Next Article in Journal
Parallel Reaction Monitoring: A Targeted Experiment Performed Using High Resolution and High Mass Accuracy Mass Spectrometry
Next Article in Special Issue
Cissus sicyoides: Pharmacological Mechanisms Involved in the Anti-Inflammatory and Antidiarrheal Activities
Previous Article in Journal
Repositioning of Thiourea-Containing Drugs as Tyrosinase Inhibitors
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Plants as Factories for Human Pharmaceuticals: Applications and Challenges

Emergency Department, The Affiliated Hospital of Qingdao University, Qingdao 266003, China
Department of Natural Sciences Northeastern State University at Broken Arrow, Broken Arrow, OK 74014, USA
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2015, 16(12), 28549-28565;
Received: 19 September 2015 / Revised: 18 November 2015 / Accepted: 23 November 2015 / Published: 2 December 2015
(This article belongs to the Special Issue Plant-Derived Pharmaceuticals by Molecular Farming 2016)


Plant molecular farming (PMF), defined as the practice of using plants to produce human therapeutic proteins, has received worldwide interest. PMF has grown and advanced considerably over the past two decades. A number of therapeutic proteins have been produced in plants, some of which have been through pre-clinical or clinical trials and are close to commercialization. Plants have the potential to mass-produce pharmaceutical products with less cost than traditional methods. Tobacco-derived antibodies have been tested and used to combat the Ebola outbreak in Africa. Genetically engineered immunoadhesin (DPP4-Fc) produced in green plants has been shown to be able to bind to MERS-CoV (Middle East Respiratory Syndrome), preventing the virus from infecting lung cells. Biosafety concerns (such as pollen contamination and immunogenicity of plant-specific glycans) and costly downstream extraction and purification requirements, however, have hampered PMF production from moving from the laboratory to industrial application. In this review, the challenges and opportunities of PMF are discussed. Topics addressed include; transformation and expression systems, plant bioreactors, safety concerns, and various opportunities to produce topical applications and health supplements.

Graphical Abstract

1. Introduction

The production of plant-derived pharmaceuticals has attracted great interest. Mapp Biopharmaceutical Inc., a company located in San Diego, CA, USA has produced a drug in tobacco leaves called ZMapp, which has been used to combat the 2014 Ebola virus outbreak in Africa [1]. As of October 2014, seven infected patients received an early treatment with ZMapp and fully recovered. Another patient, receiving a late treatment with ZMapp in November 2014, however, succumbed to the disease and died. Additional Ebola patients were unable to receive the treatment due to an insufficient supply of ZMapp. This is unfortunate since it is the only drug to date that has been effectively used to treat patients infected with the Ebola virus, even though it has not been approved by the U.S. Food and Drug Administration (FDA). ZMapp has been subjected to clinical Phase I and 2 trials in 2015, sponsored by the National Institute of Allergy and Infectious Diseases (NIAID) (see Table 1). On 15 September 2015, ZMapp was granted a fast track status by the FDA [2]. Middle East respiratory syndrome coronavirus (MERS-CoV) is an emerging disease. Due to the high mortality rate of MERS (above 35%), it caused a public panic in South Korea during May 2015. As of 27 November 2015, MERS-CoV has infected 1618 patients and caused a total of 579 deaths worldwide. Over 26 countries have reported MERS-CoV cases [3]. Currently, no effective drug is available to treat the MERS-CoV virus. Plant Biotechnology Inc. (Hayward, CA, USA) produced an immunoadhesin (DPP4-Fc) in transgenic tobacco. Purified DPP4-Fc exhibits strong binding to MERS-CoV and prevents the virus from infecting lung cells. In June 2015, Plant Biotechnology Inc. received funding from NIAID to support further development and testing of this drug [4].
The concept of using plants to produce recombinant pharmaceutical proteins, referred to as plant molecular farming (PMF) or pharming (PMP), is not new. Human growth hormone, initially produced in tobacco and sunflower in 1986, was the first-plant-derived recombinant therapeutic protein [5]. Mason et al. [6] later expressed the hepatitis B surface antigen (HBsAg) in transgenic tobacco. This plant-derived antigen was physically and antigenically similar to the HBsAg obtained from human serum and recombinant yeast. The yeast-derived HBsAg is clinically used for HBV vaccination. Since 1994, more than 100 pharmaceutical proteins have been expressed and characterized in plants. By 2011, more than twenty PMF pharmaceuticals were placed in preclinical or clinical trials [7]. Several PMF products have completed Phase 2 trials and one product has been approved by the FDA (Table 1). Although several plant-derived drugs have been commercialized as research and diagnostic reagents (such as tobacco derived aprotinin and rice derived lysozyme from Sigma-Aldrich Company (St. Louis, MO, USA) or received USDA approval as a vaccine additive for use in poultry (Dow Agro Sciences, Indianapolis, IN, USA) [1], the current review mainly focuses on PMF in relation to human pharmaceutical applications. Plants represent a promising system for the production of human pharmaceutical proteins on a large scale, and at a low cost. Many production challenges, however, such as low yield [7,8,9,10], plant glycosylation [11,12,13], purification and downstream processing hurdles [14,15,16], have limited the development of PMF-based human pharmaceuticals on a clinical scale.
In May 2012, the first PMF-derived enzyme, ELELYSO™ (taliglucerase alfa) (Protalix BioTherapeutics, Karmiel, Israel), was approved for human use by the FDA [17]. ELELYSO™ is based on the use of carrot cells to produce recombinant taliglucerase alfa, which is used in an enzyme replacement therapy to treat adult patients with Gaucher disease. The production and application of ELELYSO™, however, is not representative of other PMF-derived pharmaceuticals for several reasons. Since Gaucher disease is a rare genetic disease, mostly found among Ashkenazi Jews, ELELYSO™ has limited production needs. The FDA also accelerated (fast tracked) the approval process as a treatment for a rare disease. Additionally, the drug is produced in carrot cells using a large bioreactor under very stringent conditions. This process is different from production of other PMF products, which generally use entire leaves, fruits, seeds, or whole plants to produce the recombinant pharmaceutical. The production and approval of ELELYSO™ still represents a major step forward for the whole field of PMF. Many companies have now explored and started product pipelines utilizing plant-expression systems (see Table 2).
Identifying potential genes suitable for PMF and general approaches is becoming more simple and straight forward. Facilitated by the rapid progress in genomics, proteomics, and bioinformatics, a greater number of useful genes are being identified and characterized. Additionally, relatively routine molecular methods have become available for placing the genes of interest into plant expression vectors and transforming them into plants (see Figure 1).
Table 1. Examples of plant-derived pharmaceuticals in clinical trials (data from U.S. National Institutes of Health Clinical Trial [18].
Table 1. Examples of plant-derived pharmaceuticals in clinical trials (data from U.S. National Institutes of Health Clinical Trial [18].
ProductHostApplicationClinical TrialStatusSponsor
Taliglucerase alfa;
Recombinant glucocerebrosidase (prGCD)
Carrot cell cultureGaucher diseaseNCT00376168Phase 3 completed (2012);
FDA approved (2012)
Protalix, Karmiel, Israel
ZMAppTobaccoEbola VirusNCT02363322Phase 1 and 2 (2015)National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD, USA
PRX-102Tobacco cell cultureFabry DiseaseNCT01769001Phase 1 and 2 (2014)Protalix, Karmiel, Israel
VaccinePfs25 VLPTobaccoMalariaNCT02013687Phase 1 (2015)Center for Molecular Biotechnology, Plymouth, MI, USA
Vaccine Recombinant protective antigenTobaccoAnthraxNCT02239172Phase 1 (2014)Center for Molecular Biotechnology, Plymouth, MI, USA
HAI-05TobaccoH5N1 VaccineNCT01250795Phase 1 (2011)Center for Molecular Biotechnology, Plymouth, MI, USA
Recombinant human intrinsic factorArabidopsis thalianaVitamin B12 deficiencyNCT00279552Phase 2 Completed (2006)University in Aarhus, Aarhus, Denmark
H5-VLP + GLA-AF VaccineTobaccoInfluenza A Subtype H5N1 InfectionNCT01657929Phase 1 Completed (2014)Infectious Disease Research Institute, Seattle, WA, USA
P2G12 AntibodyTobaccoHIVNCT01403792Phase 1 Completed (2011)University of Surrey, Guildford, UK
Table 2. Examples of companies utilizing PMF to produce human pharmaceuticals (data from company websites).
Table 2. Examples of companies utilizing PMF to produce human pharmaceuticals (data from company websites).
CompanyHostLead ProductExpression TechnologyAdvantageWebsite References
Mapp Biopharmaceutical/LeafBiol, USATobacco leavesZMapp™ for Ebola crisisMagnICON Transient expressionSpeed[2]
Protalix, Carmiel, IsraelCarrot or tobacco cell cultureELELYSO™ (taliglucerase alfa) Enzyme replacementProCellEx® Stable ExpressionQuality[19]
Icon Genetics, München, GermanyNicotiana benthamiana leavesVaccine for non-Hodgkin’s LymphomaMagnICON Transient expressionSpeed and Personalization[20]
Ventria Bioscience, Junction City, KS, USARice seedsVEN150 for HIV-associated chronic inflammationExpress Tec Stable ExpressionScale Cost[21]
Greenovation Biotech GmbH, Heilbronn, GermanyMossMoss-GAA for Pompe Disease, Moss-GBA for Gaucher’s Disease, Moss-AGAL for Fabry DiseaseMoss Physcomitrella patens based BroytechnolgySpeed Scale and Customized[22]
Kentucky BioProcessing, Owensboro, KY, USANicotiana benthamiana leavesContract serviceGeneware Transient expressionSpeed[23]
PhycoBiologics Inc. Bloomington, IN, USAAlgaeVaccines Growth Factor and enzymesMicroalgae expressionSpeed Scale[24]
Medicago, Québec, QC, CanadaNicotiana benthamiana AlfalfaVaccine for influenza, Pandemic market, Rabies and RotavirusProficia™ Transient Expression; Stable ExpressionSpeed[25]
Synthon, Nijmegen, The NetherlandsDuckweed LeafyBiomassAntibody for non-Hodgkin’s LymphomaLEX system Stable expressionSpeed Quality[26]
Fraunhofer IME, Aachen, GermanyTobacco leavesHIV AntibodyStable Nuclear ExpressionScale Cost[27]
Fraunhofer CMB/iBio, Newark, DE, USANicotiana benthamiana leavesInfluenza vaccineTransient expressionSpeed[28]
Healthgen, Wuhan, Hubei, ChinaRice seedSerum albuminStable ExpressionQuality Scale[29]
PlanetBiotechnology, Hayward, CA, USATobacco leavesCaroRx for dental caries; PBI-220 antibody for anthrax; DPP4-Fc for MERS coronavirus infectionStable ExpressionQuality Scale[4]
Figure 1. Diagrammatic illustration of the process of Plant Molecular Farming (PMF).
Figure 1. Diagrammatic illustration of the process of Plant Molecular Farming (PMF).
Ijms 16 26122 g001
An example of an early proof of concept for PMF is the production of plant-derived edible human vaccines, using leafy plants or fruits [30,31,32,33,34,35]. Edible vaccines are an ideal product in concept since the vaccine could be administered to people orally, theoretically without the need of professional health care workers or sterile injections. The tedious and complicated process of purifying and storing the vaccine would also be eliminated since the food product itself would be the vaccine. The plants could also be grown locally, thus negating the cost of long distance transportation and storage. Edible vaccines also avoid the potential risk of infecting patients with a contaminated product since, in general, organisms causing plant diseases do not infect humans. The edible vaccine concept was first proposed by Charles Arntzen and coworkers, after HBsAg (Hepatitis B Virus antigen) was produced in tobacco plants. Mice fed HBsAg-transgenic potatoes exhibited a robust immune response [36]. Uncooked potatoes from transgenic potato plants producing HBsAg were later tested orally in humans. Greater than 60% of the volunteers exhibited strong systemic and mucosal immunity after three doses of potato were consumed [37]. These results demonstrated that plant-edible vaccines could be used in global immunization projects at a low cost. Subsequently, many other vaccine genes were expressed in a variety of crops, including lettuce, banana, and tomato fruits. Several plant vaccines are now in clinical trials that have produced encouraging data [38]. PMF production strategies and challenges, such as biosafety, appropriate expression systems, possible and potential applications, are discussed in the present review with the idea of demonstrating a feasible approach for the potential commercialization of a PMF product.

