| Literature DB >> 33396657 |
Takehiro Mukae1, Sho Okumura2, Takuma Watanobe2, Kyoko Yoshii1, Takahiro Tagami3, Isao Oishi1.
Abstract
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.Entities:
Keywords: antibody production; bioreactor; chicken; genome editing; knock-in
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Year: 2020 PMID: 33396657 PMCID: PMC7823952 DOI: 10.3390/genes12010038
Source DB: PubMed Journal: Genes (Basel) ISSN: 2073-4425 Impact factor: 4.096