Gmür J, Frick P G, von Felten A
Blut. 1979 Jul;39(1):47-52. doi: 10.1007/BF01008074.
A 26-year-old man with severe aplastic anemia was treated with high-dose Cyclophosphamide followed by the infusion of bone marrow cells from his HLA-identical sister. After initial intake of the graft, rejection ensued by day 46 which was followed by a permanent complete aplasia. After 4 months, bone marrow retransplantation with the same donor was attempted after a more intensive conditioning regimen. This led to permanent engraftment with rapid normalization of the blood counts lasting now for over 12 months. The patient has since remained in excellent clinical condition without signs of graft-versus-host disease.
一名26岁的重症再生障碍性贫血男性患者接受了大剂量环磷酰胺治疗,随后输注了来自其 HLA 配型相同的姐姐的骨髓细胞。在最初植入移植物后,第46天出现排斥反应,随后出现永久性完全再生障碍。4个月后,在采用更强化的预处理方案后,尝试再次使用同一供体进行骨髓移植。这导致了永久性植入,血细胞计数迅速恢复正常,至今已持续超过12个月。此后,患者一直处于良好的临床状态,没有移植物抗宿主病的迹象。