Recent advances in the production of recombinant factor IX: bioprocessing and cell engineering.

Chinese hamster ovary cell bioprocessing cell engineering factor IX production post-translational modifications recombinant factor IX

Journal

Critical reviews in biotechnology
ISSN: 1549-7801
Titre abrégé: Crit Rev Biotechnol
Pays: England
ID NLM: 8505177

Informations de publication

Date de publication:
May 2023
Historique:
medline: 7 4 2023
pubmed: 19 4 2022
entrez: 18 4 2022
Statut: ppublish

Résumé

Appropriate treatment of Hemophilia B is vital for patients' quality of life. Historically, the treatment used was the administration of coagulation Factor IX derived from human plasma. Advancements in recombinant technologies allowed Factor IX to be produced recombinantly. Successful recombinant production has triggered a gradual shift from the plasma derived origins of Factor IX, as it provides extended half-life and expanded production capacity. However, the complex post-translational modifications of Factor IX have made recombinant production at scale difficult. Considerable research has therefore been invested into understanding and optimizing the recombinant production of Factor IX. Here, we review the evolution of recombinant Factor IX production, focusing on recent developments in bioprocessing and cell engineering to control its post-translational modifications in its expression from Chinese Hamster Ovary (CHO) cells.

Identifiants

pubmed: 35430942
doi: 10.1080/07388551.2022.2036691
doi:

Substances chimiques

Factor IX 9001-28-9
Recombinant Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

484-502

Auteurs

Aiden C Beauglehole (AC)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.
CSL Innovation, Parkville, Victoria, Australia.

Dinora Roche Recinos (D)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.
CSL Innovation, Parkville, Victoria, Australia.

Cassandra L Pegg (CL)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.

Yih Yean Lee (YY)

CSL Innovation, Parkville, Victoria, Australia.

Victor Turnbull (V)

CSL Innovation, Bio21 Institute of Molecular Science and Biotechnology, Parkville, Victoria, Australia.

Susann Herrmann (S)

CSL Innovation, Bio21 Institute of Molecular Science and Biotechnology, Parkville, Victoria, Australia.

Esteban Marcellin (E)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.

Christopher B Howard (CB)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.

Benjamin L Schulz (BL)

ARC Training Centre for Biopharmaceutical Innovation, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St. Lucia, QLD, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, Queensland, Australia.

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Classifications MeSH