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Comparative Assessment of the Structural Features of Originator Recombinant Human Follitropin Alfa Versus Recombinant Human Follitropin Alfa Biosimilar Preparations Approved in Non-European Regions

Authors :
Lucio Manzi
Nunzio Sepe
Walter Migliaccio
Ludovica Lanzoni
Luisa Iozzino
Fabrizia D’Angelo
Lucia Colarusso
Susana Montenegro
Angelo Palmese
Thomas D’Hooghe
Alfredo Ulloa-Aguirre
Yulia Koloda
Monica Lispi
Source :
International Journal of Molecular Sciences; Volume 23; Issue 12; Pages: 6762
Publication Year :
2022
Publisher :
MDPI, 2022.

Abstract

Although the full primary structures of the alfa and beta subunits of reference r-hFSH-alfa and its biosimilars are identical, cell context-dependent differences in the expressing cell lines and manufacturing process can lead to variations in glycosylation profiles. In the present study, we compared the structural features of reference r-hFSH-alfa with those of five biosimilar preparations approved in different global regions outside Europe (Primapur®, Jin Sai Heng®, Follitrope®, Folisurge®, and Corneumon®) with respect to glycosylation, macro- and microheterogeneity, and other post-translational modifications and higher order structure. The mean proportion of N-glycosylation-site occupancy was highest in reference r-hFSH-alfa, decreasing sequentially in Primapur, Jin Sai Heng, Corneumon, Follisurge and Follitrope, respectively. The level of antennarity showed slightly higher complexity in Corneumon, Primapur and Follitrope versus reference r-hFSH-alfa, whereas Jin Sai Heng and Folisurge were aligned with reference r-hFSH-alfa across all N-glycosylation sites. Sialylation level was higher in Corneumon and Follitrope, but small differences were detected in other biosimilar preparations compared with reference r-hFSH-alfa. Jin Sai Heng showed higher levels of N-glyconeuramic acid than the other preparations. Minor differences in oxidation levels were seen among the different products. Therefore, in summary, we identified var ious differences in N-glycosylation occupancy, antennarity, sialylation and oxidation between reference r-hFSH-alfa and the biosimilar preparations analyzed. ispartof: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES vol:23 issue:12 ispartof: location:Switzerland status: published

Details

Language :
English
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences; Volume 23; Issue 12; Pages: 6762
Accession number :
edsair.doi.dedup.....266008041c927d7629af795674928ca5