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Haemopoietic stem cell transplantation for genetic disorders.

机译:用于遗传疾病的造血干细胞移植。

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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.
机译:干细胞移植(SCT)用于治疗或大大改善各种遗传疾病,从造血细胞生产或功能的固有缺陷到主要影响实体器官的代谢疾病。它被视为过去40年中最杰出的治疗进展之一。尽管技术发展迅速,但是仍然存在许多短期风险和潜在的长期毒性。结果,替代疗法(包括新药,酶和基因疗法)的迅速出现,使得需要不断重新评估每种疾病的风险/获益比,从而需要重新评估SCT的适用性。这篇综述描述了移植过程的主要方面,移植适应症,结果统计数据以及可供选择的替代疗法领域。

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