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Autologous Nonmyeloablative Hematopoietic Stem Cell Transplantation in New-Onset Type 1 Diabetes: A Multicenter Analysis

机译:新发1型糖尿病的自体非清髓性造血干细胞移植:多中心分析

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摘要

Type 1 diabetes (T1D) is one of the major autoimmune diseases affecting children and young adults worldwide. To date, the different immunotherapies tested have achieved insulin independence in <5% of treated individuals. Recently, a novel hematopoietic stem cell (HSC)-based strategy has been tested in individuals with new-onset T1D. The aim of this study was to determine the effects of autologous nonmyeloablative HSC transplantation in 65 individuals with new-onset T1D who were enrolled in two Chinese centers and one Polish center, pooled, and followed up for 48 months. A total of 59% of individuals with T1D achieved insulin independence within the first 6 months after receiving conditioning immunosuppression therapy (with antithy-mocyte globulin and cyclophosphamide) and a single infusion of autologous HSCs, and 32% remained insulin independent at the last time point of their follow-up. All treated subjects showed a decrease in HbA_(1c) levels and an increase in C-peptide levels compared with pretreat-ment. Despite a complete immune system recovery (i.e., leukocyte count) after treatment, 52% of treated individuals experienced adverse effects. Our study suggests the following: 1) that remission of T1D is possible by combining HSC transplantation and immunosuppression; 2) that autologous nonmyeloablative HSC transplantation represents an effective treatment for selected individuals with T1D; and 3) that safer HSC-based therapeutic options are required.
机译:1型糖尿病(T1D)是影响全球儿童和年轻人的主要自身免疫疾病之一。迄今为止,所测试的不同免疫疗法已在<5%的治疗个体中实现了胰岛素独立性。最近,一种新的基于造血干细胞(HSC)的策略已在新发T1D患者中进行了测试。这项研究的目的是确定65例新发T1D患者的自体非清髓性HSC移植的效果,这些患者被纳入了两个中国中心和一个波兰中心,汇总并随访48个月。共有59%的T1D患者在接受条件免疫抑制治疗(使用抗胸腺细胞球蛋白和环磷酰胺)并单次输注自体HSC后的前6个月内获得了胰岛素独立性,在最后一个时间点仍保持胰岛素独立性为32%他们的后续行动。与治疗前相比,所有接受治疗的受试者均表现出HbA_(1c)水平降低和C肽水平升高。尽管治疗后免疫系统完全恢复(即白细胞计数),但仍有52%的受治疗者出现了不良反应。我们的研究提出以下几点:1)通过结合HSC移植和免疫抑制可以缓解T1D。 2)自体非清髓性HSC移植代表了某些T1D个体的有效治疗方法; 3)需要更安全的基于HSC的治疗选择。

著录项

  • 来源
    《Diabetes》 |2014年第9期|3041-3046|共6页
  • 作者单位

    Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA,Transplant Medicine, IRCCS San Raffaele Hospital, Milan, Italy;

    Transplant Medicine, IRCCS San Raffaele Hospital, Milan, Italy;

    Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA;

    Department of Internal Diseases, Diabetology and Endocrinology, Central Hospital, Ministry of Interior Affairs and Administration, Warsaw, Poland,Department of Endocrinology, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland;

    Division of Endocrinology, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, Jiangsu, People's Republic of China;

    Division of Endocrinology, The Affiliated Drum Tower Hospital of Nanjing University, Nanjing, Jiangsu, People's Republic of China;

    Shangai Jiao Tong University School of Medicine, Shanghai, People's Republic of China;

    Department of Hematology, Oncology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland;

    Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA,Transplant Medicine, IRCCS San Raffaele Hospital, Milan, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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