Dana-Farber Cancer Institute, Boston, MA;
Blood. 2013 Oct 24;122(17):3074-81. doi: 10.1182/blood-2013-05-503177. Epub 2013 Aug 30.
Umbilical cord blood (UCB) is a valuable source of hematopoietic stem cells (HSCs) for use in allogeneic transplantation. Key advantages of UCB are rapid availability and less stringent requirements for HLA matching. However, UCB contains an inherently limited HSC count, which is associated with delayed time to engraftment, high graft failure rates, and early mortality. 16,16-Dimethyl prostaglandin E2 (dmPGE2) was previously identified to be a critical regulator of HSC homeostasis, and we hypothesized that brief ex vivo modulation with dmPGE2 could improve patient outcomes by increasing the "effective dose" of HSCs. Molecular profiling approaches were used to determine the optimal ex vivo modulation conditions (temperature, time, concentration, and media) for use in the clinical setting. A phase 1 trial was performed to evaluate the safety and therapeutic potential of ex vivo modulation of a single UCB unit using dmPGE2 before reduced-intensity, double UCB transplantation. Results from this study demonstrated clear safety with durable, multilineage engraftment of dmPGE2-treated UCB units. We observed encouraging trends in efficacy, with accelerated neutrophil recovery (17.5 vs 21 days, P = .045), coupled with preferential, long-term engraftment of the dmPGE2-treated UCB unit in 10 of 12 treated participants.
脐带血 (UCB) 是异体移植中造血干细胞 (HSCs) 的宝贵来源。UCB 的主要优势在于其快速可用性和对 HLA 匹配要求较低。然而,UCB 中 HSC 的固有数量有限,这与植入延迟、高移植物失败率和早期死亡率有关。16,16-二甲基前列腺素 E2 (dmPGE2) 先前被确定为 HSC 动态平衡的关键调节因子,我们假设通过增加 HSCs 的“有效剂量”,短暂的体外 dmPGE2 调节可以改善患者的预后。采用分子谱分析方法确定了用于临床的最佳体外调节条件(温度、时间、浓度和培养基)。进行了一项 I 期试验,以评估在减少强度、双脐带血移植前使用 dmPGE2 体外调节单个脐带血单位的安全性和治疗潜力。这项研究的结果表明,dmPGE2 处理的脐带血单位具有明显的安全性,可实现持久的多谱系植入。我们观察到在疗效方面有令人鼓舞的趋势,中性粒细胞恢复加速(17.5 天 vs 21 天,P =.045),同时 dmPGE2 处理的脐带血单位在 12 名接受治疗的参与者中有 10 名优先、长期植入。