Burt R K, Marmont A, Schroeder J, Rosa R, Traynor A E
Northwestern University Medical Center, The Robert H. Lurie Cancer Center, Chicago, Illinois, USA.
J Clin Immunol. 2000 Jan;20(1):31-7. doi: 10.1023/a:1006638510160.
The treatment of severe autoimmune diseases has been recently revitalized by the introduction of intense immune suppression with immune ablative intent followed by three different procedures. These are allogeneic hematopoietic stem cell transplantation (HSCT), autologous HSCT (using either marrow or peripheral blood), and intense immune suppression without stem cell support. Current trials suggest that high dose immune suppressive therapy with or without autologous hematopoietic stem cell support can induce remission of previously refractory disease. Follow-up is too brief to determine if intense immune suppression, and more specifically autologous HSCT, will ultimately cure SLE. It is conceivable that an allogeneic source of stem cells from a normal donor (e.g. HLA matched sibling) will be required to achieve a cure. It is also possible that autologous HSCT, even if not curative, may prolong the life of patients with otherwise high-risk features. In carefully selected patients, the potential benefits of this procedure may outweigh the risks.
最近,通过引入具有免疫清除意图的强化免疫抑制并随后采用三种不同程序,严重自身免疫性疾病的治疗得以重振。这三种程序分别是异基因造血干细胞移植(HSCT)、自体HSCT(使用骨髓或外周血)以及无干细胞支持的强化免疫抑制。目前的试验表明,无论有无自体造血干细胞支持,高剂量免疫抑制疗法均可诱导先前难治性疾病的缓解。随访时间过短,无法确定强化免疫抑制,尤其是自体HSCT,最终能否治愈系统性红斑狼疮(SLE)。可以想象,可能需要来自正常供体(如人类白细胞抗原(HLA)匹配的同胞)的异基因干细胞来源才能实现治愈。即使自体HSCT不能治愈,也有可能延长具有其他高风险特征患者的生命。在精心挑选的患者中,该程序的潜在益处可能超过风险。