Comparative pharmacology of a new recombinant FSH expressed by a human cell line

Wolfgang Koechling*, Daniel Plaksin, Glenn E. Croston, Janni V. Jeppesen, Kirsten T. Macklon, Claus Yding Andersen

*Corresponding author for this work

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Abstract

Recombinant FSH proteins are important therapeutic agents for the treatment of infertility, including follitropin alfa expressed in Chinese Hamster Ovary (CHO) cells and, more recently, follitropin delta expressed in the human cell line PER.C6. These recombinant FSH proteins have distinct glycosylation, and have distinct pharmacokinetic and pharmacodynamic profiles in women. Comparative experiments demonstrated that follitropin delta and follitropin alfa displayed the same in vitro potency at the human FSH receptor, but varied in their pharmacokinetics in mouse and rat. While follitropin delta clearance from serum depended in part on the hepatic asialoglycoprotein receptor (ASGPR), follitropin alfa clearance was unaffected by ASGPR inhibition in rat or genetic ablation in mice. The distinct properties of follitropin delta and follitropin alfa are likely to contribute to the differing pharmacokinetic and pharmacodynamic profiles observed in women and to influence their efficacy in therapeutic protocols for the treatment of infertility.

Original languageEnglish
JournalEndocrine Connections
Volume6
Issue number5
Pages (from-to)297-305
ISSN2049-3614
DOIs
Publication statusPublished - 2017

Keywords

  • Follicle-stimulating hormone
  • Follitropin delta
  • FSH glycosylation
  • Gonadotropin clearance
  • Recombinant FSH

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