Parakh Sagun, Huynh Nhi, Cao Diana Dong, Rigopoulos Angela, Gloria Benjamin, Burvenich Ingrid J G, Murone Carmel, Wichmann Christian W, Guo Nancy Yanan, Senko Clare, Parslow Adam, Allan Laura, Osellame Laura D, Janes Peter W, Scott Fiona E, Liu Zhanqi, Gan Hui K, Scott Andrew M
Tumour Targeting Laboratory, Olivia Newton-John Cancer Research Institute, Melbourne, Australia.
Department of Medical Oncology, Austin Health, Melbourne, Australia.
Mol Cancer Ther. 2025 Sep 2;24(9):1442-1452. doi: 10.1158/1535-7163.MCT-24-0583.
We generated a novel HER2 mAb104, which binds to an epitope in domain II of HER2 that is conformationally exposed in tumors in response to HER2 amplification or activation but is not accessible to antibody binding in normal tissues. Consistent with other studies that evaluated antibodies targeting conformationally exposed epitopes, mAb104 lacked in vitro activity but showed potent antitumor activity in vivo. The antitumor effect in vivo was similar in magnitude to trastuzumab and pertuzumab, and combination with trastuzumab was superior to trastuzumab alone. IHC screening of normal and tumor tissues with mAb104 showed that mAb104 did not bind to normal tissues, confirming the tumor specificity of mAb104. In vivo biodistribution and imaging data demonstrated specific tumor targeting of mAb104 in HER2-expressing tumors. Confocal microscopy clearly demonstrated the internalization of mAb104 into the tumor cells, consistent with mAb104:HER2 trafficking. mAb104 is tumor-specific, exhibits potent antitumor activity in HER2-positive models, and internalizes into HER2-positive tumor cells. These results demonstrate the potential of mAb104 as a novel HER2-targeting therapy, both as a naked antibody for signaling abrogation therapy and for payload delivery as an antibody-drug conjugate or for β/α particle therapy.
我们制备了一种新型HER2单克隆抗体mAb104,它与HER2结构域II中的一个表位结合,该表位在肿瘤中因HER2扩增或激活而呈构象暴露,但在正常组织中抗体无法结合。与其他评估靶向构象暴露表位抗体的研究一致,mAb104缺乏体外活性,但在体内显示出强大的抗肿瘤活性。体内抗肿瘤效果在程度上与曲妥珠单抗和帕妥珠单抗相似,并且与曲妥珠单抗联合使用优于单独使用曲妥珠单抗。用mAb104对正常组织和肿瘤组织进行免疫组化筛查表明,mAb104不与正常组织结合,证实了mAb104的肿瘤特异性。体内生物分布和成像数据表明mAb104在表达HER2的肿瘤中具有特异性肿瘤靶向性。共聚焦显微镜清楚地证明了mAb104内化到肿瘤细胞中,这与mAb104:HER2的转运一致。mAb104具有肿瘤特异性,在HER2阳性模型中表现出强大的抗肿瘤活性,并内化到HER2阳性肿瘤细胞中。这些结果证明了mAb104作为一种新型HER2靶向治疗药物的潜力,既可以作为裸抗体用于信号消除治疗,也可以作为抗体-药物偶联物用于递送有效载荷或用于β/α粒子治疗。