Tyndall Alan, Furst Daniel E
Department of Rheumatology, University of Basel, Switzerland.
Curr Opin Rheumatol. 2007 Nov;19(6):604-10. doi: 10.1097/BOR.0b013e3282e6f534.
Provides an update of hematopoietic stem cell transplantation for systemic sclerosis from phase I/II studies and prospective randomized phase III trials, and introduces the concept of mesenchymal stem cells as potential therapy for autoimmune disease.
Around 170 transplanted systemic sclerosis patients are registered in Europe. Most received autologous, peripheral blood derived hematopoietic stem cell transplantation. Treatment-related mortality has fallen to 2.5% in the controlled trials compared with 12.5% in the first report in 2002. Over one-third of patients have experienced sustained remission. Two prospective randomized phase III studies are active: the Autologous Stem cell Transplantation International Scleroderma (ASTIS) trial in Europe and the Scleroderma Cyclophosphamide Or Transplant (SCOT) trial in the USA. Both have similar selection criteria, endpoint and control arms, but the SCOT trial uses radiation and less cyclophosphamide. So far, no unexpected toxicity has occurred. Reports produced in the past 12 months show reduction of skin collagen and reversal of microvascular remodelling, years after transplant. Bone marrow-derived mesenchymal stem cells from systemic sclerosis patients show in-vitro immunomodulatory properties equal to healthy controls.
Hematopoietic stem cell transplantation is currently being tested in prospective randomized controlled trials and appears to 'reset' autoimmunity in systemic sclerosis. Mesenchymal stem cells may have an immunomodulatory role in autoimmune disease.
介绍来自I/II期研究及前瞻性随机III期试验的系统性硬化症造血干细胞移植的最新情况,并引入间充质干细胞作为自身免疫性疾病潜在治疗方法的概念。
欧洲登记了约170例接受移植的系统性硬化症患者。大多数患者接受了自体外周血来源的造血干细胞移植。与2002年首份报告中的12.5%相比,对照试验中与治疗相关的死亡率已降至2.5%。超过三分之一的患者实现了持续缓解。两项前瞻性随机III期研究正在进行:欧洲的自体干细胞移植国际硬皮病(ASTIS)试验和美国的硬皮病环磷酰胺或移植(SCOT)试验。两者具有相似的选择标准、终点和对照臂,但SCOT试验使用放疗且环磷酰胺用量较少。到目前为止,未出现意外毒性。过去12个月发布的报告显示,移植多年后皮肤胶原蛋白减少且微血管重塑逆转。系统性硬化症患者的骨髓来源间充质干细胞在体外显示出与健康对照相当的免疫调节特性。
造血干细胞移植目前正在前瞻性随机对照试验中进行测试,似乎能在系统性硬化症中“重置”自身免疫。间充质干细胞可能在自身免疫性疾病中具有免疫调节作用。