首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Direct and complement dependent cytotoxicity in CLL cells from patients with high-risk early-intermediate stage chronic lymphocytic leukemia (CLL) treated with alemtuzumab and rituximab.
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Direct and complement dependent cytotoxicity in CLL cells from patients with high-risk early-intermediate stage chronic lymphocytic leukemia (CLL) treated with alemtuzumab and rituximab.

机译:高危早期中中期慢性淋巴细胞性白血病(CLL)患者使用阿仑单抗和利妥昔单抗治疗后,CLL细胞的直接和补体依赖性细胞毒性。

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摘要

The mechanism of cytotoxicity of alemtuzumab and rituximab in chronic lymphocytic leukemia (CLL) is not well understood. We obtained fresh CLL cells from early-intermediate stage high-risk patients just prior to treatment with alemtuzumab and rituximab to study mechanisms of action and resistance. Alemtuzumab had minimal direct cytotoxicity but caused significant complement dependent cytotoxicity (CDC) although a subpopulation of CLL cells had intrinsic resistance. Rituximab had no direct cytotoxicity and caused minimal CDC in cells from most patients. These data suggest that CDC has a therapeutic role in patients treated with alemtuzumab and that measures to decrease resistance to CDC could increase efficacy.
机译:慢性淋巴细胞白血病(CLL)中阿仑单抗和利妥昔单抗的细胞毒性机制尚不清楚。我们在使用alemtuzumab和rituximab治疗之前从早期中高危患者中获得了新鲜的CLL细胞,以研究其作用和耐药机制。尽管CLL细胞亚群具有内在抗性,但Alemtuzumab的直接细胞毒性极小,但引起了明显的补体依赖性细胞毒性(CDC)。利妥昔单抗没有直接的细胞毒性,并且在大多数患者的细胞中仅引起最小的CDC。这些数据表明CDC在用alemtuzumab治疗的患者中具有治疗作用,并且降低CDC耐药性的措施可以提高疗效。

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