Bone Marrow Transplantation Center-Hematology I, Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, University of Milan, Via Francesco Sforza 35, Milan, Italy.
Expert Rev Hematol. 2009 Dec;2(6):699-715. doi: 10.1586/ehm.09.60.
The term 'autoimmune diseases' encompasses a spectrum of diseases whose clinical manifestations and, possibly, biological features vary widely. The results of conventional treatment are considered unsatisfactory in aggressive forms, with subsets of patients having short life expectancies. Relying on wide experimental evidence and more feeble clinical data, some research groups have used autologous hematopoietic stem cell transplantation (HSCT) in the most disabling autoimmune diseases with the aim of resetting the patient's immune system. Immunoablative conditioning regimens are preferred over their myeloablative counterparts, and some form of in vivo and/or ex vivo T-cell depletion is generally adopted. Despite 15 years' experience, published controlled clinical trials are still lacking, with the evidence so far available coming from pilot studies and registry surveys. In multiple sclerosis, clinical improvement, or at least lasting disease stabilization, can be achieved in the majority of the patients; nevertheless, the worst results are observed in patients with progressive disease, where no benefit can be expected from conventional therapy. Concerning rheumatologic diseases, wide experience has been acquired in systemic sclerosis, with long-term improvements in cutaneous disease being frequently reported, although visceral involvement remains unchanged at best. Autografting has proved to be barely effective in rheumatoid arthritis and quite toxic in juvenile idiopathic arthritis, whereas it leads to clinical remission and the reversal of visceral impairment in the majority of patients with systemic lupus erythematosus. A promising indication is Crohn's disease, in which long-term endoscopic remission is frequently observed. Growing experience with autologous HCST in autoimmune diseases has progressively reduced concerns about transplant-related mortality and secondary myelodysplasia/leukemia. Therefore, a sustained complete remission seems to be within the reach of autografting in some autoimmune diseases; in others, the indications, risks and benefits of autografting need to be better defined. Consequently, the search for new drugs should also be encouraged.
“自身免疫性疾病”这一术语涵盖了一系列疾病,其临床表现和(可能)生物学特征差异很大。在侵袭性形式中,常规治疗的效果不理想,某些患者亚组的预期寿命较短。一些研究小组依靠广泛的实验证据和较弱的临床数据,在最具破坏性的自身免疫性疾病中使用自体造血干细胞移植(HSCT),旨在重置患者的免疫系统。免疫消融预处理方案优于其骨髓消融对应方案,并且通常采用某种形式的体内和/或体外 T 细胞耗竭。尽管有 15 年的经验,但仍缺乏已发表的对照临床试验,迄今为止,可用的证据来自于试点研究和登记调查。在多发性硬化症中,大多数患者可以实现临床改善,或至少持久的疾病稳定,但在进行性疾病患者中观察到最糟糕的结果,常规治疗对此类患者无效。在风湿性疾病方面,系统性硬化症积累了广泛的经验,经常报道皮肤疾病的长期改善,尽管内脏受累最好也只是保持不变。自体移植在类风湿关节炎中几乎没有效果,在幼年特发性关节炎中毒性较大,但在大多数系统性红斑狼疮患者中,它可导致临床缓解和内脏损害逆转。克罗恩病是一个有前景的适应证,在该疾病中,经常观察到长期的内镜缓解。自身免疫性疾病中自体 HSCT 的经验不断增加,逐渐减少了对移植相关死亡率和继发性骨髓增生异常/白血病的担忧。因此,在某些自身免疫性疾病中,自体移植似乎可以达到持续完全缓解;而在其他疾病中,自体移植的适应证、风险和益处需要进一步明确。因此,也应鼓励寻找新的药物。