Sloand Elaine M, Rezvani Katayoun
National Heart Lung and Blood Institute, Hematology Branch, Bethesda, MD 20892, USA.
Semin Hematol. 2008 Jan;45(1):39-48. doi: 10.1053/j.seminhematol.2007.11.006.
Patients with myelodysplastic syndrome (MDS) have intrinsic, usually acquired genetic defects in their hematopoietic stem cells, but some others exhibit T-cell-mediated inhibition of hematopoiesis and good responses to immunosuppression. In these cases, MDS shares a similar pathophysiology with aplastic anemia (AA). Here, we review the evidence supporting a role of the immune system in the pathophysiology of MDS and the results of clinical trials of immunosuppressive agents.
骨髓增生异常综合征(MDS)患者的造血干细胞存在内在的、通常是后天获得的基因缺陷,但其他一些患者表现出T细胞介导的造血抑制以及对免疫抑制的良好反应。在这些情况下,MDS与再生障碍性贫血(AA)具有相似的病理生理学。在此,我们综述支持免疫系统在MDS病理生理学中作用的证据以及免疫抑制剂临床试验的结果。