Systematic development of temperature shift strategies for Chinese hamster ovary cells based on short duration cultures and kinetic modeling

MAbs. 2019 Jan;11(1):191-204. doi: 10.1080/19420862.2018.1525262. Epub 2018 Oct 2.

Abstract

Temperature shift (TS) to a hypothermic condition has been widely used during protein production processes that use Chinese hamster ovary (CHO) cells. The effect of temperature on cell growth, metabolites, protein titer and quality depends on cell line, product, and other bioreactor conditions. Due to the large numbers of experiments, which typically last 2-3 weeks each, limited systematic TS studies have been reported with multiple shift temperatures and steps at different times. Here, we systematically studied the effect of temperature on cell culture performance for the production of two monoclonal antibodies by industrial GS and DG44 CHO cell lines. Three 2-8 day short-duration methods were developed and validated for researching the effect of many different temperatures on CHO cell culture and quality attributes. We found that minor temperature differences (1-1.5 °C) affected cell culture performance. The kinetic parameters extracted from the short duration data were subsequently used to compute and predict cell culture performance in extended duration of 10-14 days with multiple TS conditions for both CHO cell lines. These short-duration culture methods with kinetic modeling tools may be used for effective TS optimization to achieve the best profiles for cell growth, metabolites, titer and quality attributes. Although only three short-duration methods were developed with two CHO cell lines, similar short-duration methods with kinetic modeling may be applied for different hosts, including both microbial and other mammalian cells.

Keywords: CHO cell culture; kinetic modeling; process development; quality attributes; short duration method; specific productivity; temperature shift; titer.

MeSH terms

  • Animals
  • Antibodies, Monoclonal*
  • Bioreactors / standards
  • CHO Cells*
  • Cell Culture Techniques / methods*
  • Cell Proliferation
  • Cricetinae
  • Cricetulus
  • Kinetics
  • Temperature

Substances

  • Antibodies, Monoclonal