Glycotope GmbH, Robert-Roessle-Str.10, 13125 Berlin, Germany.
Karyon Biopharma Consulting e.U., Brunn am Gebirge, Austria.
Int J Mol Sci. 2024 Jan 24;25(3):1406. doi: 10.3390/ijms25031406.
GT-00AxIL15 is a novel interleukin-15-based immunocytokine targeting a tumor-specific, glycosylated epitope of MUC1 (TA-MUC1). We characterized mode of action, pharmacokinetic (PK) and pharmacodynamic (PD) properties and investigated the relevance of TA-MUC1 binding for the concept of delivering IL-15 to solid tumors. In vitro pharmacology was analyzed in binding and cell-based assays. The in vivo PK profile and IL-15-mediated PD effects of GT-00AxIL15 were investigated in tumor-free mice. Tumor accumulation, immune infiltration and anti-tumor activity were assessed in TA-MUC1+ syngeneic and xenogeneic murine tumor models. GT-00AxIL15 was shown to specifically bind TA-MUC1 on tumor cells via its mAb moiety, to IL-15 receptors on immune cells via its IL-15 fusion modules and to FcγRs via its functional Fc-part. In vitro, NK, NKT and CD8+ T cells were activated and proliferated, leading to anti-tumor cytotoxicity and synergism with antibody-dependent cellular cytotoxicity (ADCC)-mediating mAbs. In vivo, GT-00AxIL15 exhibited favorable PK characteristics with a serum half-life of 13 days and specifically accumulated in TA-MUC1+ tumors. In the tumor microenvironment, GT-00AxIL15 induced robust immune activation and expansion and mediated anti-metastatic and anti-tumor effects in syngeneic and xenograft tumor models. These results support the rationale to improve PK and anti-tumor efficacy of IL-15 by increasing local concentrations at the tumor site via conjugation to a TA-MUC1 binding mAb. The tumor-selective expression pattern of TA-MUC1, powerful immune activation and anti-tumor cytotoxicity, long serum half-life and tumor targeting properties, render GT-00AxIL15 a promising candidate for treatment of solid tumors with high medical need, e.g., ovarian, lung and breast cancer.
GT-00AxIL15 是一种新型白细胞介素-15 免疫细胞因子,针对 MUC1 的肿瘤特异性糖基化表位(TA-MUC1)。我们对其作用模式、药代动力学(PK)和药效动力学(PD)特性进行了表征,并研究了 TA-MUC1 结合对于将白细胞介素-15 递送至实体瘤的概念的相关性。在结合和基于细胞的测定中分析了体外药理学。在无肿瘤小鼠中研究了 GT-00AxIL15 的体内 PK 特征和 IL-15 介导的 PD 效应。在 TA-MUC1+同源和异种小鼠肿瘤模型中评估了肿瘤蓄积、免疫浸润和抗肿瘤活性。研究表明,GT-00AxIL15 通过其 mAb 部分特异性结合肿瘤细胞上的 TA-MUC1,通过其白细胞介素-15 融合模块结合免疫细胞上的白细胞介素-15 受体,通过其功能 Fc 部分结合 FcγRs。体外,NK、NKT 和 CD8+T 细胞被激活和增殖,导致抗肿瘤细胞毒性,并与抗体依赖性细胞毒性(ADCC)介导的 mAb 产生协同作用。体内,GT-00AxIL15 表现出良好的 PK 特征,血清半衰期为 13 天,特异性积聚在 TA-MUC1+肿瘤中。在肿瘤微环境中,GT-00AxIL15 诱导强烈的免疫激活和扩增,并在同源和异种移植肿瘤模型中介导抗转移和抗肿瘤作用。这些结果支持通过与结合 TA-MUC1 的 mAb 缀合来增加肿瘤部位的局部浓度以提高白细胞介素-15 的 PK 和抗肿瘤疗效的原理。TA-MUC1 的肿瘤选择性表达模式、强大的免疫激活和抗肿瘤细胞毒性、长血清半衰期和肿瘤靶向特性,使 GT-00AxIL15 成为治疗高医疗需求实体瘤的有前途的候选药物,例如卵巢癌、肺癌和乳腺癌。