2011
DOI: 10.4161/hv.7.3.14456
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Molecular pharming

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Cited by 43 publications
(15 citation statements)
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“…The low production costs, ability of plants to assemble and modify multimeric proteins such as mAbs, and ease of scalability make plants a viable platform for production of mAbs to replace RIG [24, 25]. …”
mentioning
confidence: 99%
“…The low production costs, ability of plants to assemble and modify multimeric proteins such as mAbs, and ease of scalability make plants a viable platform for production of mAbs to replace RIG [24, 25]. …”
mentioning
confidence: 99%
“…[33][34][35][36][37][38][39][40] Several previous studies have shown plant produced HA is effective in mouse and ferret models of influenza challenge, but always require at least two immunizations with adjuvant to stimulate HAI titers or protective immunity. 18,20,41 Disappointing results from a Phase I clinical trial reported only 5-10% seroconversion after 90 µg dosing with an HA vaccine, irrespective of adjuvant co-formulation, 42 or may require 2 doses of alum-adjuvanted vaccine for clinically significant immune protection.…”
Section: Discussionmentioning
confidence: 99%
“…Molecular farming using plants or plant cell lines as a green factory to produce vaccines and biopharmaceuticals has also made considerable progress with commercially released plant-made therapeutic proteins, and a number of vaccines and therapeutic proteins are undergoing clinical trials or are in the pipeline to be approved (Yusibov et al 2011; http://www.genengnews.com/gen-news-highlights/); however, it has encountered the same regulatory constraints as other GM crops. Under the current regulatory requirements, it’s estimated that it takes on average 7-10 million euros to approve a GM crop for cultivation (Paul et al 2011). …”
Section: Regulatory Constraintsmentioning
confidence: 99%