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用于治疗遗传性疾病的造血干细胞移植

Haemopoietic stem cell transplantation for genetic disorders.

作者信息

Steward C G, Jarisch A

机构信息

Bone Marrow Transplant Unit, Royal Hospital for Children, Bristol, UK.

出版信息

Arch Dis Child. 2005 Dec;90(12):1259-63. doi: 10.1136/adc.2005.074278.

Abstract

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.

摘要

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。

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本文引用的文献

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Br J Haematol. 2005 Apr;129(2):178-88. doi: 10.1111/j.1365-2141.2004.05351.x.
2
Late effects after stem cell transplantation (SCT) in children--growth and hormones.
Bone Marrow Transplant. 2005 Mar;35 Suppl 1:S77-81. doi: 10.1038/sj.bmt.1704853.
5
Hemopoietic chimerism following stem cell transplantation.干细胞移植后的造血嵌合现象。
Transfus Apher Sci. 2005 Feb;32(1):55-61. doi: 10.1016/j.transci.2004.10.006.
6
Lysosomal storage disorders.溶酶体贮积症
Br J Haematol. 2005 Feb;128(4):413-31. doi: 10.1111/j.1365-2141.2004.05293.x.
7
Pathogenesis of graft-versus-host-disease.移植物抗宿主病的发病机制。
Biol Blood Marrow Transplant. 2005 Feb;11(2 Suppl 2):21-3. doi: 10.1016/j.bbmt.2004.11.003.
9
Osteopetrosis.骨质石化症
N Engl J Med. 2004 Dec 30;351(27):2839-49. doi: 10.1056/NEJMra040952.
10
Cytomegalovirus following stem cell transplantation: from pharmacologic to immunologic therapy.
Expert Rev Anti Infect Ther. 2004 Aug;2(4):559-73. doi: 10.1586/14787210.2.4.559.

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