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TIM-3 as a therapeutic target for malignant stem cells in acute myelogenous leukemia

机译:TIM-3作为急性髓性白血病中恶性干细胞的治疗靶标

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Acute myeloid leukemia (AML) originates from self-renewing leukemic stem cells (LSCs), an ultimate therapeutic target for AML. Recent studies have shown that many AML LSC-specific surface antigens could be such candidates. T cell immunoglobulin mucin-3 (TIM-3) is expressed on LSCs in most types of AML, except for acute promyelocytic leukemia, but not on normal hematopoietic stem cells (HSCs). In mouse models reconstituted with human AML LSCs or human hematopoietic stem cells, a human TIM-3 mouse IgG2a antibody with complement-dependent and antibody-dependent cellular cytotoxic activities eradicates AML LSCs in vivo but does not affect normal human hematopoiesis. Thus, TIM-3 is one of the promising targets to eradicate AML LSCs.
机译:急性髓性白血病(AML)起源于自我更新的白血病干细胞(LSCs),是AML的最终治疗靶标。最近的研究表明,许多AML LSC特异性表面抗原可能是这样的候选者。除急性早幼粒细胞白血病外,急性早幼细胞白血病除了正常造血干细胞(HSCs)外,T细胞免疫球蛋白粘蛋白-3(TIM-3)在大多数类型的AML中表达。在用人AML LSCs或人造血干细胞重构的小鼠模型中,具有补体依赖性和抗体依赖性细胞细胞毒性活性的人TIM-3小鼠IgG2A抗体在体内灭绝了AML LSC但不影响正常的人血液血液。因此,Tim-3是用于消除AML LSCs的有希望的目标之一。

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