Realising the value of plant molecular pharming to benefit the poor in developing countries and emerging economies

被引:46
作者
Ma, Julian K-C. [1 ]
Christou, Paul [2 ,3 ]
Chikwamba, Rachel [4 ]
Haydon, Hugh [5 ]
Paul, Mathew [1 ]
Ferrer, Merardo Pujol [6 ]
Ramalingam, Sathishkumar [7 ]
Rech, Elibio [8 ]
Rybicki, Edward [9 ]
Wigdorowitz, Andres [10 ]
Yang, Dai-Chang [11 ]
Thangaraj, Harry [1 ]
机构
[1] St Georges Univ London, Div Clin Sci, Hotung Mol Immunol Unit, London, England
[2] Univ Lleida, Dept Prod Vegetal & Ciencia Forestal, Lleida, Spain
[3] ICREA, Barcelona, Spain
[4] CSIR Biosci, Plant Biotechnol Grp, Pretoria, South Africa
[5] Kentucky Bioproc LLC, Owensboro, KY USA
[6] Ctr Genet Engn & Biotechnol, Havana, Cuba
[7] Bharathiar Univ, Dept Biotechnol, Plant Genet Engn Lab, Coimbatore, Tamil Nadu, India
[8] EMBRAPA Genet Resources & Biotechnol, Lab Synthet Biol, Brasilia, DF, Brazil
[9] Univ Cape Town, Dept Mol & Cell Biol, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[10] Inst Nacl Tecnol Agr, Buenos Aires, DF, Argentina
[11] Wuhan Univ, Coll Life Sci, Engn Res Ctr Plant Biotechnol & Germplasm Utiliza, Wuhan 430072, Peoples R China
关键词
molecular pharming; resource-poor; low income; developing countries; regulatory framework; socially responsible licensing; VACCINES;
D O I
10.1111/pbi.12127
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molecular Pharming, the production of recombinant pharmaceuticals through plant biotechnology, has the potential to transform the biologics sector of the pharmaceutical industry. More fascinating however, is how it might be used to improve access to modern medicines, and improve health of the poor in developing countries and emerging economies. Although improving global health through molecular pharming has been discussed for at least two decades, little progress has actually been made. In this manuscript, a four point plan is described to maximise the opportunity for molecular pharming to provide solutions. These are (i) to identify and prioritise important drug targets that are relevant to the poor; (ii) to support research and development partners in low to middle income countries to develop local expertise, transfer technology and build capacity; (iii) to increase collaboration between regulatory bodies to enable national regulatory frameworks to be developed in low to middle income countries; and (iv) to promote intellectual property management approaches that include socially responsible licensing. An existing case study is described to illustrate how this might be achieved.
引用
收藏
页码:1029 / 1033
页数:5
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