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Production of Recombinant Monoclonal Antibodies in the Egg White of Gene-Targeted Transgenic Chickens

机译:基因靶向转基因鸡的蛋白中重组单克隆抗体的生产

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摘要

Increased commercial demand for monoclonal antibodies (mAbs) has resulted in the urgent need to establish efficient production systems. We previously developed a transgenic chicken bioreactor system that effectively produced human cytokines in egg whites using genome-edited transgenic chickens. Here, we describe the application of this system to mAb production. The genes encoding the heavy and light chains of humanized anti-HER2 mAb, linked by a 2A peptide sequence, were integrated into the chicken ovalbumin gene locus using a CRISPR/Cas9 protocol. The knock-in hens produced a fully assembled humanized mAb in their eggs. The mAb expression level in the egg white was 1.4–1.9 mg/mL, as determined by ELISA. Furthermore, the antigen binding affinity of the anti-HER2 mAb obtained was estimated to be equal to that of the therapeutic anti-HER2 mAb (trastuzumab). In addition, antigen-specific binding by the egg white mAb was demonstrated by immunofluorescence against HER2-positive and -negative cells. These results indicate that the chicken bioreactor system can efficiently produce mAbs with antigen binding capacity and can serve as an alternative production system for commercial mAbs.
机译:增加对单克隆抗体(MAB)的商业需求导致迫切需要建立有效的生产系统。我们以前开发了一种转基因鸡生物反应器系统,可使用基因组编辑的转基因鸡在蛋清中有效地产生人细胞因子。在这里,我们描述了该系统将该系统应用于MAB生产。编码由2A肽序列连接的人源化抗HER -2 mAb的重链和灯链的基因,使用CRISPR / CAS9方案整合到鸡卵磷酸基因基因座中。敲门母鸡在其卵中产生了完全组装的人源化的mAb。蛋白中的MAb表达水平为1.4-1.9mg / ml,由ELISA测定。此外,估计所得抗HER2 mAb的抗原结合亲和力等于治疗性抗HER2 mAb(曲妥珠单抗)的抗原结合亲和力。此外,通过免疫荧光对HER2阳性和阴性细胞进行抗原特异性的蛋白mAb结合。这些结果表明,鸡生物反应器系统可以有效地产生具有抗原结合能力的MAb,并且可以作为商业MAB的替代生产系统。

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