Department of Medical Oncology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, United States.
Front Immunol. 2023 Sep 1;14:1237782. doi: 10.3389/fimmu.2023.1237782. eCollection 2023.
Allogeneic hematopoietic stem cell transplantation (HSCT) provides the only potentially curative option for multiple hematological conditions. However, allogeneic HSCT outcomes rely on an optimal balance of effective immune recovery, minimal graft-versus-host disease (GVHD), and lasting control of disease. The quest to attain this balance has proven challenging over the past few decades. The two-step approach to HSCT was conceptualized and pioneered at Thomas Jefferson University in 2005 and remains the main platform for allografting at our institution. Following administration of the transplant conditioning regimen, patients receive a fixed dose of donor CD3+ cells (HSCT step one-DLI) as the lymphoid portion of the graft on day -6 with the aim of optimizing and controlling T cell dosing. Cyclophosphamide (CY) is administered after the DLI (days -3 and -2) to induce donor-recipient bidirectional tolerance. On day 0, a CD34-selected stem cell graft is given as the myeloid portion of the graft (step two). In this two-step approach, the stem cell graft is infused after CY tolerization, which avoids exposure of the stem cells to an alkylating agent, allowing rapid count recovery. Here, the two-step platform is described with a focus on key results from studies over the past two decades. Finally, this review details lessons learned and current strategies to optimize the graft-versus-tumor effect and limit transplant-related toxicities.
异基因造血干细胞移植 (HSCT) 为多种血液系统疾病提供了唯一潜在的治愈选择。然而,异基因 HSCT 的结果依赖于有效免疫恢复、最小的移植物抗宿主病 (GVHD) 和疾病持续控制之间的最佳平衡。在过去的几十年中,人们一直在努力实现这一平衡。两步法 HSCT 于 2005 年在托马斯杰斐逊大学提出并首创,至今仍是我们机构同种异体移植的主要平台。在移植预处理方案给药后,患者在第 -6 天接受固定剂量的供体 CD3+细胞 (HSCT 第一步-DLI) 作为移植物的淋巴细胞部分,目的是优化和控制 T 细胞剂量。在 DLI 后 (第 -3 天和 -2 天) 给予环磷酰胺 (CY) 以诱导供受者双向耐受。在第 0 天,给予 CD34 分选的干细胞作为移植物的髓系部分 (第二步)。在两步法中,在 CY 耐受后输注干细胞移植,这避免了干细胞暴露于烷化剂,从而实现快速计数恢复。在此,重点介绍了过去二十年的研究中的关键结果,描述了两步法平台。最后,本文详细介绍了优化移植物抗肿瘤效应和限制移植相关毒性的经验教训和当前策略。