Technology & Innovation, CMC Science & Intelligence, Merck Serono SpA (an affiliate of Merck KgaA, Darmstadt, Germany), Guidonia Montecelio (Rome), Italy.
Biotech Development Programme, Merck Biopharma (an affiliate of Merck KgaA, Darmstadt, Germany), Aubonne, Switzerland.
Trends Pharmacol Sci. 2021 Nov;42(11):943-956. doi: 10.1016/j.tips.2021.08.004. Epub 2021 Sep 17.
The incorporation of the non-human N-glycolylneuraminic acid (Neu5Gc) in therapeutic recombinant proteins raises clinical concerns due to its immunogenic potential and the high prevalence of pre-existing anti-Neu5Gc antibodies in humans. The scientific literature is ambiguous regarding the actual impact of Neu5Gc-containing biotherapeutics as no severe adverse clinical manifestations were unequivocally attributed to Neu5Gc for currently marketed biotherapeutics. This review discusses structural and functional considerations of Neu5Gc-containing glycans regarding the potential impact on drug clearance, their recognition by pre-existing antibodies, and recent hypotheses regarding the tolerance to low Neu5Gc levels. Furthermore, it provides recommendations regarding the standardization of analysis and reporting, analytical aspects relevant for assessing risks associated with Neu5Gc-containing biotherapeutics, and approaches to minimize Neu5Gc incorporation in recombinant protein manufacturing.
由于非人类 N-羟乙酰神经氨酸(Neu5Gc)的免疫原性及其在人类中高频率存在预先存在的抗-Neu5Gc 抗体,将其纳入治疗性重组蛋白引起了临床关注。关于含有 Neu5Gc 的生物治疗药物的实际影响,科学文献存在分歧,因为目前上市的生物治疗药物并未明确将 Neu5Gc 归因于严重的不良反应临床表现。本文讨论了含有 Neu5Gc 的聚糖在药物清除、预先存在的抗体识别方面的结构和功能考虑因素,以及关于对低 Neu5Gc 水平的耐受性的最新假设。此外,它还就分析和报告的标准化、评估与含有 Neu5Gc 的生物治疗药物相关风险的分析方面,以及最小化重组蛋白生产中 Neu5Gc 掺入的方法提供了建议。