生物
生物技术
功能(生物学)
重组DNA
寄主(生物学)
人类蛋白质
计算生物学
单克隆抗体
细胞
剧目
细胞生物学
生物化学
抗体
遗传学
基因
物理
声学
作者
Christina L. Zuch de Zafra,Valerie Quarmby,Kathleen Francissen,Martin Vanderlaan,Judith X. Zhu-Shimoni
摘要
To manufacture biotechnology products, mammalian or bacterial cells are engineered for the production of recombinant therapeutic human proteins including monoclonal antibodies. Host cells synthesize an entire repertoire of proteins which are essential for their own function and survival. Biotechnology manufacturing processes are designed to produce recombinant therapeutics with a very high degree of purity. While there is typically a low residual level of host cell protein in the final drug product, under some circumstances a host cell protein(s) may copurify with the therapeutic protein and, if it is not detected and removed, it may become an unintended component of the final product. The purpose of this article is to enumerate and discuss factors to be considered in an assessment of risk of residual host cell protein(s) detected and identified in the drug product. The consideration of these factors and their relative ranking will lead to an overall risk assessment that informs decision-making around how to control the levels of host cell proteins.
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