Division of Surgical Oncology, Department of Surgery, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
J Immunother. 2011 Jul-Aug;34(6):500-8. doi: 10.1097/CJI.0b013e318222ffc8.
We previously developed an antibody-avidin fusion protein (ch128.1Av) targeting the human transferrin receptor 1 (TfR1, also known as CD71), which demonstrates direct in vitro cytotoxicity against malignant hematopoietic cells. This cytotoxicity is attributed to its ability to decrease the level of TfR1 leading to lethal iron deprivation. We now report that ch128.1Av shows the ability to bind the Fcγ receptors and the complement component C1q, suggesting that it is capable of eliciting Fc-mediated effector functions such as antibody-dependent cell-mediated cytotoxicity and complement-mediated cytotoxicity. In addition, in 2 disseminated multiple myeloma xenograft mouse models, we show that a single dose of ch128.1Av results in significant antitumor activity, including long-term survival. It is interesting to note that the parental antibody without avidin (ch128.1) also shows remarkable in vivo anticancer activity despite its limited in vitro cytotoxicity. Finally, we demonstrate that ch128.1Av is not toxic to pluripotent hematopoietic progenitor cells using the long-term cell-initiating culture assay suggesting that these important progenitors would be preserved in different therapeutic approaches, including the in vitro purging of cancer cells for autologous transplantation and in vivo passive immunotherapy. Our results suggest that ch128.1Av and ch128.1 may be effective in the therapy of human multiple myeloma and potentially other hematopoietic malignancies.
我们之前开发了一种针对人转铁蛋白受体 1(TfR1,也称为 CD71)的抗体-抗生物素蛋白融合蛋白(ch128.1Av),该蛋白对恶性造血细胞具有直接的体外细胞毒性。这种细胞毒性归因于其降低 TfR1 水平导致致命铁剥夺的能力。我们现在报告 ch128.1Av 显示出结合 Fcγ 受体和补体成分 C1q 的能力,表明它能够引发 Fc 介导的效应功能,如抗体依赖性细胞介导的细胞毒性和补体介导的细胞毒性。此外,在 2 个弥散性多发性骨髓瘤异种移植小鼠模型中,我们表明单次给予 ch128.1Av 可导致显著的抗肿瘤活性,包括长期生存。有趣的是,尽管亲本抗体无抗生物素蛋白(ch128.1)在体外细胞毒性有限,但它也表现出显著的体内抗癌活性。最后,我们使用长期细胞起始培养测定法证明 ch128.1Av 对多能造血祖细胞没有毒性,这表明这些重要的祖细胞在不同的治疗方法中得到保留,包括用于自体移植的体外癌细胞清除和体内被动免疫疗法。我们的结果表明,ch128.1Av 和 ch128.1 可能对人类多发性骨髓瘤和潜在的其他造血恶性肿瘤的治疗有效。