Applied Microbiology and Biotechnology

, Volume 96, Issue 4, pp 885–894

Recent advances in technology supporting biopharmaceutical production from mammalian cells


DOI: 10.1007/s00253-012-4451-z

Cite this article as:
Butler, M. & Meneses-Acosta, A. Appl Microbiol Biotechnol (2012) 96: 885. doi:10.1007/s00253-012-4451-z


The demand for production of glycoproteins from mammalian cell culture continues with an increased number of approvals as biopharmaceuticals for the treatment of unmet medical needs. This is particularly the case for humanized monoclonal antibodies which are the largest and fastest growing class of therapeutic pharmaceuticals. This demand has fostered efforts to improve the efficiency of production as well as to address the quality of the final product. Chinese hamster ovary cells are the predominant hosts for stable transfection and high efficiency production on a large scale. Specific productivity of recombinant glycoproteins from these cells can be expected to be above 50 pg/cell/day giving rise to culture systems with titers of around 5 g/L if appropriate fed-batch systems are employed. Cell engineering can delay the onset of programmed cell death to ensure prolonged maintenance of productive viable cells. The clinical efficacy and quality of the final product can be improved by strategic metabolic engineering. The best example of this is the targeted production of afucosylated antibodies with enhanced antibody-dependent cell cytotoxicity, an important function for use in cancer therapies. The development of culture media from non-animal sources continues and is important to ensure products of consistent quality and without the potential danger of contamination. Process efficiencies may also be improved by employing disposable bioreactors with the associated minimization of downtime. Finally, advances in downstream processing are needed to handle the increased supply of product from the bioreactor but maintaining the high purity demanded of these biopharmaceuticals.


Biopharmaceuticals CHO cells Glycosylation Apoptosis Antibodies Vaccines 

Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  1. 1.Department of MicrobiologyUniversity of ManitobaWinnipegCanada
  2. 2.Pharmaceutical Biotechnology Lab., Faculty of PharmacyUniversidad Autónoma del Estado de MorelosMorelosMexico