[Safety and immunogenecity of a vaccine of polyssacharide Vi from Salmonella typhi in Cuban youths]

Rev Cubana Med Trop. 2003 May-Aug;55(2):83-7.
[Article in Spanish]

Abstract

A randomized, controlled and double-blind study was conducted in young adults aged 18-20 aimed at evaluating the reactogenecity and immunogenecity of vaz-TyVi, a vaccine of polyssacharide Vi from Salmonella typhi. They were distributed into 3 groups: immunized with a dose of Vax-TyVi (Finlay Institute), TYPHIM Vi (Pasteur-Mérieux) or vax-TET (tetanic toxoid). Serum samples were taken before and 21 days after immunization. The immunogenecity was evaluated in 323 volunteers by an indirect ELISA. The seroconversion of those receiving vax-TyVi was 81.97% and 65.05 % for TYPHIM Vi. The postvaccine mean geometric titers were 7.41 U/mL (5.92-9.27 U/mL) and 5.41 U/mL (4.35-6.72 U/mL), respectively. The seroconversion with vax-TET was 0%. The reactogenecity of both polysaccharide vaccines was low. It was concluded that the immunogenecity of vax-TyVi was not lower than that of TYPHIM Vi and that its reactogenecity was similar.

Publication types

  • Clinical Trial
  • English Abstract
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Cuba
  • Double-Blind Method
  • Humans
  • Polysaccharides, Bacterial / immunology*
  • Salmonella Vaccines / immunology*

Substances

  • Polysaccharides, Bacterial
  • Salmonella Vaccines
  • capsular polysaccharide, Salmonella