2. Advantages

A very advantageous aspect of PMF research is that it does not require a large financial investment to conduct initial studies. Plants can be grown in a greenhouse or even in a biosafety lab if required. The cost of plant maintenance for PMF is low, relative to E. coli, yeast, or mammalian cell expression systems (see Table 3); and the source (plant leaves or seeds) for making the recombinant protein is potentially unlimited [7,8,35]. Plant expression systems have several major advantages over prokaryotic and other eukaryotic cell systems in regards to production speed, cost, and safety. Plants can correctly fold and assemble complex proteins, such as secretory antibodies, full size immunoglobulins and the homodimeric vascular endothelial growth factor (VEGF). Human VEGF produced in barley grain has been commercialized for research use [39,40]. Plant-expressed human VEGF is used as treatment for thinning hair (UNICO Enterprises, Pasadena, CA, USA). Plants also have the capacity to introduce post-translational modifications. The use of plants also eliminates potential contamination of the therapeutic drug with animal pathogens (prions, viruses, and mycoplasmas), thus increasing safety. In general, the cost of PMF-derived products is only 0.1% of mammalian cell culture systems and 2%–10% of microbial systems.
Table 3. Comparison of different expression platforms for the production of pharmaceuticals (modified from Spök and Karner 2008 [41], European Communities).
Table 3. Comparison of different expression platforms for the production of pharmaceuticals (modified from Spök and Karner 2008 [41], European Communities).
ComparisonsTransgenic PlantPlant Cell CultureBacteriaYeastMammalian Cell CultureTransgenic Animals
Overall costVery lowMediumLowMediumHighHigh
Scale-up capacityVery highMediumHighHighVery lowLow
Production scaleWorldwideLimitedLimitedLimitedLimitedLimited
Protein yieldHighHighMediumHighMedium-HighHigh
Protein folding accuracyHighHighLowMediumHighHigh
GlycosylationMinor differencesMinor differencesNoneIncorrectCorrectCorrect
Product qualityHighHighLowMediumHighHigh
Contamination risksLow LowEndotoxinsLowVirus, Prions, oncogenic DNAVirus, Prions, oncogenic DNA
Storage costInexpensiveModerateModerateModerateExpensiveExpensive

3. Challenges

Current methods in plant biotechnology cannot precisely control the expression level of transgenes in plants in a consistent manner and not every plant species is readily transformed. This means that the amount of pharmaceutical produced may vary in each plant species, or even in different plant parts (i.e., leaves, fruit, and seeds). Levels of expression in subsequent generations may also vary. Given this scenario, it is very difficult to accurately quantify the appropriate dosage of edible vaccines for children and adult patients. Edible vaccines can also trigger immune tolerance after oral administration. Lastly, most of the ingested protein will be degraded by digestive processes. Collectively, these disadvantages greatly restrict the clinical use of edible vaccines [30,32].
While the science of PMF is relatively new, microbial and animal cell expression systems have been used for over 30 years, and industry has developed standard and high-throughput purification protocols. In contrast, protocols for the purification of plant-derived pharmaceutical proteins are varied. While plants such as tobacco, maize, and rice, have been used for greenhouse or open-field production of PMF products, each plant species consists of unique sets of proteins and metabolites. As a result, each PMF platform requires its own purification protocol that is tailored to the product being generated and the plant production system [14,15,16,41,42,43]. Factors, such as plant phenolic compounds, plant pathogens, secondary metabolites, pesticides, and fertilizers, increase the difficulty of purifying a PMF product at an industrial level. Field crop-based PMF platforms, such as maize or rice, have pollen contamination issues which raise biosafety concerns as the pollen may contaminate non-transgenic crops that are part of normal agricultural production [44,45,46]. Currently, FDA has a restricted policy for using food crops for the production of recombinant pharmaceutical compounds [47].
ProdiGene, Inc. company (College Station, TX, USA) launched the large-scale production of transgenic maize that produces trypsin. However, the USDA discovered that plant remnants from a previous ProdiGene trial had contaminated a nearby conventional field. ProdiGene was fined $250,000 and charged $3 million to cover the cleanup operation of mishandling the field test. The punitive action forced ProdiGene into bankruptcy. This event represented a significant setback to the commercial use of PMF [48]. In order for PMF to succeed, both standard biosafety procedures and purification protocols need to be established. In this regard, tobacco is a very good candidate for PMF production since it is not a food crop and cannot contaminate other crops by the spread of transgenic pollen [41]. The procedure for gene transfer and expression in tobacco is also simple and well established. Transgenic tobacco plant can be produced in six months and it can produce the protein of interest in both leaves and seeds.

