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Summary
February 2005, Vol. 10, No. 1, Pages 185-218
, DOI 10.1517/14728214.10.1.185
Transgenic plants in the biopharmaceutical marketRichard M TwymanUniversity of York, Department of Biology, Heslington, York YO10 5DD, UK. richard@writescience.com Many of our ‘small-molecule-drugs’ are natural products from plants, or are synthetic compounds based on molecules found naturally in plants. However, the vast majority of the protein therapeutics (or biopharmaceuticals) we use are from animal or human sources, and are produced commercially in microbial or mammalian bioreactor systems. Over the last few years, it has become clear that plants have great potential for the production of human proteins and other protein-based therapeutic entities. Plants offer the prospect of inexpensive biopharmaceutical production without sacrificing product quality or safety, and following the success of several plant-derived technical proteins, the first therapeutic products are now approaching the market. In this review, the different plant-based production systems are discussed and the merits of transgenic plants are evaluated compared with other platforms. A detailed discussion is provided of the development issues that remain to be addressed before plants become an acceptable mainstream production technology. The many different proteins that have already been produced using plants are described, and a sketch of the current market and the activities of the key players is provided. Despite the currently unclear regulatory framework and general industry inertia, the benefits of plant-derived pharmaceuticals are now bringing the prospect of inexpensive veterinary and human medicines closer than ever before. Forward Links to Citing ArticlesM. O’Brien, E. Mullins. (2009) Relevance of genetically modified crops in light of future environmental and legislative challenges to the agri-environment. Annals of Applied Biology 154:3, 323-340 Online publication date: 1-Jul-2009. CrossRef Vidadi Yusibov, Shailaja Rabindran. (2008) Recent progress in the development of plant derived vaccines. Expert Review of Vaccines 7:8, 1173-1183 Online publication date: 1-Nov-2008. CrossRef Koreen Ramessar, Teresa Capell, Paul Christou. (2008) Molecular pharming in cereal crops. Phytochemistry Reviews 7:3, 579-592 Online publication date: 1-Nov-2008. CrossRef Francesca Pizzuti, Lorenza Daroda. (2008) Investigating recombinant protein exudation from roots of transgenic tobacco. Environmental Biosafety Research 7:4, 219-226 Online publication date: 1-Nov-2008. CrossRef Meriem Benchabane, Charles Goulet, Daniel Rivard, Loïc Faye, Véronique Gomord, Dominique Michaud. (2008) Preventing unintended proteolysis in plant protein biofactories. Plant Biotechnology Journal 6:7, 633-648 Online publication date: 1-Oct-2008. CrossRef Lina Wang, Ross L Coppel. (2008) Oral vaccine delivery: can it protect against non-mucosal pathogens?. Expert Review of Vaccines 7:6, 729-738 Online publication date: 1-Sep-2008. CrossRef K. Ramessar, T. Rademacher, M. Sack, J. Stadlmann, D. Platis, G. Stiegler, N. Labrou, F. Altmann, J. Ma, E. Stoger, T. Capell, P. Christou. (2008) Cost-effective production of a vaginal protein microbicide to prevent HIV transmission. Proceedings of the National Academy of Sciences 105:10, 3727-3732 Online publication date: 11-Apr-2008. CrossRef Penelope Amelia Claire Sparrow, Judith A. Irwin, Phil J. Dale, Richard M. Twyman, Julian K. C. Ma. (2007) Pharma-Planta: road testing the developing regulatory guidelines for plant-made pharmaceuticals. Transgenic Research 16:2, 147 CrossRef Vadim Mett, Abdel-Moneim Shamloul, Hiroki Hirai, Zhaohua Zhou, Abner Notkins, Vidadi Yusibov. (2007) Engineering and expression of the intracellular domain of insulinoma-associated tyrosine phosphatase (IA-2ic), a type 1 diabetes autoantigen, in plants. Transgenic Research 16:1, 77 CrossRef Julian K -C. Ma, Eugenia Barros, Ralph Bock, Paul Christou, Philip J. Dale, Philip J. Dix, Rainer Fischer, Judith Irwin, Richard Mahoney, Mario Pezzotti. (2005) Molecular farming for new drugs and vaccines. EMBO Reports 6:7, 593 CrossRef DWAYNE KIRK, JASON SCOTT ROBERT. (2005) Assessing Commercial Feasibility: A Practical and Ethical Prerequisite for Human Clinical Testing. Accountability in Research Policies and Quality Assurance 12:4, 281 CrossRef Stephen J Streatfield. (2005) Regulatory issues for plant-made pharmaceuticals and vaccines. Expert Review of Vaccines 4:4, 591 CrossRef Dwayne D. Kirk, Kim McIntosh, Amanda M Walmsley, Robert K. D. Peterson. (2005) Risk analysis for plant-made vaccines. Transgenic Research 14:4, 449 CrossRef |
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