Industrial production of monoclonal antibodies and therapeutic proteins by dialysis fermentation (original) (raw)

Abstract

A novel and powerful fermentation method is reported for the large-scale growth of mammalian cells and their secreted products. The system described illustrates many of the advantages of conventional batch fermentation processes but in addition has been shown to yield cell densities in excess of 1×107 cells/ml with concomitant increase in product concentration.

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Abbreviations

MAb:

Monoclonal Antibody

STR:

Stirred Tank Reactor

FBS:

Foetal Bovine Serum

References

  1. Berg GJ and Bödeker BGD (1988) Employing a ceramic matrix for the immobilization of mammalian cells in culture. In: Spier RE and Griffiths JB (eds.) Animal Cell Biotechnology, Vol. 3, pp. 321–335. Academic Press, London.
    Google Scholar
  2. Birch JR and Cartwright T (1982) Environmental factors influencing the growth of animal cells in culture. J. Chem. Tech. Biotechnol. 32: 313–317.
    Google Scholar
  3. Kearns MJ, Comer MJ, Steegmans U and Jungfer H (1985) Boehringer Mannheim GmbH, German patent: DE 3541738.
  4. Kearns MJ, Comer MJ, Steegmans U and Jungfer H (1986) Boehringer Mannheim GmbH, European patent: EP 0224800A2.
  5. Knazek RA, Gullino PM, Kohler PO and Dedrick RL (1972) Cell culture on artificial capillaries: an approach to tissue growth in vitro. Science 178: 65–66.
    Google Scholar
  6. Köhler G and Milstein C (1975) Continuous culture of fused cells secreting antibody of predefined specificity. Nature 256: 495–597.
    Google Scholar
  7. Lim F and Sun AM (1980) Microencapsulated islets as bioartificial endocrine pancreas. Science 210: 908–910.
    Google Scholar
  8. Reuveny S, Velez D, Macmillan JD and Miller L (1986) Factors affecting cell growth and monoclonal antibody production in stirred reactors. J. Immuno. Methods 86: 53–59.
    Google Scholar
  9. Schonberg J and Belfort G (1987) Enhanced nutrient transport in hollow-fibre perfusion bioreactors a theoretical analysis. Biotechnol. Progress 3: 80–89.
    Google Scholar
  10. Tolbert WR, Feder J and Kimes RC (1981) Large-scale rotating filter perfusion system for high density growth of mammalian suspension cells. In Vitro 17: 885–890.
    Google Scholar
  11. Van Wezel AL (1967) Growth of cell strains and primary cells on microcarriers in homogeneous culture. Nature 216: 64–65.
    Google Scholar

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Authors and Affiliations

  1. Research Centre Penzberg, Boehringer Mannheim GmbH, Nonnenwald, 8122, Penzberg, Germany
    Michael J. Comer, Michael J. Kearns, Jürgen Wahl, Michael Munster, Thomas Lorenz, Berthold Szperalski, Stefan Koch, Ulrich Behrendt & Herwig Brunner

Authors

  1. Michael J. Comer
  2. Michael J. Kearns
  3. Jürgen Wahl
  4. Michael Munster
  5. Thomas Lorenz
  6. Berthold Szperalski
  7. Stefan Koch
  8. Ulrich Behrendt
  9. Herwig Brunner

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Comer, M.J., Kearns, M.J., Wahl, J. et al. Industrial production of monoclonal antibodies and therapeutic proteins by dialysis fermentation.Cytotechnology 3, 295–299 (1990). https://doi.org/10.1007/BF00365493

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