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An inactivated poliovirus vaccine using Sabin strains produced on the serum-free PER.C6® cell culture platform is immunogenic and safe in a non-human primate model.
Bockstal, Viki; Tiemessen, Machteld M; Achterberg, Rogier; Van Wordragen, Carlo; Knaapen, Ad M; Serroyen, Jan; Marissen, Wilfred E; Schuitemaker, Hanneke; Zahn, Roland.
Afiliación
  • Bockstal V; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Tiemessen MM; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Achterberg R; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Van Wordragen C; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Knaapen AM; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Serroyen J; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Marissen WE; Merus N.V., Yalelaan 62, 3584 CM Utrecht, the Netherlands(2).
  • Schuitemaker H; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands.
  • Zahn R; Janssen Vaccines and Prevention BV, Archimedesweg 4-6, 2333CN Leiden, the Netherlands. Electronic address: rzahn@its.jnj.com.
Vaccine ; 36(46): 6979-6987, 2018 11 12.
Article en En | MEDLINE | ID: mdl-30314910
BACKGROUND: The World Health Organization recommends the development of affordable next-generation inactivated poliovirus vaccines (IPV) using attenuated poliovirus Sabin strains. Previously, we introduced a novel PER.C6® cell culture platform, which allows for high yield production of an affordable trivalent Sabin IPV vaccine. METHODS: Immunogenicity and safety of this novel PER.C6®-based Sabin-IPV (sIPV) was assessed in rats and non-human primates (NHPs). NHPs received one of four different dose dilutions vaccine according to current human schedule (three prime-immunizations and one boost immunization). For comparison, NHPs received commercially available reference Salk IPV or sIPV. RESULTS: Dose-dependent immunogenicity and good tolerability was observed for the PER.C6®-based sIPV formulations in rats and NHPs. In NHPs, the lowest tested dose that induced anti-Sabin virus-neutralizing antibody titers that were non-inferior to commercial sIPV after three immunizations was 5-7.5-25 D-antigen units for type 1, 2 and 3 respectively. DISCUSSION: PER.C6®-based sIPV induced comparable immunogenicity to commercial Salk IPV and sIPV vaccines in NHPs. Together with the absence of any preclinical safety signals, these data warrant further testing in clinical trials. sIPV produced on the PER.C6® cell platform could be one solution to the need for an affordable and immunogenic IPV to achieve and maintain global polio eradication.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Vacuna Antipolio de Virus Inactivados / Poliovirus Límite: Animals Idioma: En Revista: Vaccine Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Vacuna Antipolio de Virus Inactivados / Poliovirus Límite: Animals Idioma: En Revista: Vaccine Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos