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Defucosylated Humanized Anti-CCR4 Monoclonal Antibody KW-0761 as a Novel Immunotherapeutic Agent for Adult T-cell Leukemia/Lymphoma

抗体依赖性细胞介导的细胞毒性 单克隆抗体 白血病 癌症研究 体内 中央控制室4 免疫学 医学 淋巴瘤 抗体 药理学 生物 免疫系统 趋化因子 趋化因子受体 生物技术
作者
Toshihiko Ishii,Takashi Ishida,Atae Utsunomiya,Atsushi Inagaki,Hiroki Yano,Hirokazu Komatsu,Shinsuke Iida,Kazunori Imada,Takashi Uchiyama,Shiro Akinaga,Kenya Shitara,Ryuzo Ueda
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:16 (5): 1520-1531 被引量:205
标识
DOI:10.1158/1078-0432.ccr-09-2697
摘要

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.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.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.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.

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