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体内经联合化疗存活的急性淋巴细胞白血病细胞仍然对同种异体免疫效应敏感。

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

机构信息

Department of Pediatrics, University of Rochester, Medical Center, Rochester, NY 14642, USA.

出版信息

Leuk Res. 2011 Jun;35(6):800-7. doi: 10.1016/j.leukres.2010.10.018. Epub 2010 Nov 12.

Abstract

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.

摘要

同种异体造血干细胞移植常用于治疗化疗后复发的急性淋巴细胞白血病(ALL)患者。然而,ALL 中的移植物抗白血病(GVL)效应通常较弱,其机制尚不清楚。这些研究检验了以下假设,即体内经常规化疗存活的 ALL 细胞获得了对同种异体 GVL 效应的相对抗性。C57BL/6 小鼠被注射了由人类突变驱动的鼠前 B 淋巴细胞白血病系,然后接受联合化疗。在体外和体内分析了对化疗、辐射、细胞毒性 T 细胞、NK 细胞、LAK 细胞和细胞因子具有抗性的 ALL 细胞。体内药物治疗确实导致白血病群体具有更快的增殖速度,并且对长春新碱、阿霉素和辐射的敏感性降低。然而,药物治疗并未产生对体外或体内 GVL 效应的敏感性降低的 ALL 群体。

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