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A Chicken Bioreactor for Efficient Production of Functional Cytokines

Overview
Journal BMC Biotechnol
Publisher Biomed Central
Specialty Biotechnology
Date 2018 Dec 31
PMID 30594166
Citations 19
Authors
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Abstract

Background: The global market for protein drugs has the highest compound annual growth rate of any pharmaceutical class but their availability, especially outside of the US market, is compromised by the high cost of manufacture and validation compared to traditional chemical drugs. Improvements in transgenic technologies allow valuable proteins to be produced by genetically-modified animals; several therapeutic proteins from such animal bioreactors are already on the market after successful clinical trials and regulatory approval. Chickens have lagged behind mammals in bioreactor development, despite a number of potential advantages, due to the historic difficulty in producing transgenic birds, but the production of therapeutic proteins in egg white of transgenic chickens would substantially lower costs across the entire production cycle compared to traditional cell culture-based production systems. This could lead to more affordable treatments and wider markets, including in developing countries and for animal health applications.

Results: Here we report the efficient generation of new transgenic chicken lines to optimize protein production in eggs. As proof-of-concept, we describe the expression, purification and functional characterization of three pharmaceutical proteins, the human cytokine interferon α2a and two species-specific Fc fusions of the cytokine CSF1.

Conclusion: Our work optimizes and validates a transgenic chicken system for the cost-effective production of pure, high quality, biologically active protein for therapeutics and other applications.

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References
1.
Massoud M, Attal J, Thepot D, Pointu H, Stinnakre M, Theron M . The deleterious effects of human erythropoietin gene driven by the rabbit whey acidic protein gene promoter in transgenic rabbits. Reprod Nutr Dev. 1996; 36(5):555-63. DOI: 10.1051/rnd:19960511. View

2.
Liang T, Rehermann B, Seeff L, Hoofnagle J . Pathogenesis, natural history, treatment, and prevention of hepatitis C. Ann Intern Med. 2000; 132(4):296-305. DOI: 10.7326/0003-4819-132-4-200002150-00008. View

3.
Dyck M, Lacroix D, Pothier F, Sirard M . Making recombinant proteins in animals--different systems, different applications. Trends Biotechnol. 2003; 21(9):394-9. DOI: 10.1016/S0167-7799(03)00190-2. View

4.
Yang C, Gao X, Gong R . Engineering of Fc Fragments with Optimized Physicochemical Properties Implying Improvement of Clinical Potentials for Fc-Based Therapeutics. Front Immunol. 2018; 8:1860. PMC: 5766897. DOI: 10.3389/fimmu.2017.01860. View

5.
Shukla A, Wolfe L, Mostafa S, Norman C . Evolving trends in mAb production processes. Bioeng Transl Med. 2018; 2(1):58-69. PMC: 5689530. DOI: 10.1002/btm2.10061. View