Niu Jing-Wen, Hu Jiangwei, Chen Hu, Zhang Bin, Hu Liangding
Senior Department of Hematology, the Fifth Medical Center of PLA General Hospital, N0.8 Dongda Street, Fengtai District, Beijing, China.
Stem Cell Res Ther. 2025 Feb 10;16(1):61. doi: 10.1186/s13287-024-04119-y.
Fetal liver hematopoietic stem cells (HSCs) have the capacity to temporarily engraft, thereby facilitating the reconstitution of hematopoiesis without severe graft-versus-host disease (GVHD). In two cases of acute leukemia, the patients underwent fetal liver transplantation (FLT), receiving cells from multiple donors at doses ranging from 7.02 to 8.3 × 10^8 cells/kg, following an intensive conditioning regimen in 1983 and 1985. Remarkably, both individuals have since achieved sustained complete remission and hematopoietic recovery, and have maintained a normal life for over three decades. Although FLT is no longer a viable clinical option, the positive outcomes of these cases are noteworthy and are shared herein. Our findings underscore the potential of FLT to offer short-term hematopoietic support, contributing to the recovery of patients with acute leukemia and may inspire research into ideal HSCs that emulate the characteristics of fetal liver cells for future transplantation applications.
胎儿肝脏造血干细胞(HSCs)具有暂时植入的能力,从而有助于在无严重移植物抗宿主病(GVHD)的情况下重建造血功能。在两例急性白血病患者中,这两名患者于1983年和1985年接受了胎儿肝脏移植(FLT),在强化预处理方案后,接受了来自多个供体的细胞,剂量范围为7.02至8.3×10^8个细胞/千克。值得注意的是,自那以后,这两名患者均实现了持续完全缓解和造血恢复,并维持了三十多年的正常生活。尽管胎儿肝脏移植已不再是可行的临床选择,但这些病例的积极结果值得关注,并在此分享。我们的研究结果强调了胎儿肝脏移植提供短期造血支持的潜力,有助于急性白血病患者的康复,并可能激发对模仿胎儿肝脏细胞特征的理想造血干细胞的研究,以供未来移植应用。