免疫原性
蛋白质聚集
背景(考古学)
计算生物学
生物生产
生化工程
免疫系统
化学
计算机科学
生物
免疫学
生物化学
工程类
古生物学
作者
Ngoc B. Pham,Wilson S. Meng
标识
DOI:10.1016/j.ijpharm.2020.119523
摘要
Recombinant proteins are the mainstay of biopharmaceuticals. A key challenge in the manufacturing and formulation of protein biologic products is the tendency for the active pharmaceutical ingredients to aggregate, resulting in irreversible drug loss, and an increase in immunogenicity risk. While the molecular mechanisms of protein aggregation have been discussed extensively in the literature, knowledge gaps remain in connecting the phenomenon in the context of immunogenicity of biotherapeutics. In this review, we discussed factors that drive aggregation of pharmaceutical recombinant proteins, and highlighted methods of prediction and mitigation that can be deployed through the development stages, from formulation to bioproduction. The purpose is to stimulate new dialogs that would bridge the interface between physical characterizations of protein aggregates in biotherapeutics and the functional attributes of the immune system.
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