Bhattacharya Deepta, Ehrlich Lauren I Richie, Weissman Irving L
Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5323, USA.
Eur J Immunol. 2008 Aug;38(8):2060-7. doi: 10.1002/eji.200838383.
The mammalian blood system contains a multitude of distinct mature cell lineages adapted to serving diverse functional roles. Mutations that abrogate the development or function of one or more of these lineages can lead to profound adverse consequences, such as immunodeficiency, autoimmunity, or anemia. Replacement of hematopoietic stem cells (HSC) that carry such mutations with HSC from a healthy donor can reverse such disorders, but because the risks associated with the procedure are often more serious than the blood disorders themselves, bone marrow transplantation is generally not used to treat a number of relatively common inherited blood diseases. Aside from a number of other problems, risks associated with cytoreductive treatments that create "space" for donor HSC, and the slow kinetics with which immune competence is restored following transplantation hamper progress. This review will focus on how recent studies using experimental model systems may direct future efforts to implement routine use of HSC transplantation to cure inherited blood disorders.
哺乳动物的血液系统包含众多不同的成熟细胞谱系,这些谱系适应于发挥多种功能作用。消除这些谱系中一个或多个谱系的发育或功能的突变会导致严重的不良后果,如免疫缺陷、自身免疫或贫血。用健康供体的造血干细胞(HSC)替代携带此类突变的造血干细胞可以逆转此类疾病,但由于该手术相关的风险通常比血液疾病本身更严重,骨髓移植一般不用于治疗一些相对常见的遗传性血液疾病。除了许多其他问题外,与为供体造血干细胞创造“空间”的细胞减灭治疗相关的风险,以及移植后免疫能力恢复的缓慢动力学阻碍了进展。本综述将重点关注近期使用实验模型系统的研究如何指导未来的努力,以实现常规使用造血干细胞移植来治愈遗传性血液疾病。