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The role of autologous haemopoietic stem cell transplantation in the treatment of autoimmune disorders

机译:自体造血干细胞移植在自身免疫性疾病治疗中的作用

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摘要

Autologous haemopoietic stem cell transplantation (HSCT) has been used for over 30years for malignant haematological diseases, such as myeloma and lymphoma, with considerable success. More recently this procedure has been adopted as a form of high dose immunosuppression in selected patients with autoimmune diseases that are resistant to conventional therapies. Animal models have previously outlined the rationale and validity of HSCT in patients with these non-malignant, but in many cases, life-threatening conditions. Recent data have that deletion of putative autoreactive immune clones with reconstitution of a thymic driven, tolerant immune system occurs in HSCT for auto-immune patients. Two randomised control trials have confirmed that HSCT is superior to monthly cyclophosphamide in systemic sclerosis with a highly significant disease free and overall survival benefit demonstrated in the Autologous Stem cell Transplantation International Scleroderma trial. Over 2000 patients worldwide with autoimmune conditions have been treated with HSCT - the commonest indications being multiple sclerosis (MS) and systemic sclerosis. Encouraging relapse free survival of 70-80% at 4years, in heavily pre-treated MS patients, has been demonstrated in Phase II trials. A Phase III trial in MS patients who have failed interferon is currently accruing patients. Future challenges include improvements in safety of HSCT, particularly in cardiac assessment of systemic sclerosis patients, cost-benefit analyses of HSCT compared to standard therapy and establishment of centres of excellence to continue to enhance the safety and benefit of this exciting new therapy.
机译:自体造血干细胞移植(HSCT)在恶性血液病(如骨髓瘤和淋巴瘤)中已使用了30多年,取得了巨大的成功。最近,该方法已被采用为对常规疗法有抵抗力的某些自身免疫性疾病患者的高剂量免疫抑制形式。动物模型先前已经概述了这些非恶性肿瘤但在许多情况下危及生命的患者中HSCT的原理和有效性。最近的数据表明,对于自体免疫患者,HSCT发生了胸腺驱动的耐受性免疫系统的重建,从而推定了自身反应性免疫克隆的缺失。两项随机对照试验已证实,在系统性硬化症中,HSCT优于每月环磷酰胺,并且在国际自体干细胞移植硬皮病试验中显示出高度无疾病的显着的总体生存优势。 HSCT治疗了全球超过2000名自身免疫性疾病的患者-最常见的适应症是多发性硬化症(MS)和全身性硬化症。 II期试验已证明,在接受大量预处理的MS患者中,鼓励4年内70-80%的无复发存活率是可行的。干扰素治疗失败的MS患者的一项III期试验目前正在招募患者。未来的挑战包括改善HSCT的安全性,特别是系统性硬化症患者的心脏评估,与标准疗法相比的HSCT成本效益分析以及建立卓越中心以继续提高这种令人振奋的新疗法的安全性和益处。

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