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一种用于发现和优化双特异性免疫结合抗体的简化功能优先方法。

A simplified function-first method for the discovery and optimization of bispecific immune engaging antibodies.

机构信息

Human Health Therapeutics Research Centre, National Research Council, Ottawa, Canada.

Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada.

出版信息

PLoS One. 2023 Jun 22;18(6):e0273884. doi: 10.1371/journal.pone.0273884. eCollection 2023.

Abstract

Bi-specific T-cell engager antibodies (BiTEs) are synthetic fusion molecules that combine multiple antibody-binding domains to induce active contact between T-cells and antigen expressing cells in the body. Blinatumomab, a CD19-CD3 BiTE is now a widely used therapy for relapsed B-cell malignancies, and similar BiTE therapeutics have shown promise for treating various other forms of cancer. The current process for new BiTE development is time consuming and costly, requiring characterization of the individual antigen binding domains, followed by bi-specific design, protein production, purification, and eventually functional screening. Here, we sought to establish a more cost-efficient approach for generating novel BiTE sequences and assessing bioactivity through a function first approach without purification. We generate a plasmid with a bi-modular structure to allow high-throughput exchange of either binding arm, enabling rapid screening of novel tumour-targeting single chain variable (scFv) domains in combination with the well-characterized OKT3 scFv CD3-targeting domain. We also demonstrate two systems for high throughput functional screening of BiTE proteins based on Jurkat T cells (referred to as BiTE-J). Using BiTE-J we evaluate four EGFRvIII-scFv sequenced in BiTE format, identifying two constructs with superior activity for redirecting T-cells against the EGFRvIII-tumour specific antigen. We also confirm activity in primary T cells, where novel EGFRvIII-BiTEs induced T cell activation and antigen selective tumor killing. We finally demonstrate similar exchange the CD3-interacting element of our bi-modular plasmid. By testing several novel CD3-targeting scFv elements for activity in EGFRvIII-targeted BiTEs, we were able to identify highly active BiTE molecules with desirable functional activity for downstream development. In summary, BiTE-J presents a low cost, high-throughput method for the rapid assessment of novel BiTE molecules without the need for purification and quantification.

摘要

双特异性 T 细胞衔接抗体(BiTEs)是一种合成融合分子,它结合了多个抗体结合结构域,以诱导体内 T 细胞与表达抗原的细胞之间的主动接触。blinatumomab 是一种 CD19-CD3 BiTE,现已广泛用于治疗复发性 B 细胞恶性肿瘤,类似的 BiTE 疗法已显示出治疗各种其他形式癌症的潜力。目前的新 BiTE 开发过程既耗时又昂贵,需要对各个抗原结合结构域进行表征,然后进行双特异性设计、蛋白质生产、纯化,最终进行功能筛选。在这里,我们试图通过不进行纯化的功能优先方法,建立一种更具成本效益的方法来生成新型 BiTE 序列并评估其生物活性。我们生成了一种带有双模块结构的质粒,允许高通量交换任一个结合臂,从而能够快速筛选与经过充分表征的 OKT3 scFv CD3 靶向结构域相结合的新型肿瘤靶向单链可变(scFv)结构域。我们还展示了两种基于 Jurkat T 细胞的高通量 BiTE 蛋白功能筛选系统(称为 BiTE-J)。使用 BiTE-J,我们评估了以 BiTE 形式排列的四个 EGFRvIII-scFv,确定了两种针对 EGFRvIII-肿瘤特异性抗原重新定向 T 细胞的构建体,具有更高的活性。我们还在原代 T 细胞中证实了其活性,其中新型 EGFRvIII-BiTE 诱导了 T 细胞的激活和抗原选择性肿瘤杀伤。我们最后证明了类似的方法可以交换我们的双模块质粒的 CD3 相互作用元件。通过测试几种新型 CD3 靶向 scFv 元件在 EGFRvIII 靶向 BiTE 中的活性,我们能够鉴定出具有理想功能活性的高活性 BiTE 分子,以进行下游开发。总之,BiTE-J 提供了一种低成本、高通量的方法,可以快速评估新型 BiTE 分子,而无需进行纯化和定量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5031/10286961/b335fd512c94/pone.0273884.g001.jpg

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