INSERM U976, Hôpital Saint Louis, Paris, France. University Paris Diderot, Sorbonne Paris Cité, UMRS 976, Paris, France.
INNATE PHARMA, Marseilles, France.
Cancer Res. 2014 Nov 1;74(21):6060-70. doi: 10.1158/0008-5472.CAN-14-1456.
Advanced cutaneous T-cell lymphoma (CTCL) remains an unmet medical need, which lacks effective targeted therapies. In this study, we report the development of IPH4102, a humanized monoclonal antibody that targets the immune receptor KIR3DL2, which is widely expressed on CTCL cells but few normal immune cells. Potent antitumor properties of IPH4102 were documented in allogeneic human CTCL cells and a mouse model of KIR3DL2(+) disease. IPH4102 antitumor activity was mediated by antibody-dependent cell cytotoxicity and phagocytosis. IPH4102 improved survival and reduced tumor growth in mice inoculated with KIR3DL2(+) tumors. Ex vivo efficacy was further evaluated in primary Sézary patient cells, sorted natural killer-based autologous assays, and direct spiking into Sézary patient peripheral blood mononuclear cells. In these settings, IPH4102 selectively and efficiently killed primary Sézary cells, including at unfavorable effector-to-target ratios characteristic of unsorted PBMC. Together, our results offer preclinical proof of concept for the clinical development of IPH4102 to treat patients with advanced CTCL.
晚期皮肤 T 细胞淋巴瘤(CTCL)仍然是一个未满足的医学需求,缺乏有效的靶向治疗方法。在这项研究中,我们报告了 IPH4102 的开发,这是一种针对免疫受体 KIR3DL2 的人源化单克隆抗体,该受体广泛表达于 CTCL 细胞,但在少数正常免疫细胞上表达。在同种异体人 CTCL 细胞和 KIR3DL2(+)疾病的小鼠模型中,证明了 IPH4102 具有强大的抗肿瘤特性。IPH4102 的抗肿瘤活性是通过抗体依赖性细胞细胞毒性和吞噬作用介导的。在接种 KIR3DL2(+)肿瘤的小鼠中,IPH4102 提高了存活率并减少了肿瘤生长。在原发性 Sézary 患者细胞、基于自然杀伤细胞的自体检测和直接掺入 Sézary 患者外周血单核细胞的体外功效中进一步进行了评估。在这些情况下,IPH4102 选择性且有效地杀死了原发性 Sézary 细胞,包括在未分选的 PBMC 中特征性的不利的效应物与靶标比值。综上所述,我们的结果提供了 IPH4102 用于治疗晚期 CTCL 患者的临床开发的临床前概念验证。