首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Defucosylated humanized anti-CCR4 monoclonal antibody KW-0761 as a novel immunotherapeutic agent for adult T-cell leukemia/lymphoma.
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Defucosylated humanized anti-CCR4 monoclonal antibody KW-0761 as a novel immunotherapeutic agent for adult T-cell leukemia/lymphoma.

机译:去岩藻糖基化的人源化抗CCR4单克隆抗体KW-0761,作为成人T细胞白血病/淋巴瘤的新型免疫治疗剂。

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PURPOSE: Adult T-cell leukemia/lymphoma (ATLL) has a very poor prognosis. We have developed the humanized defucosylated anti-CC chemokine receptor 4 (CCR4) monoclonal antibody KW-0761 as a next generation immunotherapeutic agent. The first aim of the present study was to evaluate whether the antitumor activity of KW-0761 would likely be sufficient for therapeutic clinical application against ATLL. The second aim was to fully elucidate the mechanism of antibody-dependent cellular cytotoxicity (ADCC) mediated by this defucosylated monoclonal antibody. EXPERIMENTAL DESIGN: The antitumor activity of KW-0761 against ATLL cell lines was evaluated in vitro using human cells and in mice in vivo. Primary ATLL cells from 23 patients were evaluated for susceptibility to autologous ADCC with KW-0761 by two independent methods. RESULTS: KW-0761 showed potent antitumor activity against ATLL cell lines both in vitro and in the ATLL mouse model in vivo. In addition, KW-0761 showed potent antitumor activity mediated by highly enhanced ADCC against primary ATLL cells both in vitro and ex vivo in an autologous setting. The degree of KW-0761 ADCC against primary ATLL cells in an autologous setting was mainly determined by the amount of effector natural killer cells present, but not the amount of the target molecule CCR4 on the ATLL cell surface. CONCLUSION: KW-0761 should be sufficiently active for therapeutic clinical application for ATLL. In addition, combination treatment strategies that augment natural killer cell activity should be promising for amplifying the effect of KW-0761. In the near future, the actual efficacy of KW-0761 will be established in pivotal clinical trials.
机译:目的:成人T细胞白血病/淋巴瘤(ATLL)的预后很差。我们已经开发了人源化的去岩藻糖基化抗CC趋化因子受体4(CCR4)单克隆抗体KW-0761作为下一代免疫治疗剂。本研究的第一个目的是评估KW-0761的抗肿瘤活性是否可能足以针对ATLL进行治疗性临床应用。第二个目的是充分阐明这种去岩藻糖基化的单克隆抗体介导的抗体依赖性细胞毒作用(ADCC)的机制。实验设计:在体外使用人细胞和在体内小鼠中评估了KW-0761对ATLL细胞系的抗肿瘤活性。通过两种独立的方法,评估了来自23位患者的原代ATLL细胞对KW-0761对自体ADCC的敏感性。结果:KW-0761在体外和ATLL小鼠模型中均显示出对ATLL细胞系的有效抗肿瘤活性。另外,KW-0761在体外和离体在自体环境中均显示出由高度增强的ADCC介导的针对原代ATLL细胞的有效抗肿瘤活性。在自体环境中,KW-0761 ADCC针对原代ATLL细胞的程度主要取决于存在的效应子自然杀伤细胞的数量,而不取决于ATLL细胞表面上靶分子CCR4的数量。结论:KW-0761应具有足够的活性,可用于ATLL的治疗性临床应用。此外,增强自然杀伤细胞活性的联合治疗策略应有望扩大KW-0761的作用。在不久的将来,将在关键的临床试验中确定KW-0761的实际功效。

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