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A single-domain antibody-linked Fab bispecific antibody Her2-S-Fab has potent cytotoxicity against Her2-expressing tumor cells

机译:单域抗体连接的Fab双特异性抗体Her2-S-Fab对表达Her2的肿瘤细胞具有强大的细胞毒性

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摘要

Her2, which is frequently overexpressed in breast cancer, is one of the most studied tumor-associated antigens for cancer therapy. Anti-HER2 monoclonal antibody, trastuzumab, has achieved significant clinical benefits in metastatic breast cancer. In this study, we describe a novel bispecific antibody Her2-S-Fab targeting Her2 by linking a single domain anti-CD16 VHH to the trastuzumab Fab. The Her2-S-Fab antibody can be efficiently expressed and purified from Escherichia coli, and drive potent cancer cell killing in HER2-overexpressing cancer cells. In xenograft model, the Her2-S-Fab suppresses tumor growth in the presence of human immune cells. Our results suggest that the bispecific Her2-S-Fab may provide a valid alternative to Her2 positive cancer therapy.
机译:Her2在乳腺癌中经常过度表达,是癌症研究中研究最多的肿瘤相关抗原之一。抗HER2单克隆抗体曲妥珠单抗在转移性乳腺癌中取得了显着的临床益处。在这项研究中,我们通过将单域抗CD16 VHH连接至曲妥珠单抗Fab描述了靶向Her2的新型双特异性抗体Her2-S-Fab。 Her2-S-Fab抗体可从大肠杆菌中高效表达和纯化,并在过表达HER2的癌细胞中驱动有效的癌细胞杀伤作用。在异种移植模型中,Her2-S-Fab在人类免疫细胞的存在下抑制肿瘤的生长。我们的结果表明,双特异性Her2-S-Fab可以为Her2阳性癌症治疗提供有效的替代方法。

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