自体造血干细胞移植治疗多发性硬化症的高剂量免疫抑制疗法:目前的观点

Q4 Medicine
A. Polushin, E. Lopatina, Yury R. Zalyalov, A. Tsynchenko, N. Totolyan, A. Kulagin
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引用次数: 1

摘要

自体造血干细胞移植(aHSCT)后高剂量免疫抑制治疗是治疗自身免疫性疾病(包括多发性硬化症(MS))的一种有希望和有效的方法。在过去的15-20年里,aHSCT不良事件的频率和严重程度在调节方案强度降低后有所下降。更好地了解免疫重建的免疫学机制和更好地选择患者进行该手术的方法也导致了改善的结果。鉴于世界范围内多发性硬化症发病率的增加,以及标准治疗的有效性不足,将自体移植纳入多发性硬化症治疗的临床指南可以维持劳动力人群的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-dose immunosuppressive therapy with autologous hematopoietic stem cells transplantation for multiple sclerosis: Current view
Autologous hematopoietic stem cells transplantation (aHSCT) followed by high-dose immunosuppressive therapy is a promising and effective method of treating autoimmune diseases, including multiple sclerosis (MS). Over the past 15-20 years, frequency and severity of adverse events in aHSCT were decreased after reducing the intensity of conditioning regimens. Both better understanding of the immunological mechanisms of immune reconstitution and better approach to the selection of patients for this procedure also led to improved results. In view of increased incidence of multiple sclerosis worldwide, as well as insufficient effectiveness of standard therapy, the introduction of autologous transplantation into clinical guidelines for the MS treatment could maintain quality of life in the workforce population.
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来源期刊
Cellular Therapy and Transplantation
Cellular Therapy and Transplantation Medicine-Transplantation
CiteScore
0.60
自引率
0.00%
发文量
31
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