4. PMF Products for Use as Topical Applications and Health Supplements

Some reports have indicated that subcutaneous injections of plant-derived proteins could induce an immunogenic response to plant-specific glycans [49,50,51,52,53]. Topical applications of plant-derived glycoproteins in humans, however, have not resulted in any adverse effects and therefore represent a potential approach for PMF-based products. Topical application of a recombinant plant secretory antibody prevented oral Streptococcal colonization for at least four months in humans [54]. Topical application of soybean-derived monoclonal antibodies (mAbs) readily diffused in human cervical mucus and prevented herpes simplex virus 2 (HSV-2) infection [55]. Tan et al. (2014) [56] expressed human acidic fibroblast growth factor 1 (FGF-1) in the medicinal plant Salvia miltiorrhiza. The product combined the medicinal function of both FGF-1 and bioactive compounds within the medicinal plant. Topical application of extracts obtained from the transgenic medicinal plant significantly stimulated fibroblast cells, promoted blood vessel formation, and accelerated the healing process of burn wounds in mice. This is an example of how PMF can be used to combine the therapeutic function of a recombinant protein and the inherent properties of a medicinal plant. Topical application of a plant extract would significantly reduce the cost of purification and downstream processing. In general, topical application is safer than oral consumption or injection, which would help to address concerns about public safety.
A primary objective of PMF is to reduce the cost of producing novel therapeutic proteins. Using PMF to create a vegetable, seed or fruit health supplement could be a practical alternative to using PMF to develop a processed pharmaceutical drug. Guan et al. (2014) [57,58] expressed lumbrokinase, an anti-thrombotic enzyme from earthworm, in sunflower kernels. Mice and rats that were fed the transgenic kernels exhibited a strong degradation of blood clots [58]. Unlike a vaccine or a therapeutic protein, lumbrokinase has been widely sold and used as a health supplement to dissolve blood clots and maintain healthy cardiovascular function in people. This makes lumbrokinase a good candidate for PMF since, in general, health supplements do not need a medical prescription and have less regulations for commercialization [59].

5. PMF Production Platforms

5.1. Transient Expression Platform

It often takes six months to a year or more to produce transgenic plants. Several generations are required to generate plants that are homozygous for the transgene. Most transformation technologies also result in the gene being inserted randomly into the plant genome. The factor of random insertion, along with the need to identify regulatory elements (promoters) to drive a high-level of foreign gene expression, often results in a low yield of the recombinant protein even in plants that have been stably transformed. The time needed to utilize a standard PMF approach is unsuitable for addressing sudden viral epidemics, such as an outbreak of Ebola, severe acute respiratory syndrome (SARS), or MERS-CoV. Transient expression systems can be used as an alternative approach to produce recombinant protein within three to five days [60,61,62,63] (see Figure 2).
Various viral vectors have been developed for small- or medium-scale PMF production. For example, Mason et al. (2010) [64] developed a highly efficient, bean yellow dwarf virus (BeYDV) based single-vector DNA replicon system, which incorporated multiple DNA replicon cassettes. They were able to produce 0.5 mg of antibody per gram leaf (fresh weight) in tobacco leaves within four days following infiltration. Mapp Biopharmaceutical Inc., using similar methodology, transiently expressed the humanized antibodies, MB-003 and ZMab, in tobacco leaves. MB-003 and ZMab were later combined and designated as ZMapp. The use of these antibodies as a pharmaceutical drug was able to cure 100% of Ebola infected rhesus macaques primates [65]. Agrobacterium infiltration of leaves for transient expression is very lab intensive and is the primary reason that sufficient supplies of the Ebola vaccine are not available. In September 2014, the U.S Department of Health and Human Service (HHS) provided a grant of $42.2 million to Mapp Biopharmaceutical Inc. for developing a method for large-scale production of ZMapp. With further optimization of the transient expression system, large-scale production in a short time period (one week) may become feasible [66].
Figure 2. A plant-based transient expression system. Bean yellow dwarf virus (BeYDV) based single-vector DNA replicon system, pBY030.2R, is used to transiently express green fluorescent protein (GFP) in tobacco leaves. (A) Infiltration of Agrobacterium carrying the GFP transgene (Left); and transient expression of GFP (Right). Infiltrated leave examined with a UV lamp at four days post infiltration; (B) Diagram of the pBY030.2R vector (kindly provided by Hugh Mason, Arizona State University, Tempe, AZ, USA) used in this study. 35S/TEV 5′, CaMV 35S promoter with tobacco etch virus 5′ UTR; VSP 3′, soybean vspB gene 3′ element; npt II, expression cassette encoding nptII gene for kanamycin resistance; LIR, long intergenic region of BeYDV genome; SIR (yellow oval), short intergenic region of BeYDV genome; C1/C2, BeYDV ORFs C1 and C2, encoding Rep and RepA; LB and RB, the left and right borders of the T-DNA region.
Figure 2. A plant-based transient expression system. Bean yellow dwarf virus (BeYDV) based single-vector DNA replicon system, pBY030.2R, is used to transiently express green fluorescent protein (GFP) in tobacco leaves. (A) Infiltration of Agrobacterium carrying the GFP transgene (Left); and transient expression of GFP (Right). Infiltrated leave examined with a UV lamp at four days post infiltration; (B) Diagram of the pBY030.2R vector (kindly provided by Hugh Mason, Arizona State University, Tempe, AZ, USA) used in this study. 35S/TEV 5′, CaMV 35S promoter with tobacco etch virus 5′ UTR; VSP 3′, soybean vspB gene 3′ element; npt II, expression cassette encoding nptII gene for kanamycin resistance; LIR, long intergenic region of BeYDV genome; SIR (yellow oval), short intergenic region of BeYDV genome; C1/C2, BeYDV ORFs C1 and C2, encoding Rep and RepA; LB and RB, the left and right borders of the T-DNA region.
Ijms 16 26122 g002

5.2. Bioreactor-Based Platforms

Plant-Cell-Culture System

Plant-cell-culture based bioreactors currently show more promise than traditional PMF using whole plants to produce pharmaceuticals [67,68,69]. Similar to microbial or mammalian cell bioreactors, plant cells are cultured in a sealed, sterilized container system without human pathogens or soil contamination. Biosafety concerns associated with the unintentional distribution of pollen and cross-fertilization are also eliminated. Cultured plant cells require only simple nutrients to grow, so the operational cost is much less expensive than mammalian or microbial bioreactors. Downstream purification and processing of the recombinant protein is less complicated in the absence of complex plant fibers and an array of secondary metabolites, which significantly reduces production costs. As previously noted, the first FDA approved PMF-based pharmaceutical, taliglucerase alfa, used to treat Guacher’s disease, was produced in carrot cell suspension cultures (Table 1 and Table 2) [17]. Since Gaucher’s disease is a very rare disease, treatment of this disease with an orphan drug is very costly ($200,000 US annually per patient for life). Using a carrot cell production system, however, reduces the cost to $150,000/patient/year. More than 20 recombinant proteins have been produced from plant cell culture systems [41]. The tobacco strains, BY-2 and NT-1, are the most popular plant cell-culture based strains used as bioreactors in PMF. The recombinant protein can be expressed to be secreted into the culture medium to simplify the downstream purification process. The pore size in plant cell walls, however, may prevent some foreign proteins from being secreted depending on their size and folded architecture [67]. Proteolytic activity in cultured cells may also result in a low yield of antibodies. Magy et al. [68] demonstrated that the proteolytic profile is host species specific. They tested the combination of the isotype, culture conditions, and host species and found that the best combination resulted in 10-fold differences in the expression level. More than 30 mg/L intact antibody was produced in optimum conditions. A yield of 20 mg/L of the human monoclonal antibody M12 was produced in tobacco-BY-2 cell cultures in a 200 L bioreactor [69]. A commercial, cost-effective plant cell culture platform, ProCellEx™ (Protalix Biotherapeutics, Karmiel, Israel) has been developed that significantly reduces costs for industrial scale recombinant protein production [70].

5.3. Moss Culture

Currently, the use of moss, a non-seed plant, is being investigated as a candidate for the production of pharmaceutical proteins in bioreactors [71,72,73]. The ability of moss cells to photosynthesize in culture significantly reduces the cost of culture nutrients. As in yeast and plant cell suspension cultures, recombinant proteins can be designed to be secreted into the culture medium in moss cultures, which facilitates downstream processing and purification of the recombinant protein. Using genetic manipulation, moss cells can also produce a humanized form of a glycosylated protein, lewis Y-specific mAb MB314 [72], which reduces concerns, as noted below, about plant-specific glycosylation. Some recombinant therapeutic proteins, such as Epidermal Growth Factor [74], α-galactosidase [74], α-amylase [75], a glyco-optimized version of the antibody IGN311 [76], a multi-epitope fusion protein from the human immunodeficiency virus [77], etc. have all been produced in moss cultures. Cultures of the moss, Physcomitrella patens (P. patens), are the most commonly used plant material within bioreactors to enable protein production. A German biopharmaceutical company, Greenovation Biotech GmbH, has developed a P. patens-based platform (Bryo-Technology) for large-scale, high quality, recombinant protein production. Examples include Moss-GAA for Pompe Disease, Moss-GBA for Gaucher’s Disease, and Moss-AGAL for Fabry Disease. Moss-AGAL has completed preclinical trials and is entering Phase I testing (Table 1).

