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从重组IgG1抗体生成T细胞依赖性双特异性构建体的模块化半合成方法。

Modular Semisynthetic Approach to Generate T Cell-Dependent Bispecific Constructs from Recombinant IgG1 Antibodies.

作者信息

Shajan Irene, Rochet Léa N C, Tracey Shannon R, Benazza Rania, Jackowska Bianka, Hernandez-Alba Oscar, Cianférani Sarah, Scott Christopher J, van Delft Floris L, Chudasama Vijay, Albada Bauke

机构信息

Laboratory of Organic Chemistry, Wageningen University & Research, Stippeneng 4, Wageningen 6807 WE, The Netherlands.

Department of Chemistry, University College London, 20 Gordon St, London WC1H 0AJ, United Kingdom.

出版信息

Bioconjug Chem. 2024 Sep 16;35(10):1524-31. doi: 10.1021/acs.bioconjchem.4c00309.

Abstract

Redirecting T cells to tumor cells by bispecific antibodies is an effective approach to treat cancer, and T cell-dependent bispecific antibodies (TDBAs) are an emerging class of potent immunotherapeutic agents. By simultaneously targeting antigens on tumor cells and T cells, T cells are activated to kill tumor cells. Herein, we report a platform to generate a novel class of 2:1 structure of T cell-dependent bispecific antibody with bivalency for HER2 receptors on tumor cells and monovalency for CD3 receptors on T cells. For this, we use a biogenic inverse electron-demand Diels-Alder (IEDDA) click reaction on genetically encoded tyrosine residues to install one TCO handle on therapeutically approved antibody trastuzumab. Subsequent TCO-tetrazine click with a tetrazine-functionalized CD3-binding Fab yields a 2:1 HER2 × CD3 TDBA that exhibits a tumor-killing capability at picomolar concentrations. Monovalency toward the CD3 receptor on T cells can lower the chances of cytokine release syndrome, which is a common side effect of such agents. Our semisynthetic approach can generate highly potent TDBA constructs in a few chemoenzymatic and synthetic steps.

摘要

通过双特异性抗体将T细胞重定向至肿瘤细胞是一种治疗癌症的有效方法,而T细胞依赖性双特异性抗体(TDBA)是一类新兴的强效免疫治疗药物。通过同时靶向肿瘤细胞和T细胞上的抗原,激活T细胞以杀死肿瘤细胞。在此,我们报告了一个平台,用于生成一类新型的2:1结构的T细胞依赖性双特异性抗体,其对肿瘤细胞上的HER2受体具有双价性,对T细胞上的CD3受体具有单价性。为此,我们在基因编码的酪氨酸残基上使用生物正交的逆电子需求狄尔斯-阿尔德(IEDDA)点击反应,在治疗上已获批准的抗体曲妥珠单抗上安装一个反式环辛烯(TCO)手柄。随后,TCO与四嗪功能化的CD3结合Fab进行四嗪点击反应,产生一种2:1 HER2×CD3 TDBA,其在皮摩尔浓度下表现出肿瘤杀伤能力。对T细胞上CD3受体的单价性可降低细胞因子释放综合征的发生几率,而细胞因子释放综合征是此类药物常见的副作用。我们的半合成方法可以通过几个化学酶促和合成步骤生成高效的TDBA构建体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c74a/11487494/132cb68a13d1/bc4c00309_0003.jpg

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