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Development of Production Technology of Live Measles Vaccine for Peroral Administration

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Abstract

According to modern views, an ideal vaccine must provide a life-long immunization effect in 100% of the vaccinated persons, should be safe, thermostable, cheap, and should not be administered parenterally. As known, the most important feature of live vaccines against respiratory infections is rapid development of local secretory immunity in the portal of respiratory and intestinal tracts. We have developed a new technology for production of peroral live measles vaccine where a special attention is paid to optimization of biological stabilizers. The vaccine trials in rabbits, the tablet and capsule forms of the preparation being administered intraduodenally, revealed a stimulation of humoral and cellular immunity and demonstrated the absence of side effects.

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Reference

  1. Krasnova VN (1989) Abstracts of Candidate thesis, Moskow, The Russia.

    Google Scholar 

  2. Bektimirow TA (1990) Actual problems of global measles liquidation.ZhMEI 9, 104–108, The Russia.

    Google Scholar 

  3. Husband AJ (1993) Novel vaccination.Strategies for the control of mucosal infection.Vaccine 11(2), 107–112.

    Article  CAS  PubMed  Google Scholar 

  4. Taros LJu (1967) Experience of isolation of measles virus on the monolayer guinea pigs kidney cell cultures and on the chiken fibroblasts. Voprosi virusologii 4, 399–402, The Russia.

    Google Scholar 

  5. Stepanova LG, Alekseev SB, Zgursky AA (1986) Isolation and characterization of a new strain of diploid cells from human embrionic lung tissue.Tsitologiya 28(12), 1373–1376. The Russia.

    CAS  Google Scholar 

  6. State Pharmacopeia of the USSR (1987), 11 ed., The Russia.

    Google Scholar 

  7. TPC 42-179 VS-94 (1994) “Live dry culture measles vaccine”, The Russia.

    Google Scholar 

  8. Voller A, Bidwell D, Bartlett D (1976) Microplate enzyme immunoassays for the immunodiagnosis of virus infections: In Rose NR, Ed. Friedman H.Manual of Clinical Immunology, Washington, DC, American Society for Microbiolgy, PP 506–512.

    Google Scholar 

  9. Nait S (1988) Analysis of Lymphocyte proliferation.In: Klaus GGB (Ed.) Lymphocytes A practical approach, IRL, Press, Oxford, Washington DC, pp 286–311.

    Google Scholar 

  10. Andries K, Rombaunt B, Dewidt B (1994) Discrepancy bettwen infectivity and antigenicity stabilization of oral poliovirus vaccine a capsid-Unding compound. J. Virol 68(5), 3397–4000.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Grillner L (1976) Immunity of intranasal challenge with rubella virus two years after vaccination comparison of three vaccines J. Infec. Diseases 133(6), 637–642.

    Article  CAS  Google Scholar 

  12. Freestone D, Kelly A, Ferris S, Simmons R (1980) Comparison of antibody responses and virus sheadding following administration on of trivalent oral polyomyolitis vaccines prepared either on monkey kidney or human diploid substrates. J. Hug 84(1), 17–28.

    Article  CAS  Google Scholar 

  13. Sabin A, Arechigo A, Fernandez de Castro (1983) Succeful immunization of infants with and without material antobody by aerosolized measles vaccine.JAMA 249, 2651–2662.

    Article  CAS  PubMed  Google Scholar 

  14. Yuminova NV, Krasnova VP, Ljashenko VA (1993) Specific activity and immunologic sabety of intranasal revaccination with live measles vaccine of Leningrad-16 strain.Voprosii Virusologii 3, 111-113, The Russia.

    Google Scholar 

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© 1997 Springer Science+Business Media Dordrecht

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Nechaeva, E.A. et al. (1997). Development of Production Technology of Live Measles Vaccine for Peroral Administration. In: Carrondo, M.J.T., Griffiths, B., Moreira, J.L.P. (eds) Animal Cell Technology. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5404-8_32

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  • DOI: https://doi.org/10.1007/978-94-011-5404-8_32

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6273-2

  • Online ISBN: 978-94-011-5404-8

  • eBook Packages: Springer Book Archive

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