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去岩藻糖化人源化抗 CCR4 单克隆抗体 KW-0761 作为一种新型免疫治疗剂用于治疗成人 T 细胞白血病/淋巴瘤。

Defucosylated humanized anti-CCR4 monoclonal antibody KW-0761 as a novel immunotherapeutic agent for adult T-cell leukemia/lymphoma.

机构信息

Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.

出版信息

Clin Cancer Res. 2010 Mar 1;16(5):1520-31. doi: 10.1158/1078-0432.CCR-09-2697. Epub 2010 Feb 16.

Abstract

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.

摘要

目的

成人 T 细胞白血病/淋巴瘤(ATLL)预后极差。我们开发了人源化去岩藻糖基化抗 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药物。本研究的首要目的是评估 KW-0761 的抗肿瘤活性是否足以用于治疗 ATLL。第二个目的是充分阐明该去岩藻糖基化单克隆抗体介导的抗体依赖性细胞毒性(ADCC)的机制。

实验设计

体外用人细胞和体内小鼠模型评估 KW-0761 对 ATLL 细胞系的抗肿瘤活性。通过两种独立的方法评估 23 例患者的原发性 ATLL 细胞对 KW-0761 的自体 ADCC 敏感性。

结果

KW-0761 对 ATLL 细胞系在体外和体内 ATLL 小鼠模型中均显示出强大的抗肿瘤活性。此外,KW-0761 在体外和自体环境下的离体试验中,通过高度增强的 ADCC 对原发性 ATLL 细胞显示出强大的抗肿瘤活性。在自体环境下 KW-0761 对原发性 ATLL 细胞的 ADCC 程度主要取决于存在的效应自然杀伤细胞的数量,而不是 ATLL 细胞表面 CCR4 靶分子的数量。

结论

KW-0761 对 ATLL 的治疗临床应用应具有足够的活性。此外,增强自然杀伤细胞活性的联合治疗策略有望增强 KW-0761 的效果。在不久的将来,将在关键性临床试验中确定 KW-0761 的实际疗效。

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