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[干细胞治疗自身免疫性疾病]

[Stem cell treatment of autoimmune disease].

作者信息

Daikeler T, Tyndall A

机构信息

Rheumatologische Universitätsklinik, Basel.

出版信息

Dtsch Med Wochenschr. 2011 Aug;136(33):1684-6. doi: 10.1055/s-0031-1286063. Epub 2011 Aug 10.

Abstract

Over 1,500 patients world wide have received a hematopoietic stem cell transplant (HSCT) as treatment for a severe autoimmune disease. Most of these have been autologous and mostly have occurred in the past 15 years. Over 1,000 of these have been registered in the European Group for Bone Marrow Transplantation (EBMT) and European League Against Rheumatism (EULAR) combined data base. A recent retrospective analysis of 900 patients (1) showed that the majority had multiple sclerosis (n = 345) followed by systemic sclerosis (n = 175), systemic lupus erythematosus (n = 85), rheumatoid arthritis (n = 89), juvenile idiopathic arthritis (n = 65) and idiopathic cytopenic purpura (n = 37). An overall 85 % 5-year-survival and 43 % progression-free survival was seen, with 100-day-transplant-related-mortality (TRM) ranging between 1 % (rheumatoid arthritis) and 11 % (systemic lupus erythematosus and juvenile idiopathic arthritis). Around 30 % of patients in all disease subgroups had a complete response, often durable despite full immune reconstitution. In many, e. g. systemic sclerosis, morphological improvement such as reduction of skin collagen and normalisation of microvasculature was documented, beyond any predicted known effects of intense immunosuppression alone. The high TRM was in part related to conditioning intensity, comorbidity and age, and the final risk/benefit assessment will be made after the results of the three randomised propective clinical trials are known. [nl]Recently, multipotent mesenchymal stromal cells have been tested in various autoimmune diseases, exploiting their immune modulating properties and apparent low acute toxicity. Despite encouraging small phase I/II studies, no positive data from randomised, prospective studies are as yet available in the peer reviewed literature.

摘要

全球已有超过1500名患者接受了造血干细胞移植(HSCT),作为一种严重自身免疫性疾病的治疗方法。其中大多数是自体移植,且大多发生在过去15年。这些患者中有1000多名已被登记在欧洲骨髓移植组(EBMT)和欧洲抗风湿病联盟(EULAR)的联合数据库中。最近一项对900名患者的回顾性分析(1)显示,大多数患者患有多发性硬化症(n = 345),其次是系统性硬化症(n = 175)、系统性红斑狼疮(n = 85)、类风湿性关节炎(n = 89)、幼年特发性关节炎(n = 65)和特发性血细胞减少性紫癜(n = 37)。总体5年生存率为85%,无进展生存率为43%,移植相关死亡率(TRM)在100天内介于1%(类风湿性关节炎)和11%(系统性红斑狼疮和幼年特发性关节炎)之间。所有疾病亚组中约30%的患者有完全缓解,尽管免疫功能完全重建,但通常持久。在许多疾病中,例如系统性硬化症,记录到了形态学改善,如皮肤胶原蛋白减少和微血管正常化,这超出了仅强烈免疫抑制的任何预期已知效果。高TRM部分与预处理强度、合并症和年龄有关,最终的风险/效益评估将在三项随机前瞻性临床试验结果知晓后进行。[荷兰语]最近,多能间充质基质细胞已在各种自身免疫性疾病中进行了测试,利用了它们的免疫调节特性和明显较低的急性毒性。尽管小型I/II期研究令人鼓舞,但同行评审文献中尚无随机前瞻性研究的阳性数据。

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