Wang Xiuyan, Rivière Isabelle
Cell Therapy and Cell Engineering Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Center for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Mol Ther Methods Clin Dev. 2017 Mar 18;5:96-105. doi: 10.1016/j.omtm.2017.03.003. eCollection 2017 Jun 16.
The marketing approval of genetically engineered hematopoietic stem cells (HSCs) as the first-line therapy for the treatment of severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID) is a tribute to the substantial progress that has been made regarding HSC engineering in the past decade. Reproducible manufacturing of high-quality, clinical-grade, genetically engineered HSCs is the foundation for broadening the application of this technology. Herein, the current state-of-the-art manufacturing platforms to genetically engineer HSCs as well as the challenges pertaining to production standardization and product characterization are addressed in the context of primary immunodeficiency diseases (PIDs) and other monogenic disorders.
基因工程造血干细胞(HSCs)作为治疗腺苷脱氨酶缺乏所致重症联合免疫缺陷(ADA - SCID)的一线疗法获得上市批准,这体现了过去十年间HSC工程领域取得的重大进展。可重复生产高质量、临床级的基因工程HSCs是扩大该技术应用的基础。本文在原发性免疫缺陷病(PIDs)和其他单基因疾病的背景下,探讨了目前用于基因工程改造HSCs的先进制造平台,以及与生产标准化和产品特性相关的挑战。