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Targeting chronic lymphocytic leukemia cells with a humanized monoclonal antibody specific for CD44

机译:用对CD44特异的人源化单克隆抗体靶向慢性淋巴细胞白血病

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摘要

Chronic lymphocytic leukemia (CLL) cells express high levels of CD44, a cell-surface glycoprotein receptor for hyaluronic acid. We found that a humanized mAb specific for CD44 (RG7356) was directly cytotoxic for leukemia B cells, but had little effect on normal B cells. Moreover, RG7356 could induce CLL cells that expressed the zeta-associated protein of 70 kDa (ZAP-70) to undergo caspase-dependent apoptosis, independent of complement or cytotoxic effector cells. The cytotoxic effect of this mAb was not mitigated when the CLL cells were cocultured with mesenchymal stromal cells (MSCs) or hyaluronic acid or when they were stimulated via ligation of the B-cell receptor with anti-µ. RG7356 induced rapid internalization of CD44 on CLL cells at 37 °C, resulting in reduced expression of ZAP-70, which we found was complexed with CD44. Administration of this mAb at a concentration of 1 mg/kg to immune-deficient mice engrafted with human CLL cells resulted in complete clearance of engrafted leukemia cells. These studies indicate that this mAb might have therapeutic activity, particularly in patients with CLL that express ZAP-70.
机译:慢性淋巴细胞性白血病(CLL)细胞表达高水平的CD44,一种透明质酸的细胞表面糖蛋白受体。我们发现,特异性针对CD44的人源化单克隆抗体(RG7356)对白血病B细胞具有直接的细胞毒性,但对正常B细胞​​的影响很小。此外,RG7356可以诱导表达70 kDa的Zeta相关蛋白(ZAP-70)的CLL细胞经历caspase依赖性凋亡,而不受补体或细胞毒性效应细胞的影响。当CLL细胞与间充质基质细胞(MSC)或透明质酸共培养时,或通过B细胞受体与抗µ的连接刺激时,该mAb的细胞毒性作用并未减弱。 RG7356在37°C诱导CLL细胞上CD44迅速内在化,导致ZAP-70表达降低,我们发现它与CD44形成复合物。以1 mg / kg的浓度向植入人CLL细胞的免疫缺陷小鼠施用此mAb可以完全清除植入的白血病细胞。这些研究表明,该mAb可能具有治疗活性,特别是对于表达ZAP-70的CLL患者。

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