首页> 外文期刊>工程(英文) >Donor-Derived CD19-Targeted T Cell Infusion Eliminates B Cell Acute Lymphoblastic Leukemia Minimal Residual Disease with No Response to Donor Lymphocytes after Allogeneic Hematopoietic Stem Cell Transplantation
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Donor-Derived CD19-Targeted T Cell Infusion Eliminates B Cell Acute Lymphoblastic Leukemia Minimal Residual Disease with No Response to Donor Lymphocytes after Allogeneic Hematopoietic Stem Cell Transplantation

机译:供体来源的CD19靶向T细胞输注消除了异基因造血干细胞移植后对供体淋巴细胞无反应的B细胞急性淋巴细胞白血病的最小残留疾病。

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摘要

Leukemia relapse is still the leading cause of treatment failure after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for B cell acute lymphoblastic leukemia (B-ALL).Relapsed patients with BALL after allo-HSCT have a very short median survival.Minimal residual disease (MRD) is predictive of forthcoming hematological relapse after hematopoietic stem cell transplantation (HSCT);furthermore,eliminating MRD effectively prevents relapse.Donor lymphoblastic infusion (DLI) is the main established approach to treat B-ALL with MRD after allo-HSCT.However,about one-third of patients with MRD are non-responsive to DLI and their prognosis worsens.Although donor-derived cluster of differentiation (CD)19-directed chimeric antigen receptor-modified (CAR) T cells (CART19s) can potentially cure leukemia,the efficiency and safety of infusions with these cells have not yet been investigated in patients with MRD after HSCT.Between September 2014 and February 2018,six patients each received one or more infusions of CART19s from HSCT donors.Five (83.33%) achieved MRD-negative remission,and one case was not responsive to the administration of CAR T cells.Three of the six patients are currently alive without leukemia.No patient developed acute graft-versus-host disease (aGVHD),and no patient died of cytokine release syndrome.Donor-derived CAR T cell infusions seem to be an effective and safe intervention for patients with MRD in B-ALL after allo-HSCT and for those who were not responsive to DLI.
机译:白血病复发仍然是异基因造血干细胞移植(allo-HSCT)后B细胞急性淋巴细胞白血病(B-ALL)治疗失败的主要原因。异基因-HSCT术后复发的BALL患者中位生存期非常短,残留量最小疾病(MRD)可以预测造血干细胞移植(HSCT)后即将发生的血液学复发;此外,消除MRD可以有效地预防复发。然而,约有三分之一的MRD患者对DLI无反应,并且预后恶化。尽管供体来源的分化簇(CD)19定向嵌合抗原受体修饰(CAR)T细胞(CART19s)可以治愈白血病,HSCT后MRD患者输注这些细胞的效率和安全性尚未得到研究。2014年9月至2018年2月,每例接受了6名患者一次或多次从HSCT供体中注入CART19s。5例(83.33%)实现了MRD阴性缓解,其中1例对CAR T细胞的给药没有反应。6例患者中有3例没有白血病存活,没有患者出现急性移植物抗宿主病(aGVHD),无一例死于细胞因子释放综合征。对于异基因造血干细胞移植术后B-ALL的MRD患者和那些对DLI没有反应。

著录项

  • 来源
    《工程(英文)》 |2019年第001期|150-155|共6页
  • 作者单位

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Shenzhen Geno-Immune Medical Institute, Shenzhen 518057, China;

    Innovative Cellular Therapeutics Co., Ltd., Shanghai 201499, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

    Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University Institute of Hematology,Peking University People's Hospital,Beijing 100044, China;

    Collaborative Innovation Center of Hematology, Peking University, Beijing 100084, China;

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