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可编程多特异性 DNA 折纸基 T 细胞衔接器。

Programmable multispecific DNA-origami-based T-cell engagers.

机构信息

Department of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.

Munich Institute of Biomedical Engineering, Technical University of Munich, Garching, Germany.

出版信息

Nat Nanotechnol. 2023 Nov;18(11):1319-1326. doi: 10.1038/s41565-023-01471-7. Epub 2023 Aug 17.

Abstract

Multispecific antibodies have emerged as versatile therapeutic agents, and therefore, approaches to optimize and streamline their design and assembly are needed. Here we report on the modular and programmable assembly of IgG antibodies, F(ab) and scFv fragments on DNA origami nanocarriers. We screened 105 distinct quadruplet antibody variants in vitro for the ability to activate T cells in the presence of target cells. T-cell engagers were identified, which in vitro showed the specific and efficient T-cell-mediated lysis of five distinct target cell lines. We used these T-cell engagers to target and lyse tumour cells in vivo in a xenograft mouse tumour model. Our approach enables the rapid generation, screening and testing of bi- and multispecific antibodies to facilitate preclinical pharmaceutical development from in vitro discovery to in vivo proof of concept.

摘要

多特异性抗体已经成为多功能治疗药物,因此需要优化和简化其设计和组装的方法。在这里,我们报告了在 DNA 折纸纳米载体上对 IgG 抗体、F(ab)和 scFv 片段进行模块化和可编程组装的方法。我们在体外筛选了 105 种不同的四联体抗体变体,以评估它们在存在靶细胞的情况下激活 T 细胞的能力。鉴定出了 T 细胞激活剂,这些激活剂在体外能够特异性和有效地介导五种不同靶细胞系的 T 细胞杀伤。我们使用这些 T 细胞激活剂在异种移植小鼠肿瘤模型中靶向和杀伤肿瘤细胞。我们的方法能够快速生成、筛选和测试双特异性和多特异性抗体,从而促进从体外发现到体内验证概念的临床前药物开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d83/10656288/00e10bee5998/41565_2023_1471_Fig1_HTML.jpg

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