Plant-based vaccines: The way ahead?

, , & (2021) Plant-based vaccines: The way ahead? Viruses, 13(1), Article number: 5.

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Severe virus outbreaks are occurring more often and spreading faster and further than ever. Preparedness plans based on lessons learned from past epidemics can guide behavioral and pharmacological interventions to contain and treat emergent diseases. Although conventional bi-ologics production systems can meet the pharmaceutical needs of a community at homeostasis, the COVID-19 pandemic has created an abrupt rise in demand for vaccines and therapeutics that highlight the gaps in this supply chain’s ability to quickly develop and produce biologics in emergency situations given a short lead time. Considering the projected requirements for COVID-19 vaccines and the necessity for expedited large scale manufacture the capabilities of current biologics production systems should be surveyed to determine their applicability to pandemic preparedness. Plant-based biologics production systems have progressed to a state of commercial viability in the past 30 years with the capacity for production of complex, glycosylated, “mammalian compatible” molecules in a system with comparatively low production costs, high scalability, and production flexibility. Continued research drives the expansion of plant virus-based tools for harnessing the full production capacity from the plant biomass in transient systems. Here, we present an overview of vaccine production systems with a focus on plant-based production systems and their potential role as “first responders” in emergency pandemic situations.

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26 citations in Scopus
21 citations in Web of Science®
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ID Code: 229396
Item Type: Contribution to Journal (Review article)
Refereed: Yes
ORCID iD:
Bally, Juliaorcid.org/0000-0003-0692-280X
Additional Information: Funding Information: Funding: This work was funded by the Australian Research Council (ARC), grant number FL16010 0155 and DP170103960.
Measurements or Duration: 13 pages
Keywords: Biopharming, COVID-19, Nicotiana benthamiana, Plant-based biologics production, Vaccines, Viral vectors, Viruses
DOI: 10.3390/v13010005
ISSN: 1999-4915
Pure ID: 107642919
Divisions: Current > Research Centres > Centre for Agriculture and the Bioeconomy
Current > QUT Faculties and Divisions > Faculty of Science
Current > Schools > School of Biology & Environmental Science
Funding Information: Funding: This work was funded by the Australian Research Council (ARC), grant number FL16010 0155 and DP170103960. Despite a modest presence of products on the pharmaceutical market, plant bio-pharming systems have been demonstrated on several occasions to be effective biologics production hosts, with the full capacity to produce correctly folded and glycosylated therapeutic molecules. In 2001, the Blue Angel Project sponsored by the US Defense Advanced Research Projects Agency sought to address, “insufficient capability to provide vaccines against pandemics caused by new strains, as well as infections caused by intentional bio-threats”, by demonstrating the vaccine production capabilities of plant-based systems, by 1. developing a hardened, high containment, self-sufficient plant-based pharmaceutical production facility; 2. building a facility with the capacity to manufacture 10 million doses of an H1N1 influenza vaccine in a single month; and 3. completing this project within an 18 month window [72]. This project demonstrated that the plant-based production systems were capable of quick vaccine production and have the production pace that would be required to quell an unexpected viral outbreak. It was successfully completed in different stages by Medicago Inc., Caliber Biotherapeutics Inc. (now iBio Inc.), Fraunhofer CMB and Kentucky BioProcessing Inc. These companies operate currently as producers of biologics with portfolios including various vaccines and/or antibodies for cancer therapies. Today, Medicago reports that it can deliver mass quantities of a novel flu vaccine in a three-month timeline [73]. In 2014, The production speed of this system was demonstrated when Kentucky BioProcessing was able to quickly produce an Ebola antibody cocktail called Zmapp, developed by Mapp Biopharmaceutical, that had been granted emergency compassionate approval for human use [74]. This product, which is administered at 50 mg/kg, was produced in sufficient quantities to be used for the treatment of six people infected with Ebola, five of whom recovered. More recently, Medicago was able to produce VLP vaccine candidates 20 days after having access to the COVID-19 S protein sequence [75]. Although the long duration of clinical trials cannot be avoided, emergency governmental authorization to overlap clinical trials can shorten time to deployment for vaccines; making vaccine development and production timelines the bottlenecks prolonging the time to deployment [76].
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Copyright Owner: 2020 by the authors
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Deposited On: 06 Apr 2022 03:03
Last Modified: 03 Aug 2024 03:18