAR) modified T cells. On 1 July 2014, the United States Food and Drug Administration granted 'breakthrough therapy' designation to anti-CD19 CAR T cell therapy. Many studies were conducted to evaluate the benefits of this exciting and potent new treatment modality. This review summarizes the history of adoptive immunotherapy, adoptive immunotherapy using CARs, the CAR manufacturing process, preclinical and clinical studies, and the effectiveness and drawbacks of this strategy.
充分证明免疫系统能够控制并消除癌细胞。免疫介导的肿瘤细胞消除已被发现,并且是癌症疫苗和包括造血干细胞移植在内的细胞疗法的基础。过继性T细胞转移已得到改进,变得更具特异性和效力,且脱靶毒性更小。目前,有两种形式的工程化T细胞正在临床试验中进行测试:T细胞受体(TCR)和嵌合抗原受体(CAR)修饰的T细胞。2014年7月1日,美国食品药品监督管理局授予抗CD19 CAR T细胞疗法“突破性疗法”认定。开展了许多研究以评估这种令人兴奋且有效的新治疗方式的益处。本综述总结了过继性免疫疗法的历史、使用CAR的过继性免疫疗法、CAR的制造过程、临床前和临床研究,以及该策略的有效性和缺点。