Acute lymphoblastic leukemia cells that survive combination chemotherapy in vivo remain sensitive to allogeneic immune effects

被引:7
|
作者
Jansson, Johan [1 ,3 ]
Hsu, Yu-Chiao [1 ]
Kuzin, Igor I. [2 ]
Campbell, Andrew [1 ]
Mullen, Craig A. [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Pediat, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Med, Rochester, NY 14642 USA
[3] Univ Kalmar, Sch Pure & Appl Nat Sci, Kalmar, Sweden
基金
美国国家卫生研究院;
关键词
Graft versus leukemia effect; Allogeneic hematopoietic stem cell transplantation; Acute lymphoblastic leukemia; Chemotherapy; Cancer immunology; Graft versus host disease; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; CELLULAR-DRUG RESISTANCE; BLOOD NATURAL-KILLER; PROGNOSTIC-SIGNIFICANCE; TUMOR-ACTIVITY; B-CELL; CHILDHOOD; GRAFT; LYMPHOCYTES;
D O I
10.1016/j.leukres.2010.10.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Allogeneic hematopoietic stem cell transplantation is often performed for patients with acute lymphoblastic leukemia (ALL) whose disease has relapsed after chemotherapy treatment. However, graft versus leukemia (GVL) effects in ALL are generally weak and the mechanisms of this weakness are unknown. These studies tested the hypothesis that ALL cells that have survived conventional chemotherapy in vivo acquire relative resistance to the allogeneic GVL effect. C57BL/6 mice were injected with murine pre-B ALL lines driven by human mutations and then were treated with combination chemotherapy. ALL cells surviving therapy were analysed in vitro and in vivo for acquisition of resistance to chemotherapy, radiation, cytolytic T cells, NK cells, LAK cells and cytokines. In vivo drug treatment did lead to leukemia population with more rapid proliferation and also decreased sensitivity to vincristine, doxorubicin and radiation. However, drug treatment did not produce ALL populations that were less sensitive to GVL effects in vitro or in vivo. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:800 / 807
页数:8
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