Passweg Jakob, Tyndall Alan
Division of Hematology, University Hospital Geneva, Geneva, Switzerland.
Semin Hematol. 2007 Oct;44(4):278-85. doi: 10.1053/j.seminhematol.2007.08.001.
Since 1996, approximately 1,000 patients have received an autologous hematopoietic stem cell transplant (HSCT) as treatment for a severe autoimmune disease (AD). The European Group for Blood and Marrow Transplantation (EBMT)/European League Against Rheumatism (EULAR) Autoimmune Disease Working Party have registered more than 800 patients and works in close collaboration with networks in the United States where several hundred more AD patients have been similarly transplanted. The majority of ADs were multiple sclerosis (MS), systemic sclerosis (SSc), systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), juvenile idiopathic arthritis, and immune cytopenias. Many patients have experienced long-term disease-free remissions and immune reconstitution studies have shown in some cases that a "resetting" of autoimmunity is possible. The initially high treatment-related mortality (TRM) is reduced significantly in the later years, and the phase I/II experience is now being verified in several international prospective randomized clinical trials. In addition, the past several years have seen a growing interest in the role and potential therapeutic application of mesenchymal stem cells (MSC) in the immunomodulation of AD, as in the early experience with acute-graft-versus host disease (GvHD).
自1996年以来,约1000例患者接受了自体造血干细胞移植(HSCT),作为严重自身免疫性疾病(AD)的治疗手段。欧洲血液和骨髓移植组(EBMT)/欧洲抗风湿病联盟(EULAR)自身免疫性疾病工作组已登记了800多名患者,并与美国的相关网络密切合作,在美国又有数百名AD患者接受了类似移植。大多数自身免疫性疾病为多发性硬化症(MS)、系统性硬化症(SSc)、系统性红斑狼疮(SLE)、类风湿关节炎(RA)、幼年特发性关节炎和免疫性血细胞减少症。许多患者实现了长期无病缓解,免疫重建研究在某些情况下表明自身免疫“重置”是可能的。最初较高的治疗相关死亡率(TRM)在后期显著降低,目前一些国际前瞻性随机临床试验正在验证I/II期的经验。此外,过去几年间,间充质干细胞(MSC)在自身免疫性疾病免疫调节中的作用和潜在治疗应用越来越受到关注,就如同急性移植物抗宿主病(GvHD)的早期经验一样。