5.4. Algal Bioreactors

Microalgae cultures have been used for biofuel and foreign protein production for many years [78,79,80]. Microalgae have a very simple structure, and can be unicellular, colonial, or filamentous. Algae can produce large amount of biomass within a very short period due to their short life cycle. The downstream purification of recombinant proteins in algae is similar to yeast and bacterial systems, and is therefore generally less expensive than whole plant production systems. However, recombinant proteins produced from algae do not undergo certain post translational modifications, and as a result, may not be suitable for the production of some glycoproteins. For example, algae may not be able to produce human forms of glycosylated proteins due to a lack of the proper enzymatic machinery [81]. However, a variety of therapeutic and diagnostic recombinant proteins, including vaccines, enzymes, and antibodies, have been produced in algal systems [82,83,84]. In some cases, however, foreign genes are only expressed transiently in algae [85,86,87]. Efficient and stable expression of foreign genes in algae is greatly improved by the use of strong promoters, proper codon usage, intron integration, and specific transformation methods [88]. An optimized microalgae production system has been developed by a USA-based algae bioreactor company, PhycoBiologics [24]. Recombinant protein yields up to 20% of total soluble protein have been obtained, which makes the algal platform a promising approach for the production of commercial pharmaceuticals [24].

5.5. Seed-Based Platforms

Protein stability is also an important issue in the storage of harvested PMF-based recombinant products. Currently, most pharmaceutical proteins are synthesized in leafy crops for optimum biomass. Leaf proteins, however, are subject to rapid proteolytic degradation after they are harvested [41]. Long-term storage of leaf material is also very challenging. Overexpression of foreign proteins in leaf cells may also result in necrosis and subsequent cell cell death [89]. Our own prelimary studies demonstrated that transient expression of various blood clot-dissolving serine proteinases, such as vampire bat plasminogen activator (DSPAα1), nattokinase, and lumbrokinase, in leaves resulted in leaf necrosis four days after infiltration (Figure 3). When these proteins were targeted to in seeds, however, cell necrosis was not observed and the purified proteins exhibited the ability to dissolve fibrin and blood clots (unpublished data). Therefore, targeting the production of PMF-based products to seeds is becoming an attractive alternative [8,57,58,90,91,92,93,94].
Figure 3. Production of some foreign proteins in leaf cells causes necrosis of plant leaf tissues: 1: GFP; 2: Agrobacterium tumefaciens only; 3: Nattokinase; 4: Lumbrokinase; and 5: DSPAα1 (vampire bat plasminogen activator α1). Picture shows leaf necrosis under visible (A); and UV light (B) four days after infilration using a transient expression platform.
Figure 3. Production of some foreign proteins in leaf cells causes necrosis of plant leaf tissues: 1: GFP; 2: Agrobacterium tumefaciens only; 3: Nattokinase; 4: Lumbrokinase; and 5: DSPAα1 (vampire bat plasminogen activator α1). Picture shows leaf necrosis under visible (A); and UV light (B) four days after infilration using a transient expression platform.
Ijms 16 26122 g003
Seed-based systems for PMF have been developed in various plant species, including Arabidopsis [90,92], tobacco [91], rice [93], and corn [94]. Recombinant proteins targeted to seeds have been reported to accumulate to very high levels. The use of a seed specific, Phaseolus vulgaris regulatory sequence to drive transcription of a murine single chain variable fragment (scFV) in Arabidopsis resulted in high yield of recombinant protein (36.5% of total soluble seed protein) [90]. The abundance of human lysozyme in transgenic rice grains was 1% of grain weight [95]. The level of scFV accumulation approached 25% of total protein in tobacco seeds when scFV was fused with elastin-like polypeptides [96].
Different subcellular compartments have been targeted for recombinant protein in order to increase protein stability in seeds. The ER (endoplasmic reticulum) compartment in plant cells has been demonstrated to contain few proteases and therefore represents a relatively protective environment. Retention of proteins in the ER therefore increases protein stability and yield due to the lack of protein degradation. KDEL, an ER signal peptide, was used to target the deposition of a recombinant protein to the ER [91,97]. Recombinant protein targeted to seeds also allows long-term storage (up to three years) at room temperature without a detectable loss in activity [8].
Targeting of PMF-based products to seeds allows for long-term protein stability, as well as easy harvesting, storage, and transportation. Relative to leaves, seeds contain fewer native proteins and less phenolic compounds and secondary metabolites. Seeds are easy to surface wash and sterilize which also facilitates commercial production. Collectively, the advantages of producing recombinant proteins in seeds make this platform a cost-effective platform for PMF-based products [8,98].

6. Humanized Glycosylation in Plants for “Glycan-Better” Products

Greater than 50% of human proteins are glycosylated. One third of all approved pharmaceuticals are glycoproteins [41]. Plants present an advantage for the production of recombinant proteins due to their capability of performing a variety of post-translational modifications, including glycosylation and lipid addition. Plants and animals share a similar early stage glycosylation pathway before nascent N-glycan reaches the Golgi apparatus. This pathway produces β-(1,4)-linked galactose and sialic acid in animals and N-glycan (core β-(1,2) xylose and core α-(1,3)) fucose moieties in plant. Glycosylation of native plant proteins is essential for their proper function during plant growth and development [99,100,101].
Plant-specific, hyperglycosylated proteins, however, may be immunogenic in humans. Immunization of mice and rats with horseradish peroxidase elicited the production of antibodies (Abs) specific for plant glycans [52]. Immunization of rabbits with a plant-derived, human monoclonal antibody resulted in a strong immune response to a plant specific glycan [49]. A human sera test also detected antibodies to plant glycans. The anti-plant glycan immune response is highly undesirable and could prevent regulatory approval of a glycosylated PMF when the recombinant protein is intended to be administered by injection [11]. Few human trials have investigated whether or not PMF-based recombinant proteins can elicit an immunogenic response in human patients, although it has been estimated that at least 20% of patients would be allergic to plant specific N-glycan [50]. Even though no clinical trials have revealed an adverse effect from an immune response to plant glycans, the subject is still a source of debate and has hampered the development of PMF-based pharmaceuticals [11,102].
Researchers have addressed concerns about plant-specific glycosylation by altering the pathway that plant cells use to process the recombinant protein. Recombinant proteins have been targeted to the endoplasmic reticulum (ER) where non-immunogenic, high-Man-type N-Glycans are produced [103]. Other studies have tried to prevent the production of plant glycan moieties using a knockout [104] or by silencing α-(1,3) FucT and β-(1,2) XylT with RNAi or an antisense approach [79,105,106]. Strasser et al. (2004) [104] produced a triple knockout in Arabidopsis, resulting in the absence of plant-specific glycans, in order to produce recombinant protein with humanized glycan structures. A recombinant human antibody fragment and an active enzyme were successfully produced with a controlled glycosylation pattern using this triple knockout Arabidopsis mutant [99]. RNAi lines of Lemna [79], alfalfa [105], and tobacco [106] have been developed that down regulate β-(1,2) XylT and α-(1,3) FucT activity. All of these RNAi lines were capable of producing human proteins without the addition of plant-specific glycans.
Efforts to optimize the plant glycosylation pathway have improved the therapeutic safety of PMF-derived recombinant proteins and reduced concerns about plant-specific glycan immunogenicity [103]. Protalix Biotherapeutics has produced a “glycan-better” taliglucerase alfa (ELELYSOTM) to treat the rare genetic disorder, Gaucher’s disease. The enzyme is targeted to the vacuole of carrot cells. Unlike the equivalent product produced in CHO cells, which express a recombinant protein with a terminal sialic residue that needs to be removed by an exoglycosidase to expose the terminal mannose moiety, the recombinant enzyme produced in a plant-based system already exhibited terminal mannose residues capable of specifically binding to the receptor on a microphage. The plant derived recombinant protein does not need an enzyme to expose mannose residues, which significantly lowers the cost and complexity of downstream processing; thus reducing the costs of production and therapy. Another example is Lemna (duckweed)-derived mAbs (Biolex/Synthon, Durham, NC, USA). RNAi technology was used to reduce the level of enzymes involved with plant core β-(1,2) xylose and core α-(1,3) fucose synthesis The recombinant mAbs produced in the duckweed system contains a single major N-glycan that has a 20-fold better antibody-dependent cell-mediated cytotoxicity and a 10-fold higher cell receptor binding activity than mAbs produced in CHO cells [79].

