a Department of Pharmaceutical Sciences , University of Michigan , 428 Church Street, Ann Arbor , MI.
b Biointerfaces Institute, University of Michigan , 2800 Plymouth Road, Ann Arbor , MI.
MAbs. 2017 Oct;9(7):1197-1209. doi: 10.1080/19420862.2017.1347741. Epub 2017 Aug 8.
Remsima™ (infliximab) is the first biosimilar monoclonal antibody (mAb) approved by the European Medical Agency and the US Food and Drug Administration. Remsima™ is highly similar to its reference product, Remicade®, with identical formulation components. The 2 products, however, are not identical; Remsima™ has higher levels of soluble aggregates, C-terminal lysine truncation, and fucosylated glycans. To understand if these attribute differences could be amplified during forced degradation, solutions and lyophilized powders of the 2 products were subjected to stress at elevated temperature (40-60°C) and humidity (dry-97% relative humidity). Stress-induced aggregation and degradation profiles were similar for the 2 products and resulted in loss of infliximab binding to tumor necrosis factor and FcγRIIIa. Appearances of protein aggregates and hydrolysis products were time- and humidity-dependent, with similar degradation rates observed for the reference and biosimilar products. Protein powder incubations at 40°C/97% relative humidity resulted in partial mAb unfolding and increased asparagine deamidation. Minor differences in heat capacity, fluorescence, levels of subvisible particulates, deamidation and protein fragments were observed in the 2 stressed products, but these differences were not statistically significant. The protein solution instability at 60°C, although quite significant, was also similar for both products. Despite the small initial analytical differences, Remicade® and Remsima™ displayed similar degradation mechanisms and kinetics. Thus, our results show that the 2 products are highly similar and infliximab's primary sequence largely defines their protein instabilities compared with the limited influence of small initial purity and glycosylation differences in the 2 products.
Remsima™(英夫利昔单抗)是首个获得欧洲药品管理局和美国食品药品监督管理局批准的生物类似药。Remsima™与参照产品 Remicade®高度相似,具有相同的配方成分。然而,这两种产品并不完全相同;Remsima™具有更高水平的可溶性聚集体、C 末端赖氨酸截断和糖基化的岩藻糖。为了了解这些属性差异在强制降解过程中是否会被放大,对两种产品的溶液和冻干粉末在高温(40-60°C)和高湿度(干燥-97%相对湿度)下进行了应激处理。两种产品的应激诱导聚集和降解谱相似,导致英夫利昔单抗与肿瘤坏死因子和 FcγRIIIa 的结合丢失。蛋白质聚集体和水解产物的出现与时间和湿度有关,参照产品和生物类似产品的降解速率相似。在 40°C/97%相对湿度下孵育蛋白质粉末会导致 mAb 部分展开,并增加天冬酰胺脱酰胺。在两种应激产品中观察到较小的差热容量、荧光、亚可见颗粒水平、脱酰胺和蛋白质片段的差异,但这些差异没有统计学意义。尽管 60°C 下的蛋白质溶液不稳定性非常显著,但两种产品的不稳定性也相似。尽管最初的分析存在微小差异,但 Remicade®和 Remsima™显示出相似的降解机制和动力学。因此,我们的结果表明,这两种产品高度相似,英夫利昔单抗的一级序列在很大程度上决定了它们的蛋白质不稳定性,而产品中最初的微小纯度和糖基化差异的影响有限。