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Choice of Cell Substrate for Biological Products

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Cell Substrates

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 118))

Abstract

The methods at present adopted for the control of the substrate for production of modified live virus vaccines are well established. They involve maintaining colonies of chickens, ducks or rabbits which are the source of primary cells for making such vaccines. These colonies are regularly monitored to exclude infections. The use of human diploid cell lines like WI38 and MRC5 are now internationally accepted as satisfactory substrates for these vaccines and bring the benefits of a defined seed system to the cell substrates as well as to the virus seed. These benefits are consistency and stability; and the ability to use a pretested seed.

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References

  1. Capstick P.B., Garland A.J., Chapman W.G., et al. Production of foot and mouth disease virus antigen from BHK 21 clone 13 cells grown and infected in Deep Suspension Cultures. Nature 205:1135–1136, 1965.

    Article  PubMed  CAS  Google Scholar 

  2. Keeble S.A. and Heymann C.S.. Effect of ß-Propiolactone and Thiomersal on Growth of B.H.K. cells in the Hamster Cheek Pouch. Nature 208:1125–1126, 1965.

    Article  PubMed  CAS  Google Scholar 

  3. Report. Committee on Tissue Culture Viruses and Vaccines. Continuously cultured tissue cells and Viral Vaccines. Science 139:15–20, 1963.

    Article  Google Scholar 

  4. Pirquet C.F., and Schick B. Serum Sickness. Translated by Bela Schick. Wiliams Wilkins, Baltimore, 1951.

    Google Scholar 

  5. Hull R.N., Minner J.R. and Mascoli G.C New agents recovered from tissue cultures of monkey kidney cells. III. Recovery of additional agents both from cultures of monkey kidney tissues and directly from tissues and excreta. American Journal of Hygiene 68: 31–44, 1959.

    Google Scholar 

  6. Stones P.B. Production and control of live oral poliovirus vaccine in WI-38 human diploid cells. Joint WHO/IABS Symposium on the standardization of cell substrates for the production of virus vaccines, Geneva, Dec. 1976. Develop. biol. Standard., 37: 251–253. S. Karger, Basel 1977.

    Google Scholar 

  7. Christofinis G.J. and Finter N.B. The preparation of Interferon from lymphoblastoid cell lines. Proceedings of Symposium. Preparation, Standardization and clinical use of Interferon. Zagreb, June 8–9, 1977.

    Google Scholar 

  8. Pritchett R., Pedersen M. and Kieff E. Complexity of EBV homologous DNA in continuous lymphoblastoid cell lines. Virology 74:227–231. 1976.

    Article  Google Scholar 

  9. Nilsson K., Giovanella B.C., Stehlin F.S. and Klein J. Tumorgenicity of human hematropoietic cell lines in Athymic mice. Inst. of Cancer, 19:337–344, 1977.

    Article  CAS  Google Scholar 

  10. Fantes K.H. Workshop on Clinical Trials with Interferon. National Institute of Allergy and Infectious Diseases and National Cancer Institute, Bethesda. March 21–23, 1978.

    Google Scholar 

  11. Hughes M., Thomson, R.O., Knight P., and Stephen J. The Immunopurification of Tetanus Toxoid. J. Applied Bacteriology 37:603–621, 1974.

    Article  CAS  Google Scholar 

  12. Beale, A.J. D antigen content in poliovaccine as a measure of potency. Lancet 2:1166, 1961.

    Google Scholar 

  13. Salk J., Cohen H., Fillastre, et al. Killed poliovirus antigen titration in humans. Developments in Biological Standardization: Standardization and use of vaccines in the developing countries. Proceedings 15th International congress, April 1978. International Association of Biological Standardization (in press).

    Google Scholar 

  14. van Wezel A.L., van Steenis G., Hannick Ch.A. and Cohen H. Developments in Biological Standardization: Standardization and use of vaccines in the developing countries. Proceedings 15th International Congress, April 1978. International Association of Biological Standardization (in press).

    Google Scholar 

  15. Pereira H.G., Valentine R.C., and Russell W.C. Crystallization of an Adenovirus Protein (The Hexon). Nature, 219:946–947, 1968.

    Article  PubMed  CAS  Google Scholar 

  16. Mautner V. and Pereira H.G. Crystallization of a second adenovirus Protein (the Fibre). Nature, 230:456–457, 1971.

    Article  PubMed  CAS  Google Scholar 

  17. Haase A.T., Mautner V. and Pereira H.G. The immugenicity of adenovirus type 5 Structural proteins. Journal Immunology, 108: 483–485, 1972.

    CAS  Google Scholar 

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© 1979 Plenum Press, New York

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Beale, A.J. (1979). Choice of Cell Substrate for Biological Products. In: Petricciani, J.C., Hopps, H.E., Chapple, P.J. (eds) Cell Substrates. Advances in Experimental Medicine and Biology, vol 118. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-0997-0_9

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  • DOI: https://doi.org/10.1007/978-1-4684-0997-0_9

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-0999-4

  • Online ISBN: 978-1-4684-0997-0

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