7. Downstream Processing

Extraction and purification of PMF-derived pharmaceutical proteins can be complex and costly from an industrial perspective. It has been estimated that purification and downstream processing represents 80% to 90% of the cost of producing PMF-derived pharmaceuticals [42]. For each platform, a specific recovery and purification protocol has to be optimized. Numerous protein recovery and purification processes have been developed on a case-by-case basis [107]. For example, Kentucky Bioprocessing Inc. (Owensboro, KY, USA) has developed a platform of protein expression, production, and processing in transgenic tobacco that conforms to Current Good Manufacturing Practices (cGMP) [23]. Healthgen Biotechnology Corp. (Wuhan, China) has developed an rice seed- based platform, OryzExpress, for producing a variety of products, such as recombinant human albumin, antitrypsin, protease inhibitor, IGF-1, etc. [29]. Plant substances, such as waxes, phenolic compounds, pigments, lignin, and endogenous proteases, also create problems in downstream processing. For instance, phenolic oxidation can result in protein aggregation and precipitation, or endogenous proteases can cause proteolysis [88]. The overall strategy used for downstream processing has to be economically competitive, robust, and compliant with cGMP [108]. In 2015, Caliber Biotherapeutics [109] built a plant-based manufacturing facility that has capacity to process over 3500 kg of tobacco (Nicotiana benthamianai) biomass per week. A transient expression approach is used to produce “biobetter” monoclonal antibodies (mAb) and anti-viral mAb. The downstream processes in this facility include an automated system for the production of various buffers used for separation, high-capacity chromatography, and formulation (cryostorage). Yields of the recombinant protein are in the range of 62%–68% of total protein and the purity of the final product is 95%–98% [110]. The costs of producing, purifying, and formulating the PMF products has been significantly reduced. For example, plant-derived vaccines for the flu cost $0.10 to $0.12 per 50-μg dose [110].

8. Conclusions

Plants have the potential to rapidly produce recombinant proteins on a large scale at a relatively low cost compared to other production systems. PMF-based production of pharmaceuticals, topical compounds, and nutritional supplements is feasible, however, concerns about biosafety, human health (allergenic response to plant-specific glycans), and other factors need to be adequately addressed. Downstream processing and purification of PMF products is currently tedious and costly. Systems need to be developed that simplify the purification process in order to make the production of industrial quantities of PMF-based products feasible and cost effective. The right candidate genes, a strong commercial need, and a good production system will build a bridge between basic research on PMF and its commercial application.


This work was supported by the National Institute of General Medical Sciences of the National Institutes of Health (8P20GM103447).

Author Contributions

Jian Yao conceived the study and drafted the manuscript. Yunqi Weng analyzed data and helped write the paper. Alexia Dickey participated in experiments and preparation of figures. Kevin Yueju Wang coordinated and helped write the manuscript. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declare no conflict of interest.


Plant Molecular Farming (PMF), Single chain variable fragment (scFV), Endoplasmic reticulum (ER), Bean yellow dwarf virus (BeYDV).


