Kwon Joon-Cheol, Kwon O Hwan, Jeong Rae Ung, Kim Nayoun, Song Seonah, Choi Ilsub, Lee Juneok, Horiuchi Takahiko
Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Life Science R&D campus, LG Science Park, LG Chem, Ltd., Seoul, Republic of Korea.
Anim Cells Syst (Seoul). 2021 Jun 23;25(3):182-194. doi: 10.1080/19768354.2021.1943709. eCollection 2021.
LBAL was developed as an adalimumab (Humira®) biosimilar using Chinese hamster ovary cell lines. Comparable quality, safety, and efficacy between a biosimilar and its reference product should be ensured for regulatory approval. Here, we present the results of a comprehensive physicochemical and biological characterization between LBAL and Humira®. As physicochemical attributes, primary and higher-order structure, -glycan profile, and disulfide linkage were investigated. Biological attributes were evaluated by target/receptor binding analysis and / cell-based assays, which are linked to mechanisms of action. As a result, LBAL had the identical amino acid sequence, similar post-translational modifications and N-/C-terminal variants, and comparable primary, secondary, and tertiary structures and disulfide linkage profile. However, some differences in -glycan profiles were observed. Biological activities, including tumor necrosis factor (TNF) binding, TNF-neutralization, apoptosis, Fc receptor binding, and complement-dependent cytotoxicity, were largely consistent. Despite a slightly lower antibody-dependent cellular cytotoxicity activity in LBAL, this difference was not significant under physiological conditions. As indicated, this extensive analytical characterization and functional comparison assessment showed that LBAL was similar to Humira®, with minor differences of no clinical relevance. Taken together, our comparative assessment of physicochemical and biological attributes demonstrated that LBAL is structurally and functionally very similar to Humira®, supporting the biosimilarity of clinical efficacy and safety.
LBAL是一种使用中国仓鼠卵巢细胞系开发的阿达木单抗(修美乐®)生物类似药。为获得监管批准,应确保生物类似药与其参照产品在质量、安全性和有效性方面具有可比性。在此,我们展示了LBAL与修美乐®之间全面的物理化学和生物学特性分析结果。作为物理化学属性,研究了一级和高级结构、聚糖谱和二硫键。通过与作用机制相关的靶点/受体结合分析和基于细胞的试验对生物学属性进行了评估。结果显示,LBAL具有相同的氨基酸序列、相似的翻译后修饰和N-/C-末端变体,以及可比的一级、二级和三级结构和二硫键谱。然而,观察到聚糖谱存在一些差异。包括肿瘤坏死因子(TNF)结合、TNF中和、细胞凋亡、Fc受体结合和补体依赖性细胞毒性在内的生物学活性基本一致。尽管LBAL中的抗体依赖性细胞毒性活性略低,但在生理条件下这种差异并不显著。如前所述,这种广泛的分析特性和功能比较评估表明,LBAL与修美乐®相似,存在一些无临床相关性的细微差异。综上所述,我们对物理化学和生物学属性的比较评估表明,LBAL在结构和功能上与修美乐®非常相似,支持其临床疗效和安全性的生物相似性。