Steward C G, Jarisch A
Bone Marrow Transplant Unit, Royal Hospital for Children, Bristol, UK.
Arch Dis Child. 2005 Dec;90(12):1259-63. doi: 10.1136/adc.2005.074278.
Stem cell transplantation (SCT) is used to cure or greatly ameliorate a wide variety of genetic diseases, ranging from inherent defects of haemopoietic cell production or function to metabolic diseases mostly affecting solid organs. It ranks as one of the most remarkable therapeutic advances of the past 40 years. Despite rapid technological improvements, however, there are still many short term risks and potential long term toxicities. As a consequence, the rapid emergence of alternative therapies (including new drugs, enzyme and gene therapies), necessitate constant re-evaluation of the risk/benefit ratio for each disease and hence the appropriateness of SCT. This review describes the major aspects of the transplant process, indications for transplantation, outcome statistics, and areas where alternative therapies are becoming available.
干细胞移植(SCT)用于治愈或极大地改善多种遗传疾病,范围从造血细胞生成或功能的内在缺陷到主要影响实体器官的代谢疾病。它是过去40年中最显著的治疗进展之一。然而,尽管技术迅速进步,但仍存在许多短期风险和潜在的长期毒性。因此,替代疗法(包括新药、酶和基因疗法)的迅速出现,使得有必要不断重新评估每种疾病的风险/效益比,从而确定SCT的适用性。本综述描述了移植过程的主要方面、移植指征、结果统计以及替代疗法可用的领域。