Xing Jieyu, Lin Limin, Li Jing, Liu Jiayu, Zhou Changhua, Pan Haitao, Shu Rui, Dong Bin, Cao Donglin, Li Qing, Wang Zhong
School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, China 510006; Center for Cellular & Structural Biology, Sun Yat-Sen University, Guangzhou, China 510006.
Ying Rui Inc., Guangzhou, Guangdong, China 510009.
Transl Oncol. 2017 Oct;10(5):780-785. doi: 10.1016/j.tranon.2017.07.003. Epub 2017 Aug 7.
Among different cancer immunotherapy approaches, bispecific antibodies (BsAbs) are of great interest due to their ability to recruit immune cells to kill tumor cells directly. Various BsAbs against Her2 tumor cells have been proposed with potent cytotoxic activities. However, most of these formats require extensive processing to obtain heterodimeric bispecific antibodies. In this study, we describe a bispecific antibody, BiHC (bispecific Her2-CD3 antibody), constructed with a single-domain anti-Her2 and a single-chain Fv (variable fragment) of anti-CD3 in an IgG-like format. In contrast to most IgG-like BsAbs, the two arms in BiHC have different molecular weights, making it easier to separate hetero- or homodimers. BiHC can be expressed in Escherichia coli and purified via Protein A affinity chromatography. The purified BiHC can recruit T cells and induce specific cytotoxicity of Her2-expressing tumor cells in vitro. The BiHC can also efficiently inhibit the tumor growth in vivo. Thus, BiHC is a promising candidate for the treatment of Her2-positive cancers.
在不同的癌症免疫治疗方法中,双特异性抗体(BsAbs)因其能够募集免疫细胞直接杀死肿瘤细胞而备受关注。已经提出了多种针对Her2肿瘤细胞的具有强大细胞毒性活性的双特异性抗体。然而,这些形式中的大多数都需要大量处理才能获得异源二聚体双特异性抗体。在本研究中,我们描述了一种双特异性抗体BiHC(双特异性Her2-CD3抗体),它以IgG样形式构建,包含一个抗Her2单域抗体和一个抗CD3单链Fv(可变片段)。与大多数IgG样双特异性抗体不同,BiHC的两条臂具有不同的分子量,这使得分离异源或同源二聚体更加容易。BiHC可以在大肠杆菌中表达,并通过蛋白A亲和层析进行纯化。纯化后的BiHC能够募集T细胞,并在体外诱导表达Her2的肿瘤细胞产生特异性细胞毒性。BiHC在体内也能有效抑制肿瘤生长。因此,BiHC是治疗Her2阳性癌症的一个有前景的候选药物。