Themeli Maria, Rivière Isabelle, Sadelain Michel
The Center for Cell Engineering, Immunology and Molecular Pharmacology and Chemistry Programs, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
The Center for Cell Engineering, Immunology and Molecular Pharmacology and Chemistry Programs, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Cell Stem Cell. 2015 Apr 2;16(4):357-66. doi: 10.1016/j.stem.2015.03.011.
The promising clinical results obtained with engineered T cells, including chimeric antigen receptor (CAR) therapy, call for further advancements to facilitate and broaden their applicability. One potentially beneficial innovation is to exploit new T cell sources that reduce the need for autologous cell manufacturing and enable cell transfer across histocompatibility barriers. Here we review emerging T cell engineering approaches that utilize alternative T cell sources, which include virus-specific or T cell receptor-less allogeneic T cells, expanded lymphoid progenitors, and induced pluripotent stem cell (iPSC)-derived T lymphocytes. The latter offer the prospect for true off-the-shelf, genetically enhanced, histocompatible cell therapy products.
工程化T细胞(包括嵌合抗原受体(CAR)疗法)所取得的令人鼓舞的临床结果,要求进一步改进以促进并拓宽其适用性。一项潜在有益的创新是利用新的T细胞来源,以减少对自体细胞制造的需求,并实现跨组织相容性屏障的细胞转移。在此,我们综述了新兴的T细胞工程方法,这些方法利用了替代T细胞来源,包括病毒特异性或无T细胞受体的同种异体T细胞、扩增的淋巴祖细胞以及诱导多能干细胞(iPSC)衍生的T淋巴细胞。后者为真正的现成、基因增强、组织相容性细胞治疗产品提供了前景。