Preston Robert Tisch Brain Tumor Center at Duke and Department of Pathology; Duke University Medical Center; Durham, NC USA.
MAbs. 2013 Sep-Oct;5(5):748-62. doi: 10.4161/mabs.25860. Epub 2013 Jul 25.
About 60 percent of glioblastomas highly express the gangliosides 3'-isoLM1 and 3',6'-isoLD1 on the cell surface, providing ideal targets for brain tumor immunotherapy. A novel recombinant immunotoxin, DmAb14m-(scFv)-PE38KDEL (DmAb14m-IT), specific for the gangliosides 3'-isoLM1 and 3',6'-isoLD1, was constructed with improved affinity and increased cytotoxicity for immunotherapeutic targeting of glioblastoma. We isolated an scFv parental clone from a previously established murine hybridoma, DmAb14, that is specific to both 3'-isoLM1 and 3',6'-isoLD1. We then performed in vitro affinity maturation by CDR hotspot random mutagenesis. The binding affinity and specificity of affinity-matured DmAb14m-IT were measured by surface-plasmon resonance, flow cytometry, and immunohistochemical analysis. In vitro cytotoxicity of DmAb14m-IT was measured by protein synthesis inhibition and cell death assays in human cell lines expressing gangliosides 3'-isoLM1 and 3',6'-isoLD1 (D54MG and D336MG) and xenograft-derived cells (D2224MG). As a result, the KD of DmAb14m-IT for gangliosides 3'-isoLM1 and 3',6'-isoLD1 was 2.6 × 10(-9)M. Also, DmAb14m-IT showed a significantly higher internalization rate in cells expressing 3'-isoLM1 and 3',6'-isoLD1. The DmAb14m-IT IC 50 was 80 ng/mL (1194 pM) on the D54MG cell line, 5 ng/ml (75 pM) on the D336MG cell line, and 0.5 ng/ml (7.5 pM) on the D2224MG xenograft-derived cells. There was no cytotoxicity on ganglioside-negative HEK293 cells. Immunohistochemical analysis confirmed the specific apparent affinity of DmAb14m-IT with 3'-isoLM1 and 3',6'-isoLD1. In conclusion, DmAb14m-IT showed specific binding affinity, a significantly high internalization rate, and selective cytotoxicity on glioma cell lines and xenograft-derived cells expressing 3'-isoLM1 and 3',6'-isoLD1, thereby displaying robust therapeutic potential for testing the antitumor efficacy of DmAb14m-IT at the preclinical level and eventually in the clinical setting.
约 60%的神经胶质瘤高度表达细胞表面的神经节苷脂 3'-isoLM1 和 3',6'-isoLD1,为脑肿瘤免疫治疗提供了理想的靶点。一种新型重组免疫毒素 DmAb14m-(scFv)-PE38KDEL(DmAb14m-IT)针对神经节苷脂 3'-isoLM1 和 3',6'-isoLD1 进行了构建,具有改善的亲和力和增加的细胞毒性,可用于免疫治疗神经胶质瘤。我们从先前建立的鼠杂交瘤 DmAb14 中分离出一个 scFv 亲本克隆,该克隆对 3'-isoLM1 和 3',6'-isoLD1 均具有特异性。然后,我们通过 CDR 热点随机诱变进行了体外亲和力成熟。通过表面等离子体共振、流式细胞术和免疫组织化学分析测量亲和力成熟的 DmAb14m-IT 的结合亲和力和特异性。通过蛋白质合成抑制和细胞死亡测定,在表达神经节苷脂 3'-isoLM1 和 3',6'-isoLD1 的人细胞系(D54MG 和 D336MG)和异种移植衍生细胞(D2224MG)中测量 DmAb14m-IT 的体外细胞毒性。结果,DmAb14m-IT 对神经节苷脂 3'-isoLM1 和 3',6'-isoLD1 的 KD 为 2.6×10(-9)M。此外,DmAb14m-IT 在表达 3'-isoLM1 和 3',6'-isoLD1 的细胞中显示出更高的内化率。DmAb14m-IT 在 D54MG 细胞系上的 IC50 为 80ng/ml(1194pM),在 D336MG 细胞系上为 5ng/ml(75pM),在 D2224MG 异种移植衍生细胞上为 0.5ng/ml(7.5pM)。在神经节苷脂阴性的 HEK293 细胞上没有细胞毒性。免疫组织化学分析证实了 DmAb14m-IT 与 3'-isoLM1 和 3',6'-isoLD1 的特异性明显亲和力。总之,DmAb14m-IT 对表达 3'-isoLM1 和 3',6'-isoLD1 的神经胶质瘤细胞系和异种移植衍生细胞显示出特异性结合亲和力、显著高的内化率和选择性细胞毒性,从而为在临床前水平和最终在临床环境中测试 DmAb14m-IT 的抗肿瘤疗效提供了强大的治疗潜力。