  1. Arntzen, C. Plant-made pharmaceuticals: From “Edible Vaccines” to Ebola therapeutics. Plant Biotechnol. 2015, 13, 1013–1016. [Google Scholar] [CrossRef] [PubMed]
  2. Mapp Biopharmaceutical, Inc. Home Page. Available online: (accessed on 27 November 2015).
  3. World Health organization Middle East respiratory syndrome coronavirus (MERS-CoV) Updates Home Page. Available online: (accessed on 27 November 2015).
  4. Planet Biotechnology Inc. Home Page. Available online: (accessed on 27 November 2015).
  5. Barta, A.; Sommengruber, K.; Thompson, D.; Hartmuth, K.; Matzke, M.; Matzke, A. The expression of a napoline synthase human growth hormone chimeric gene in transformed tobacco and sunflower callus tissue. Plant Mol. Biol. 1986, 6, 347–357. [Google Scholar] [CrossRef] [PubMed]
  6. Mason, H.S.; Lam, D.M.; Arntzen, C.J. Expression of hepatitis B surface antigen in transgenic plants. Proc. Natl. Acad. Sci. USA 1992, 89, 11745–11749. [Google Scholar] [CrossRef] [PubMed]
  7. Paul, M.; Ma, J.K. Plant-made pharmaceuticals: Leading products and production platforms. Biotechnol. Appl. Biochem. 2011, 58, 58–67. [Google Scholar] [CrossRef] [PubMed]
  8. Boothe, J.; Nykiforuk, C.; Shen, Y.; Zaplachinski, S.; Szarka, S.; Kuhlman, P.; Murray, E.; Morck, D.; Moloney, M.M. Seed-based expression systems for plant molecular farming. Plant Biotechnol. J. 2010, 8, 588–606. [Google Scholar] [CrossRef] [PubMed]
  9. Sack, M.; Rademacher, T.; Spiegel, H.; Boes, A.; Hellwig, S.; Drossard, J.; Stoger, E.; Fischer, R. From gene to harvest: Insights into upstream process development for the GMP production of a monoclonal antibody in transgenic tobacco plants. Plant Biotechnol. J. 2015. [Google Scholar] [CrossRef] [PubMed]
  10. Abiri, R.; Valdiani, A.; Maziah, M.; Shaharuddin, N.A.; Sahebi, M.; Yusof, Z.Y.; Atabaki, N.; Talei, D.A. Critical review of the concept of transgenic plants: Insights into pharmaceutical biotechnology and molecular farming. Curr. Issues Mol. Biol. 2015, 18, 21–42. [Google Scholar] [PubMed]
  11. Gomord, V.; Fitchette, A.C.; Menu-Bouaouiche, L.; Saint-Jore-Dupas, C.; Plasson, C.; Michaud, D.; Faye, L. Plant-specific glycosylation patterns in the context of therapeutic protein production. Plant Biotechnol. J. 2010, 8, 564–587. [Google Scholar] [CrossRef] [PubMed]
  12. Ullrich, K.K.; Hiss, M.; Rensing, S.A. Means to optimize protein expression in transgenic plants. Curr. Opin. Biotechnol. 2015, 32, 61–67. [Google Scholar] [CrossRef] [PubMed]
  13. Kristina, K.L.; Zeng, W.; Heazlewood, J.L.; Bacic, A. Characterization of protein N-glycosylation by tandem mass spectrometry using complementary fragmentation techniques. Front. Plant Sci. 2015, 6. [Google Scholar] [CrossRef]
  14. Buyel, J.F.; Fischer, R. A juice extractor can simplify the downstream processing of plant-derived biopharmaceutical proteins compared to blade-based homogenizers. Process Biochem. 2014, 50, 859–866. [Google Scholar] [CrossRef]
  15. Buyel, J.F.; Twyman, R.M.; Fischer, R. Extraction and downstream processing of plant-derived recombinant proteins. Biotechnol. Adv. 2015, 33, 902–913. [Google Scholar] [CrossRef] [PubMed]
  16. Fischer, R.; Vasilev, N.; Twyman, R.M.; Schillberg, S. High-value products from plants: The challenges of process optimization. Curr. Opin. Biotechnol. 2015, 32, 56–62. [Google Scholar] [CrossRef] [PubMed]
  17. Fox, J.L. First plant-made biologic approved. Nat. Biotechnol. 2012, 30. [Google Scholar] [CrossRef]
  18. U.S. National Institutes of Health Clinical Trial Home Page. Available online: (accessed on 27 November 2015).
  19. Protealix Biotherapeutics Home Page. Available online: (accessed on 27 November 2015).
  20. Icon Genetics GmbH Home Page. Available online: (accessed on 27 November 2015).
  21. Ventria Biosciences Home Page. Available online: (accessed on 27 November 2015).
  22. Greenovation Biotech GmbH Home Page. Available online: (accessed on 27 November 2015).
  23. Kentucky BioProcessing Home Page. Available online: (accessed on 27 November 2015).
  24. PhycoBiologics Inc., Home Page. Available online: (accessed on 27 November 2015).
  25. Medicago Home Page. Available online: (accessed on 27 November 2015).
  26. Synthon Home Page. Available online: (accessed on 27 November 2015).
  27. Fraunhofer IME Home Page. Available online: (accessed on 27 November 2015).
  28. Fraunhofer CMB Home Page. Available online: (accessed on 27 November 2015).
  29. Healthgen Biotechnology Home Page. Available online: (accessed on 27 November 2015).
  30. Walmsley, A.M.; Arntsen, C.J. Plants for delivery of edible vaccines. Curr. Opin. Biotechnol. 2000, 22, 126–129. [Google Scholar] [CrossRef]
  31. Fukuda, K.; Ishida, W.; Harada, Y.; Wakasa, Y.; Takagi, H.; Takaiwa, F.; Fukushima, A. Prevention of allergic conjunctivitis in mice by a rice-based edible vaccine containing modified Japanese cedar pollen allergens. Br. J. Ophthalmol. 2015, 99, 705–709. [Google Scholar] [CrossRef] [PubMed]
  32. Barzegari, A.; Saeedi, N.; Zarredar, H.; Barar, J.; Omidi, Y. The search for a promising cell factory system for production of edible vaccine. Hum. Vaccines Immunother. 2014, 10, 2497–2502. [Google Scholar] [CrossRef] [PubMed]
  33. Lee, G.; Na, Y.J.; Yang, B.G.; Choi, J.P.; Seo, Y.B.; Hong, C.P.; Yun, C.H.; Kim, D.H.; Sohn, E.J.; Kim, J.H.; et al. Oral immunization of haemaggulutinin H5 expressed in plant endoplasmic reticulum with adjuvant saponin protects mice against highly pathogenic avian influenza A virus infection. Plant Biotechnol. J. 2015, 13, 62–72. [Google Scholar] [CrossRef] [PubMed]
  34. Rosales-Mendoza, S.; Salazar-González, J.A. Immunological aspects of using plant cells as delivery vehicles for oral vaccines. Expert Rev. Vaccines 2014, 13, 737–749. [Google Scholar] [CrossRef] [PubMed]
  35. Aboul-Ata, A.A.; Vitti, A.; Nuzzaci, M.; El-Attar, A.K.; Piazzolla, G.; Tortorella, C.; Harandi, A.M.; Olson, O.; Wright, S.A.; Piazzolla, P. Plant-based vaccines: Novel and low-cost possible route for Mediterranean innovative vaccination strategies. Adv. Virus Res. 2014, 89, 1–37. [Google Scholar] [PubMed]
  36. Kong, Q.; Richter, L.; Yang, Y.F.; Arntzen, C.J.; Mason, H.S.; Thanavala, Y. Oral immunization with hepatitis B surface antigen expressed in transgenic plants. Proc. Natl. Acad. Sci. USA 2001, 98, 11539–11544. [Google Scholar] [CrossRef] [PubMed]
  37. Thanavala, Y.; Mahoney, M.; Pal, S.; Scott, A.; Richter, L.; Natarajan, N.; Goodwin, P.; Arntzen, C.J.; Mason, H.S. Immunogenicity in humans of an edible vaccine for hepatitis B. Proc. Natl. Acad. Sci. USA 2005, 102, 3378–3382. [Google Scholar] [CrossRef] [PubMed]
  38. Hefferon, K. Clinical trials fuel the promise of plant-derived vaccines. Am. J. Clin. Med. 2010, 7, 30–37. [Google Scholar]
  39. Antibodies-online Inc. Home Page. Available online: (accessed on 27 November 2015).
  40. PromoKine Home Page. Available online: (accessed on 27 November 2015).
  41. Spök, A.; Karner, S. Plant Molecular Farming, Opportunities and Challenges; JRC Technical Report EUR 23383 EN; Office for Official Publications of the European Communities: Kopstal, Luxembourg, 2008. [Google Scholar]
  42. Sabalza, M.; Christou, P.; Capell, T. Recombinant plant-derived pharmaceutical proteins: Current technical and economic bottlenecks. Biotechnol. Lett. 2014, 36, 2367–2379. [Google Scholar] [CrossRef] [PubMed]
  43. Lallemand, J.; Bouché, F.; Desiron, C.; Stautemas, J.; de LemosEsteves, F.; Périlleux, C.; Tocquin, P. Extracellular peptidase hunting for improvement of protein production in plant cells and roots. Front. Plant Sci. 2015, 6. [Google Scholar] [CrossRef] [PubMed][Green Version]
  44. Breyer, D.; Goossens, M.; Herman, P.; Sneyers, M. Biosafety considerations associated with molecular farming in genetically modified plants. J. Med. Plant Res. 2009, 3, 825–838. [Google Scholar]
  45. Sparrow, P.; Broer, I.; Hood, E.E.; Eversole, K.; Hartung, F.; Schiemann, J. Risk assessment and regulation of molecular farming—A comparison between Europe and US. Curr. Pharm. Des. 2013, 19, 5513–5530. [Google Scholar] [CrossRef] [PubMed]
