Fesnak Andrew, Lin ChieYu, Siegel Don L, Maus Marcela V
Division of Transfusion Medicine & Therapeutic Pathology, Department of Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.
Transfus Med Rev. 2016 Jul;30(3):139-45. doi: 10.1016/j.tmrv.2016.03.001. Epub 2016 Mar 28.
The use of chimeric antigen receptor (CAR)-T cell therapy for the treatment of hematologic malignancies has generated significant excitement over the last several years. From a transfusion medicine perspective, the implementation of CAR-T therapy as a potential mainstay treatment for not only hematologic but also solid-organ malignancies represents a significant opportunity for growth and expansion. In this review, we will describe the rationale for the development of genetically redirected T cells as a cancer therapeutic, the different elements that are required to engineer these cells, as well as an overview of the process by which patient cells are harvested and processed to create and subsequently validate CAR-T cells. Finally, we will briefly describe some of the toxicities and clinical efficacy of CAR-T cells in the setting of patients with advanced malignancy.
在过去几年中,嵌合抗原受体(CAR)-T细胞疗法用于治疗血液系统恶性肿瘤引起了极大的关注。从输血医学的角度来看,CAR-T疗法不仅作为血液系统恶性肿瘤而且作为实体器官恶性肿瘤的潜在主要治疗方法的应用,代表了一个显著的增长和扩展机会。在这篇综述中,我们将描述将基因重定向T细胞开发为癌症治疗方法的基本原理、改造这些细胞所需的不同元件,以及患者细胞的采集和处理过程概述,以创建并随后验证CAR-T细胞。最后,我们将简要描述CAR-T细胞在晚期恶性肿瘤患者中的一些毒性和临床疗效。