Development of Plant-Derived Bispecific Monoclonal Antibody Targeting PD-L1 and CTLA-4 against Mouse Colorectal Cancer.

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL
Planta medica Pub Date : 2024-04-01 Epub Date: 2024-02-19 DOI:10.1055/a-2240-7534
Christine Joy I Bulaon, Narach Khorattanakulchai, Kaewta Rattanapisit, Hongyan Sun, Nuttapat Pisuttinusart, Waranyoo Phoolcharoen
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引用次数: 0

Abstract

Checkpoint blockade immunotherapy has revolutionized cancer treatment, with monoclonal antibodies targeting immune checkpoints, yielding promising clinical benefits. However, with the advent of resistance to immune checkpoint inhibitor treatment in clinical trials, developing next-generation antibodies with potentially increased efficacy is critical. Here, we aimed to generate a recombinant bispecific monoclonal antibody for dual inhibition of programmed cell death protein 1/programmed cell death ligand 1 and cytotoxic T-lymphocyte-associated protein 4 axes. The plant system was used as an alternative platform for bispecific monoclonal antibody production. Dual variable domain immunoglobulin atezolizumab × 2C8 is a plant-derived bispecific monoclonal antibody that combines both programmed cell death ligand 1 and cytotoxic T-lymphocyte-associated protein 4 blockade into a single molecule. Dual variable domain immunoglobulin atezolizumab × 2C8 was transiently expressed in Nicotiana benthamiana and the expression level was determined to be the highest after 4 days of infiltration. The size and assembly of the purified bispecific monoclonal antibody were determined, and its function was investigated in vitro and in vivo. The molecular structures of plant-produced dual variable domain immunoglobulin atezolizumab × 2C8 are as expected, and it was mostly present as a monomer. The plant-produced dual variable domain immunoglobulin atezolizumab × 2C8 showed in vitro binding to programmed cell death ligand 1 and cytotoxic T-lymphocyte-associated protein 4 proteins. The antitumor activity of plant-produced bispecific monoclonal antibody was tested in vivo by treating humanized Balb/c mice bearing a CT26 colorectal tumor. Plant-produced dual variable domain immunoglobulin atezolizumab × 2C8 significantly inhibited tumor growth by reducing tumor volume and weight. Body weight changes indicated that the plant-produced bispecific monoclonal antibody was safe and tolerable. Overall, this proof of concept study demonstrated the viability of plants to produce functional plant-based bispecific immunotherapy.

开发针对小鼠结直肠癌的 PD-L1 和 CTLA-4 植物衍生双特异性单克隆抗体
检查点阻断免疫疗法为癌症治疗带来了革命性的变化,针对免疫检查点的单克隆抗体取得了可喜的临床疗效。然而,随着临床试验中出现对免疫检查点抑制剂治疗的耐药性,开发具有潜在增效作用的下一代抗体至关重要。在这里,我们旨在生成一种重组双特异性单克隆抗体,用于程序性细胞死亡蛋白1/程序性细胞死亡配体1和细胞毒性T淋巴细胞相关蛋白4轴的双重抑制。植物系统被用作生产双特异性单克隆抗体的替代平台。双可变域免疫球蛋白atezolizumab×2C8是一种植物衍生的双特异性单克隆抗体,它将程序性细胞死亡配体1和细胞毒性T淋巴细胞相关蛋白4阻断作用结合到一个分子中。双可变结构域免疫球蛋白 atezolizumab × 2C8 在烟草中瞬时表达,并在浸润 4 天后确定其表达水平最高。测定了纯化的双特异性单克隆抗体的大小和组装情况,并对其体外和体内功能进行了研究。植物生产的双可变结构域免疫球蛋白 atezolizumab × 2C8 的分子结构符合预期,且大部分以单体形式存在。植物生产的双可变域免疫球蛋白 atezolizumab × 2C8 在体外与程序性细胞死亡配体 1 和细胞毒性 T 淋巴细胞相关蛋白 4 蛋白结合。通过对携带 CT26 大肠肿瘤的人源化 Balb/c 小鼠进行治疗,对植物生产的双特异性单克隆抗体的抗肿瘤活性进行了体内测试。植物生产的双可变域免疫球蛋白 atezolizumab × 2C8 通过减少肿瘤体积和重量显著抑制了肿瘤的生长。体重变化表明,植物生产的双特异性单克隆抗体是安全和可耐受的。总之,这项概念验证研究证明了植物生产功能性植物双特异性免疫疗法的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
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