Gomord Véronique, Chamberlain Paul, Jefferis Roy, Faye Loïc
CNRS UMR6037, University of Rouen, IFRMP23, GDR2590, UFR des Sciences, 76 821 Mont Saint Aignan, France.
Trends Biotechnol. 2005 Nov;23(11):559-65. doi: 10.1016/j.tibtech.2005.09.003. Epub 2005 Sep 15.
There are major structural differences between plant and mammalian N-linked glycans, with those from plants being immunogenic in most laboratory mammals and eliciting glycan-specific IgE and IgG antibodies in humans, when delivered parenterally. However, because humans are constantly exposed to plant glycoproteins in the diet, glycosylated plant-made pharmaceuticals (PMPs) should be acceptable for topical and oral administration. To exploit fully the potential that plants offer for the production of therapeutic proteins for parenteral administration, it might be necessary to inhibit plant-specific post-translational modifications to obtain "humanized" non-immunogenic N-glycans on PMPs. The benefits that could accrue are lower manufacturing costs, relative to mammalian cell culture, and a reduced risk of transmission of mammalian pathogens.
植物和哺乳动物的N-连接聚糖在结构上存在重大差异,植物来源的聚糖在大多数实验哺乳动物中具有免疫原性,经肠胃外给药时会在人体内引发聚糖特异性IgE和IgG抗体。然而,由于人类在饮食中经常接触植物糖蛋白,糖基化的植物源药物(PMPs)应该适合局部和口服给药。为了充分利用植物在生产肠胃外给药治疗性蛋白质方面的潜力,可能有必要抑制植物特异性的翻译后修饰,以便在PMPs上获得“人源化”的非免疫原性N-聚糖。相对于哺乳动物细胞培养,这样做可能带来的好处是制造成本降低,以及降低哺乳动物病原体传播的风险。