Department of Immunology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 417 E 68th St, New York, NY, 10065, USA; City of Hope National Medical Center, 1500 E Duarte Rd, Duarte, CA, 91010, USA.
City of Hope National Medical Center, 1500 E Duarte Rd, Duarte, CA, 91010, USA.
Best Pract Res Clin Haematol. 2024 Sep;37(3):101566. doi: 10.1016/j.beha.2024.101566. Epub 2024 Jul 25.
Chimeric antigen receptor (CAR) T cell therapy has shown impressive clinical efficacy in B cell malignancies and multiple myeloma, leading to the approval of six CAR T cell products by the U.S. Food and Drug Administration (FDA) to date. However, broad application of these autologous (patient-derived) CAR T cells is limited by several factors, including high production costs, inconsistent product quality, contamination of the cell product with malignant cells, manufacturing failure especially in heavily pre-treated patients, and lengthy manufacturing times resulting in subsequent treatment delay. A potential solution to these barriers lies in the use of allogeneic "off-the-shelf" CAR T cells produced from healthy donors. Many efforts are underway to make allogeneic CAR T cells a safe and efficacious therapeutic option. In this review, we will discuss the major challenges that have to be addressed to successfully develop allogeneic CAR T cell therapies, specifically graft-versus-host disease (GVHD) and host-mediated immune rejection of the donor cells. Furthermore, we will summarize approaches that have been utilized to overcome these limitations, focusing on the use of gene editing technologies and strategies employing alternative cell populations as the source for allogeneic CAR T cell production.
嵌合抗原受体 (CAR) T 细胞疗法在 B 细胞恶性肿瘤和多发性骨髓瘤中显示出令人印象深刻的临床疗效,迄今为止,已有 6 种 CAR T 细胞产品获得美国食品和药物管理局 (FDA) 的批准。然而,这些自体(患者来源)CAR T 细胞的广泛应用受到多种因素的限制,包括生产成本高、产品质量不一致、细胞产品被恶性细胞污染、制造失败(尤其是在预处理过的患者中)以及制造时间长导致后续治疗延迟。解决这些障碍的一个潜在方法是使用来自健康供体的同种异体“现成”CAR T 细胞。目前正在进行许多努力,以使同种异体 CAR T 细胞成为一种安全有效的治疗选择。在这篇综述中,我们将讨论成功开发同种异体 CAR T 细胞疗法所必须解决的主要挑战,特别是移植物抗宿主病 (GVHD) 和宿主对供体细胞的免疫排斥。此外,我们将总结已经利用的方法来克服这些限制,重点关注基因编辑技术的使用和利用替代细胞群体作为同种异体 CAR T 细胞生产来源的策略。