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多方面评估利妥昔单抗生物类似药:糖基化微不均一性对 Fc 功能的影响。

Multifaceted assessment of rituximab biosimilarity: The impact of glycan microheterogeneity on Fc function.

机构信息

Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109, United States; Biointerfaces Institute, University of Michigan, Ann Arbor, MI 48109, United States.

Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.

出版信息

Eur J Pharm Biopharm. 2020 Jan;146:111-124. doi: 10.1016/j.ejpb.2019.12.003. Epub 2019 Dec 10.

Abstract

Biosimilars are poised to reduce prices and increase patient access to expensive, but highly effective biologic products. However, questions still remain about the degree of similarity and scarcity of information on biosimilar products from outside of the US/EU in the public domain. Thus, as an independent entity, we performed a comparative analysis between the innovator, Rituxan® (manufactured by Genentech/Roche), and a Russian rituximab biosimilar, Acellbia® (manufactured by Biocad). We evaluated biosimilarity of these two products by a variety of state-of-the-art analytical mass spectrometry techniques, including tandem MS mapping, HX-MS, IM-MS, and intact MS. Both were found to be generally similar regarding primary and higher order structure, though differences were identified in terms of glycoform distribution levels of C-terminal Lys, N-terminal pyroGlu, charge variants and soluble aggregates. Notably, we confirmed that the biosimilar had a higher level of afucosylated glycans, resulting in a stronger FcγIIIa binding affinity and increased ADCC activity. Taken together, our work provides a comprehensive comparison of Rituxan® and Acellbia®.

摘要

生物类似药有望降低价格,并增加患者获得昂贵但高效的生物制品的机会。然而,关于美国/欧盟以外的生物类似药产品的相似程度和信息稀缺性问题仍然存在。因此,作为一个独立实体,我们对创新药物利妥昔单抗(由罗氏/基因泰克生产)和俄罗斯的利妥昔单抗生物类似药阿塞利布(由 Biocad 生产)进行了比较分析。我们使用各种最先进的分析质谱技术,包括串联 MS 图谱、HX-MS、IM-MS 和完整 MS,评估了这两种产品的生物类似性。结果发现,这两种产品在一级和高级结构方面总体相似,但在 C 末端赖氨酸、N 末端焦谷氨酸、电荷变体和可溶性聚集体的糖型分布水平方面存在差异。值得注意的是,我们证实生物类似药具有更高水平的去岩藻糖基化聚糖,导致更强的 FcγIIIa 结合亲和力和增加的 ADCC 活性。总之,我们的工作提供了对利妥昔单抗和阿塞利布的全面比较。

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