  46. MacDonald, J.; Doshi, K.; Dussault, M.; Hall, J.C.; Holbrook, L.; Jones, G.; Kaldis, A.; Klima, C.L.; Macdonald, P.; McAllister, T.; et al. Bringing plant-based veterinary vaccines to market: Managing regulatory and commercial hurdles. Biotechnol. Adv. 2015. [Google Scholar] [CrossRef] [PubMed]
  47. FDA guidance for industry: Drugs, biologics, and medical devices derived from bioengineered plants for use in humans and animals (draft guidance). FDA website. Available online: Http:// (accessed on 27 November 2015).
  48. Strauss, D.M. Liability for genetically modified food: Are GMOs a tort waiting to happen? SciTech Lawyer 2012, 9, 8–13. [Google Scholar]
  49. Jin, C.; Altmann, F.; Strasser, R.; Mach, L.; Schähs, M.; Kunert, R.; Rademacher, T.; Glössl, J.; Steinkellner, H. A plant-derived human monoclonal antibody induces an anti-carbohydrate immune response in rabbits. Glycobiology 2008, 18, 235–241. [Google Scholar] [CrossRef] [PubMed]
  50. Mari, A. IgE to cross-reactive carbohydrate determinants: Analysis of the distribution and appraisal of the in vivo and in vitro reactivity. Int. Arch. Allergy Immunol. 2002, 129, 286–295. [Google Scholar] [CrossRef] [PubMed]
  51. Costa, A.R.; Rodrigues, M.E.; Henriques, M.; Oliveira, R.; Azeredo, J. Glycosylation: Impact, control and improvement during therapeutic protein production. Crit. Rev. Biotechnol. 2014, 34, 281–299. [Google Scholar] [CrossRef] [PubMed]
  52. Bardor, M.; Faveeuw, C.; Fitchette, A.C.; Gilbert, D.; Galas, L.; Trottein, F.; Faye, L.; Lerouge, P. Immunoreactivity in mammals of two typical plant glyco-epitopes, core alpha(1,3)-fucose and core xylose. Glycobiology 2003, 13, 427–434. [Google Scholar] [CrossRef] [PubMed]
  53. Castilho, A.; Steinkellner, H. Glyco-engineering in plants to produce human-like N-glycan structures. Biotechnol. J. 2012, 7, 1088–1098. [Google Scholar] [CrossRef] [PubMed]
  54. Ma, J.K.C.; Hikmat, B.Y.; Wycoff, K.; Vine, N.D.; Chargelegue, D.; Yu, L.; Hein, M.B.; Lherner, T. Characterization of a recombinant plant monoclonal secretory antibody and preventive immunotherapy in humans. Nat. Med. 1998, 4, 601–606. [Google Scholar] [CrossRef] [PubMed]
  55. Zeitlin, L.; Olmsted, S.S.; Moench, T.C.; Co, M.S.; Martinell, B.J.; Paradkar, V.M.; Russell, D.R.; Queen, C.; Cone, R.A.; Whaley, K. A humanized monoclonal antibody produced in transgenic plants for immunoprotection of the vagina against genital herpes. Nat. Biotechnol. 1998, 16, 1361–1364. [Google Scholar] [PubMed]
  56. Tan, Y.; Wang, K.Y.; Wang, N.; Li, G.; Liu, D. Ectopic expression of human acidic fibroblast growth factor 1 in the medicinal plant, Salvia miltiorrhiza, accelerates the healing of burn wounds. BMC Biotechnol. 2014, 14. [Google Scholar] [CrossRef] [PubMed]
  57. Guan, C.; Ji, J.; Jin, C.; Wang, G.; Li, X.; Guan, W. Expression of cholera toxin B subunit-lumbrokinase in edible sunflower seeds-the use of transmucosal carrier to enhance its fusion protein’s effect on protection of rats and mice against thrombosis. Biotechnol. Prog. 2014, 30, 1029–1039. [Google Scholar] [CrossRef] [PubMed]
  58. Guan, C.; Du, X.; Wang, G.; Ji, J.; Jin, C.; Li, X. Expression of biologically active anti-thrombosis protein lumbrokinase in edible sunflower seed kernel. J. Plant. Biochem. Biotechnol. 2014, 23, 257–265. [Google Scholar] [CrossRef]
  59. Wang, K.; Tull, L.; Cooper, E.; Wang, N.; Liu, D. Recombinant protein production of earthworm lumbrokinase for potential antithrombotic application. Evid. Based Complement. Altern. Med. 2013, 783971. [Google Scholar] [CrossRef] [PubMed]
  60. Andrews, L.B.; Curtis, W.R. Comparison of transient protein expression in tobacco leaves and plant suspension culture. Biotechnol. Prog. 2005, 21, 946–952. [Google Scholar] [CrossRef] [PubMed]
  61. Sainsbury, F.; Lomonossoff, G.P. Transient expressions of synthetic biology in plants. Curr. Opin. Plant Biol. 2014, 19, 1–7. [Google Scholar] [CrossRef] [PubMed]
  62. Peyret, H.; Lomonossoff, G.P. When plant virology met Agrobacterium: The rise of the deconstructed clones. Plant Biotechnol. J. 2015, 13, 1121–1135. [Google Scholar] [CrossRef] [PubMed]
  63. Catrice, E.V.; Sainsbury, F. Assembly and purification of polyomavirus-like particles from plants. Mol. Biotechnol. 2015, 57, 904–913. [Google Scholar] [CrossRef] [PubMed]
  64. Huang, Z.; Phoolcharoen, W.; Lai, H.; Piensook, K.; Cardineau, G.; Zeitlin, L.; Whaley, K.J.; Arntzen, C.J.; Mason, H.S.; Chen, Q. High-level rapid production of full-size monoclonal antibodies in plants by a single-vector DNA replicon system. Biotechnol. Bioeng. 2010, 106, 9–17. [Google Scholar] [CrossRef] [PubMed]
  65. Qiu, X.; Wong, G.; Audet, J.; Bello, A.; Fernando, L.; Alimonti, J.B.; Fausther-Bovendo, H.; Wei, H.; Aviles, J.; Hiatt, E.; et al. Reversion of advanced Ebola virus disease in nonhuman primates with ZMapp. Nature 2014, 514, 47–53. [Google Scholar] [CrossRef] [PubMed]
  66. U.S. Department of Health & Human Service: Partnership advances experimental Ebola drug. Available online: (accessed on 27 November 2015).
  67. Schillberg, S.; Raven, N.; Fischer, R.; Twyman, R.M.; Schiermeyer, A. Molecular farming of pharmaceutical proteins using plant suspension cell and tissue cultures. Curr. Pharm. 2013, 19, 5531–5542. [Google Scholar] [CrossRef]
  68. Magy, B.; Tollet, J.; Laterre, R.; Boutry, M.; Navarre, C. Accumulation of secreted antibodies in plant cell cultures varies according to the isotype, host species and culture conditions. Plant Biotechnol. J. 2014, 12, 457–467. [Google Scholar] [CrossRef] [PubMed]
  69. Raven, N.; Rasche, S.; Kuehn, C.; Anderlei, T.; Klöckner, W.; Schuster, F.; Henquet, M.; Bosch, D.; Büchs, J.; Fischer, R.; et al. Scaled-up manufacturing of recombinant antibodies produced by plant cells in a 200-L orbitally-shaken disposable bioreactor. Biotechnol. Bioeng. 2015, 112, 308–321. [Google Scholar] [CrossRef] [PubMed]
  70. Tekoah, Y.; Shulman, A.; Kizhner, T.; Ruderfer, I.; Fux, L.; Nataf, Y.; Bartfeld, D.; Ariel, T.; Gingis-Velitski, S.; Hanania, U.; et al. Large-scale production of pharmaceutical proteins in plant cell culture-the protalix experience. Plant Biotechnol. J. 2015, 13, 1199–1208. [Google Scholar] [CrossRef] [PubMed]
  71. Huang, T.K.; McDonald, K.A. Bioreactor systems for in vitro production of foreign proteins using plant cell cultures. Biotechnol. Adv. 2012, 30, 398–409. [Google Scholar] [CrossRef] [PubMed]
  72. Kircheis, R.; Halanek, N.; Koller, I.; Jost, W.; Schuster, M.; Gorr, G.; Hajszan, K.; Nechansky, A. Correlation of ADCC activity with cytokine release induced by the stably expressed, glyco-engineered humanized Lewis Y-specific monoclonal antibody MB314. MABS 2012, 4, 532–541. [Google Scholar] [CrossRef] [PubMed]
  73. Reski, R.; Parsons, J.; Decker, E.L. Moss-made pharmaceuticals: From bench to bedside. Plant Biotechnol. J. 2015, 13, 1191–1198. [Google Scholar] [CrossRef] [PubMed]
  74. Niederkrüger, H.; Dabrowska-Schlepp, P.; Schaaf, A. Suspension culture of plant cells under phototrophic conditions. In Industrial Scale Suspension Culture of Living Cells; Meyer, H.P., Schmidhalter, D.R., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2014; pp. 259–292. [Google Scholar]
  75. Anterola, A.; Shanle, E.; Perroud, P.F.; Quatrano, R. Production of taxa-4(5), 11(12)-diene by transgenic Physcomitrella patens. Transgenic Res. 2009, 18, 655–660. [Google Scholar] [CrossRef] [PubMed]
  76. Orellana-Escobedo, L.; Rosales-Mendoza, S.; Romero-Maldonado, A.; Parsons, J.; Decker, E.L.; Monreal-Escalante, E.; Moreno-Fierros, L.; Reski, R. An Env-derived multi-epitope HIV chimeric protein produced in the moss Physcomitrella patens is immunogenic in mice. Plant Cell Rep. 2015, 34, 425–433. [Google Scholar] [CrossRef] [PubMed]
  77. Rubio-Infante, N.; Govea-Alonso, D.O.; Alpuche-Solís, Á.G.; García-Hernández, A.L.; Soria-Guerra, R.E.; Paz-Maldonado, L.M.; Ilhuicatzi-Alvarado, D.; Varona-Santos, J.T.; Verdín-Terán, L.; Korban, S.S.; et al. Chloroplast-derived C4V3 polypeptide from the human immunodeficiency virus (HIV) is orally immunogenic in mice. Plant Mol. Biol. 2012, 78, 337–349. [Google Scholar] [CrossRef] [PubMed]
  78. Markou, G.; Nerantzis, E. Microalgae for high-value compounds and biofuels production: A review with focus on cultivation under stress conditions. Biotechnol. Adv. 2013, 31, 1532–1542. [Google Scholar] [CrossRef] [PubMed]
