MIGAL, Galilee Technology Center, P.O. Box 831, Kiryat Shmona 11016, Israel.
Int Immunopharmacol. 2013 Feb;15(2):254-9. doi: 10.1016/j.intimp.2012.12.012. Epub 2013 Jan 7.
Covalent attachment of PEG (PEGylation) is widely used to improve the pharmaceutical properties of therapeutic proteins. The applicability and safety of this method have been proven by the use of various PEGylated pharmaceutical proteins approved by the Food and Drug Administration (FDA). One of the properties attributed to PEGylation is immunogenicity reduction of the PEGylated protein. In this study, the impact of PEGylation on immunogenicity was tested and compared for two proteins (chicken IgY and horse IgG) in two strains of mice (Balb/c and C57BL/6) for two routes of administration (i.v. and i.m.) and two sizes of PEG (5 kD and 20 kD). The influence of PEG was shown to be inconsistent between the mouse strains and routes of administration, even with the same tested protein. Consequently, immunogenicity reduction by PEGylation cannot be predicted or assumed; it must be tested on an individual case basis.
PEG(聚乙二醇)的共价附着广泛用于改善治疗性蛋白质的药物特性。通过使用食品和药物管理局 (FDA) 批准的各种 PEG 化药物蛋白,已经证明了该方法的适用性和安全性。PEG 化的一个特性是降低 PEG 化蛋白的免疫原性。在这项研究中,对于两种蛋白质(鸡 IgY 和马 IgG),在两种小鼠品系(Balb/c 和 C57BL/6)中,通过两种给药途径(静脉内和肌肉内)和两种 PEG 分子量(5 kD 和 20 kD),测试和比较了 PEG 化对免疫原性的影响。结果表明,PEG 的影响在不同的小鼠品系和给药途径之间不一致,即使使用相同的测试蛋白也是如此。因此,PEG 化的免疫原性降低不能被预测或假设;必须根据具体情况进行测试。