Department of Biomedical Engineering, The Ohio State University (OSU), 151 West Woodruff Ave, Columbus, OH 43210, USA.
Department of Chemical and Biomolecular Engineering, The Ohio State University (OSU), 151 W Woodruff Ave, Columbus, OH 43210, USA.
Cells. 2023 Sep 30;12(19):2393. doi: 10.3390/cells12192393.
Non-small cell lung cancer (NSCLC) patients, accounting for approximately 85% of lung cancer cases, are usually diagnosed in advanced stages. Traditional surgical resection and radiotherapy have very limited clinical benefits. The objective of this study was to develop and evaluate a targeted therapy, antibody-drug conjugate (ADC), for NSCLC treatment. Specifically, the CD276 receptor was evaluated and confirmed as an ideal surface target of NSCLC in the immunohistochemistry (IHC) staining of seventy-three patient tumor microarrays and western blotting analysis of eight cell lines. Our anti-CD276 monoclonal antibody (mAb) with cross-activity to both human and mouse receptors showed high surface binding, effective drug delivery and tumor-specific targeting in flow cytometry, confocal microscopy, and in vivo imaging system analysis. The ADC constructed with our CD276 mAb and payload monomethyl auristatin F (MMAF) showed high anti-NSCLC cytotoxicity to multiple lines and effective anti-tumor efficacy in both immunocompromised and immunocompetent NSCLC xenograft mouse models. The brief mechanism study revealed the integration of cell proliferation inhibition and immune cell reactivation in tumor microenvironments. The toxicity study did not detect off-target immune toxicity or peripheral toxicity. Altogether, this study suggested that anti-CD276 ADC could be a promising candidate for NSCLC treatment.
非小细胞肺癌(NSCLC)患者约占肺癌病例的 85%,通常在晚期诊断。传统的手术切除和放疗的临床获益非常有限。本研究旨在开发和评估一种针对 NSCLC 的靶向治疗药物,抗体药物偶联物(ADC)。具体来说,通过对 73 例患者肿瘤微阵列的免疫组织化学(IHC)染色和 8 个细胞系的 Western blot 分析,评估并证实 CD276 受体是 NSCLC 的理想表面靶标。我们的抗 CD276 单克隆抗体(mAb)对人和鼠受体均具有交叉活性,在流式细胞术、共聚焦显微镜和体内成像系统分析中显示出高表面结合、有效药物传递和肿瘤特异性靶向性。我们构建的抗 CD276 mAb 和载药单甲基澳瑞他汀 F(MMAF)的 ADC 对多种细胞系具有高抗 NSCLC 细胞毒性,并在免疫缺陷和免疫功能正常的 NSCLC 异种移植小鼠模型中显示出有效的抗肿瘤疗效。简要的机制研究揭示了细胞增殖抑制和肿瘤微环境中免疫细胞再激活的整合。毒性研究未检测到脱靶免疫毒性或外周毒性。总之,这项研究表明,抗 CD276 ADC 可能是治疗 NSCLC 的一种有前途的候选药物。