Marmont du Haut Champ Alberto M
Division of Hematology and Stem Cell Transplantation, IRCCS Azienda Ospedaliera Universitaria San Martino-IST, Genoa, Italy.
Clin Dev Immunol. 2012;2012:380391. doi: 10.1155/2012/380391. Epub 2012 Aug 30.
Two streams of research are at the origin of the utilization of hematopoietic stem cell transplantation (HSCT) for severe autoimmune diseases (SADs). The allogeneic approach came from experimental studies on lupus mice, besides clinical results in coincidental diseases. The autologous procedure was encouraged by researches on experimental neurological and rheumatic disorders. At present the number of allogeneic HSCT performed for human SADs can be estimated to not over 100 patients, and the results are not greatly encouraging, considering the significant transplant-related mortality (TRM) and the occasional development of a new autoimmune disorder and/or relapses notwithstanding full donor chimerism. Autologous HSCT for refractory SLE has become a major target. Severe cases have been salvaged, TRM is low and diminishing, and prolonged clinical remissions are obtainable. Two types of immune resetting have been established, "re-education" and regulatory T cell (Tregs) normalization. Allogeneic HSCT for SLE seems best indicated for patients with disease complicated by an oncohematologic malignancy. Autologous HSCT is a powerful salvage therapy for otherwise intractable SLE. The duration of remission in uncertain, but a favorable response to previously inactive treatments is a generally constant feature. The comparison with new biological agents, or the combination of both, are to be ascertained.
造血干细胞移植(HSCT)用于治疗严重自身免疫性疾病(SADs)源于两条研究路线。同种异体移植方法源于对狼疮小鼠的实验研究以及偶发疾病的临床结果。自体移植程序则受到实验性神经和风湿性疾病研究的推动。目前,为人类SADs进行的同种异体HSCT数量估计不超过100例患者,考虑到显著的移植相关死亡率(TRM)以及尽管实现了完全供体嵌合但仍偶尔出现新的自身免疫性疾病和/或复发情况,其结果并不十分令人鼓舞。难治性系统性红斑狼疮(SLE)的自体HSCT已成为主要目标。重症病例得到了挽救,TRM较低且在降低,并且可实现长期临床缓解。已经确立了两种免疫重置方式,即“再教育”和调节性T细胞(Tregs)正常化。SLE的同种异体HSCT似乎最适合伴有血液系统恶性肿瘤的患者。自体HSCT是治疗其他难以治愈的SLE的有效挽救疗法。缓解期持续时间尚不确定,但对先前无效治疗产生良好反应是一个普遍恒定的特征。与新型生物制剂的比较,或两者的联合应用,有待确定。