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造血干细胞移植治疗自身免疫性疾病。

Haematopoietic stem cell transplantation for autoimmune diseases.

机构信息

Paediatric Immunology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, 3508 AB Utrecht, Netherlands.

Laboratory of Translational Immunology, University Medical Centre Utrecht, 3508 AB Utrecht, Netherlands.

出版信息

Nat Rev Rheumatol. 2017 Apr;13(4):244-256. doi: 10.1038/nrrheum.2017.7. Epub 2017 Feb 23.

Abstract

Autologous haematopoietic stem cell transplantation (HSCT) is the only treatment that is able to induce long-term, drug-free and symptom-free remission in several refractory autoimmune rheumatic diseases. Over 3,000 HSCT procedures for rheumatic and nonrheumatic severe autoimmune diseases have been performed worldwide. Specific conditioning regimens are currently used to eradicate the autoreactive immunological memory of patients. Although in vivo immune cell depletion with antithymocyte globulin or anti-CD52 is the norm for many regimens, ex vivo selection of CD34 stem cells from the graft is controversial. Following the extensive immune depletion associated with serotherapy and chemotherapy, HSCT effectively resets the immune system by renewing the CD4 T cell compartment, especially the regulatory T cell population. The risk of transplant-related mortality (TRM) within the first 100 days should be weighed against the risk of disease-related mortality, and the careful selection and screening of patients before transplantation is essential. Systemic sclerosis is the first autoimmune disease for which HSCT has been shown, in a randomized, controlled trial, to be associated with increased TRM in the first year but a significant long-term, event-free survival benefit afterwards. In this Review, we discuss the immunological mechanisms of HSCT in various autoimmune diseases and current HSCT regimens. After carefully taking into consideration the risks and benefits of HSCT and alternative therapies, we also discuss the efficacy, complications and proposed indications of this procedure.

摘要

自体造血干细胞移植(HSCT)是唯一能够在几种难治性自身免疫性风湿病中诱导长期、无药物和无症状缓解的治疗方法。全世界已经进行了超过 3000 例用于治疗风湿和非风湿性严重自身免疫性疾病的 HSCT 手术。目前使用特定的预处理方案来消除患者的自身反应性免疫记忆。尽管许多方案中使用抗胸腺细胞球蛋白或抗-CD52 进行体内免疫细胞耗竭是常规做法,但从移植物中体外选择 CD34 干细胞存在争议。在与血清疗法和化疗相关的广泛免疫耗竭之后,HSCT 通过更新 CD4 T 细胞区室,特别是调节性 T 细胞群,有效地重置免疫系统。应权衡 100 天内移植相关死亡率(TRM)的风险与疾病相关死亡率的风险,并且在移植前对患者进行仔细的选择和筛选至关重要。系统性硬化症是第一个在随机对照试验中表明 HSCT 与第一年 TRM 增加相关但随后具有显著长期无事件生存获益的自身免疫性疾病。在这篇综述中,我们讨论了 HSCT 在各种自身免疫性疾病中的免疫学机制和当前的 HSCT 方案。在仔细考虑 HSCT 和替代疗法的风险和益处之后,我们还讨论了该程序的疗效、并发症和提出的适应证。

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