  79. Cox, K.M.; Sterling, J.D.; Regan, J.T.; Gasdaska, J.R.; Frantz, K.K.; Peele, C.G.; Black, A.; Passmore, D.; Moldovan-Loomis, C.; Srinivasan, M.; et al. Glycan optimization of a human monoclonal antibody in the aquatic plant Lemna minor. Nat. Biotechnol. 2006, 24, 1591–1597. [Google Scholar] [CrossRef] [PubMed]
  80. Qin, S.; Lin, H.; Jiang, P. Advances in genetic engineering of marine algae. Biotechnol. Adv. 2012, 30, 1602–1613. [Google Scholar] [CrossRef] [PubMed]
  81. Mathieu-Rivet, E.; Kiefer-Meyer, M.-C.; Vanier, G.; Ovide, C.; Burel, C.; Lerouge, P.; Bardor, M. Protein N-glycosylation in eukaryotic microalgae and its impact on the production of nuclear expressed biopharmaceuticals. Front. Plant Sci. 2014, 5. [Google Scholar] [CrossRef] [PubMed]
  82. Lu, Y.; Oyler, G.A. Green algae as a platform to express therapeutic proteins. Discov. Med. 2009, 8, 28–30. [Google Scholar] [PubMed]
  83. Gong, Y.; Hu, H.; Gao, Y.; Xu, X.; Gao, H. Microalgae as platforms for production of recombinant proteins and valuable compounds: Progress and prospects. J. Ind. Microbiol. Biotechnol. 2011, 38, 1879–1890. [Google Scholar] [CrossRef] [PubMed]
  84. Rasala, B.A.; Mayfield, S.P. The microalga Chlamydomonasreinhardtii as a platform for the production of human protein therapeutics. Bioeng. Bugs 2011, 2, 50–54. [Google Scholar] [CrossRef] [PubMed]
  85. Teng, C.; Qin, S.; Liu, J.; Yu, D.; Liang, C.; Tseng, C. Transient expression of lacZ in bombarded unicellular green alga Haematococcuspluvialis. J. Appl. Phycol. 2002, 14, 497–500. [Google Scholar]
  86. Jarvis, E.E.; Brown, L.M. Transient expression of firefly luciferase in protoplasts of the green alga Chlorella ellipsoidea. Curr. Genet. 1991, 19, 317–321. [Google Scholar] [CrossRef]
  87. Hawkins, R.L.; Nakamura, M. Expression of human growth hormone by the eukaryotic alga, Chlorella. Curr. Microbiol. 1999, 38, 335–341. [Google Scholar] [CrossRef] [PubMed]
  88. Eichler-Stahlberg, A.; Weisheit, W.; Ruecker, O.; Heitzer, M. Strategies to facilitate transgene expression in Chlamydomonas reinhardtii. Planta 2009, 229, 873–883. [Google Scholar] [CrossRef] [PubMed]
  89. Phoolcharoen, W.; Bhoo, S.; Lai, H.; Ma, J.; Arntzen, C.J.; Chen, Q.; Mason, H.S. Expression of an immunogenic Ebola immune complex in Nicotianabenthamiana. Plant Biotechnol. J. 2011, 9, 807–816. [Google Scholar] [CrossRef] [PubMed]
  90. De Jaeger, G.; Scheffer, S.; Jacobs, A.; Zambre, M.; Zobell, O.; Goossens, A.; Depicker, A.; Angenon, G. Boosting heterologous protein production in transgenic dicotyledonous seeds using Phaseolus vulgaris regulatory sequences. Nat. Biotechnol. 2002, 20, 1265–1268. [Google Scholar] [CrossRef] [PubMed]
  91. Lu, Z.; Lee, K.J.; Shao, Y.; Lee, J.H.; So, Y.; Choo, Y.K.; Oh, D.B.; Hwang, K.A.; Oh, S.H.; Han, Y.S.; Ko, K. Expression of GA733-Fc fusion protein as a vaccine candidate for colorectal cancer in transgenic plants. J. Biomed. Biotechnol. 2012, 364240. [Google Scholar] [CrossRef] [PubMed]
  92. Downing, W.L.; Galpin, J.D.; Clemens, S.; Lauzon, S.M.; Samuels, A.L.; Pidkowich, M.S.; Clarke, A.; Kermode, A.R. Synthesis of enzymatically active human α-l-iduronidase in Arabidopsiscgl (complex glycan-deficient) seeds. Plant Biotechnol. J. 2006, 4, 169–181. [Google Scholar] [CrossRef] [PubMed]
  93. Ou, J.; Guo, Z.; Shi, J.; Wang, X.; Liu, J.; Shi, B.; Guo, F.; Zhang, C.; Yang, D. Transgenic rice endosperm as a bioreactor for molecular pharming. Plant Cell Rep. 2014, 33, 585–594. [Google Scholar] [CrossRef] [PubMed]
  94. Zhong, Q.; Gu, Z.; Glatz, C.E. Extraction of recombinant dog gastric lipase from transgenic corn seed. J. Agric. Food Chem. 2006, 54, 8086–8092. [Google Scholar] [CrossRef] [PubMed]
  95. Huang, N. High-level protein expression system uses self-pollinating crops as hosts. BioProcess Int. 2004, 2, 54–59. [Google Scholar]
  96. Scheller, J.; Leps, M.; Conrad, U. Forcing single-chain variable fragment production in tobacco seeds by fusion to elastin-like polypeptides. Plant Biotechnol. J. 2006, 4, 243–249. [Google Scholar] [CrossRef] [PubMed]
  97. Petruccelli, S.; Otegui, M.S.; Lareu, F.; Tran Dinh, O.; Fitchette, A.C.; Circosta, A.; Rumbo, M.; Bardor, M.; Carcamo, R.; Gomord, V.; et al. A KDEL-tagged monoclonal antibody is efficiently retained in the endoplasmic reticulum in leaves, but is both partially secreted and sorted to protein storage vacuoles in seeds. Plant Biotechnol. J. 2006, 4, 511–527. [Google Scholar] [CrossRef] [PubMed]
  98. Khan, I.; Twyman, R.M.; Arcalis, E.; Stoger, E. Using storage organelles for the accumulation and encapsulation of recombinant proteins. Biotechnol. J. 2012, 7, 1099–1108. [Google Scholar] [CrossRef] [PubMed]
  99. Loos, A.; Steinkellner, H. Plant glyco-biotechnology on the way to synthetic biology. Front. Plant Sci. 2014, 5. [Google Scholar] [CrossRef] [PubMed]
  100. Stoger, E.; Fischer, R.; Moloney, M.; Ma, J.K. Plant molecular pharming for the treatment of chronic and infectious diseases. Annu. Rev. Plant Biol. 2014, 65, 743–768. [Google Scholar] [CrossRef] [PubMed]
  101. Moustafa, K.; Makhzoum, A.; Trémouillaux-Guiller, J. Molecular farming on rescue of pharma industry for next generations. Crit. Rev. Biotechnol. 2015, 4, 1–11. [Google Scholar] [CrossRef] [PubMed]
  102. Mari, A.; Ooievaar-de-Heer, P.; Scala, E.; Giani, M.; Pirrotta, L.; Zuidmeer, L.; Bethell, D.; van Ree, R. Evaluation by double-blind placebo-controlled oral challenge of the clinical relevance of IgE antibodies against plant glycans. Allergy 2008, 63, 891–896. [Google Scholar] [CrossRef] [PubMed]
  103. Floss, D.M.; Sack, M.; Arcalis, E.; Stadlmann, J.; Quendler, H.; Rademacher, T.; Stoger, E.; Scheller, J.; Fischer, R.; Conrad, U. Influence of elastin-like peptide fusions on the quantity and quality of a tobacco-derived human immunodeficiency virus-neutralizing antibody. Plant Biotechnol. J. 2009, 7, 899–913. [Google Scholar] [CrossRef] [PubMed]
  104. Strasser, R.; Altmann, F.; Mach, L.; Glössl, J.; Steinkellner, H. Generation of Arabidopsis thaliana plants with complex N-glycans lacking β1,2-linked xylose and core α1,3-linked fucose. FEBS Lett. 2004, 561, 132–136. [Google Scholar] [CrossRef]
  105. Sourrouille, C.; Marquet-Blouin, E.; D’Aoust, M.A.; Kiefer-Meyer, M.C.; Séveno, M.; Pagny-Salehabadi, S.; Bardor, M.; Durambur, G.; Lerouge, P.; Vezina, L.; et al. Down-regulated expression of plant-specific glycoepitopes in alfalfa. Plant Biotechnol. J. 2008, 6, 702–721. [Google Scholar] [CrossRef] [PubMed]
  106. Strasser, R.; Stadlmann, J.; Schähs, M.; Stiegler, G.; Quendler, H.; Mach, L.; Glössl, J.; Weterings, K.; Pabst, M.; Steinkellner, H. Generation of glyco-engineered Nicotianabenthamiana for the production of monoclonal antibodies with a homogeneous human-like N-glycan structure. Plant Biotechnol. J. 2008, 6, 392–402. [Google Scholar] [CrossRef] [PubMed]
  107. Wilken, L.R.; Nikolov, Z.L. Recovery and purification of plant-made recombinant proteins. Biotechnol. Adv. 2012, 30, 419–433. [Google Scholar] [CrossRef] [PubMed]
  108. Chen, Q. Expression and purification of pharmaceutical proteins in plants. Biol. Eng. 2008, 1, 291–321. [Google Scholar] [CrossRef]
  109. Caliber Biotherapeutics Homepage. Available online: (accessed on 27 November 2015).
  110. Holtz, B.R.; Berquist, B.R.; Bennett, L.D.; Kommineni, V.J.M.; Munigunti, R.K.; White, E.L.; Wilkerson, D.C.; Wong, K.I.; Ly, L.H.; Marcel, S. Commercial-scale biotherapeutics manufacturing facility for plant-made pharmaceuticals. Plant Biotechnol. 2015, 13, 1180–1190. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Yao, J.; Weng, Y.; Dickey, A.; Wang, K.Y. Plants as Factories for Human Pharmaceuticals: Applications and Challenges. Int. J. Mol. Sci. 2015, 16, 28549-28565.

AMA Style

Yao J, Weng Y, Dickey A, Wang KY. Plants as Factories for Human Pharmaceuticals: Applications and Challenges. International Journal of Molecular Sciences. 2015; 16(12):28549-28565.

Chicago/Turabian Style

Yao, Jian, Yunqi Weng, Alexia Dickey, and Kevin Yueju Wang. 2015. "Plants as Factories for Human Pharmaceuticals: Applications and Challenges" International Journal of Molecular Sciences 16, no. 12: 28549-28565.

Article Metrics

Back to TopTop