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Immunobiology ; 214(6): 467-74, 2009.
Article in English | MEDLINE | ID: mdl-19150742

ABSTRACT

Recombinant replicons of Semliki Forest virus (SFV) can be used to induce high-level, transient expression of heterologous proteins in vivo. We constructed infectious but replication-deficient SFV particles carrying recombinant RNA encoding the Brucella abortus translation initiation factor 3 (IF3). The recombinant SFV particles (SFV-IF3 particles) were then evaluated for their ability to induce immune responses and to protect BALB/c mice against a challenge with B. abortus 2308 following vaccination. Animals inoculated with SFV-IF3 developed IF3-specific IgM antibodies at day 14 post-immunization. In vitro stimulation of splenocytes from vaccinated mice with either recombinant IF3 (rIF3) or crude Brucella protein extracts resulted in a T-cell proliferative response and induction of interferon gamma secretion, but not interleukin-4. In addition, mice immunized with SFV-IF3 exhibited a significant level of resistance against challenge with the virulent B. abortus strain 2308 (P<0.01). These findings indicate that an SFV-based vector carrying RNA encoding Brucella IF3 has potential for use as a vaccine to induce protection against B. abortus infections.


Subject(s)
Alphavirus Infections/immunology , Eukaryotic Initiation Factors/immunology , Prokaryotic Initiation Factor-3/immunology , Semliki forest virus/immunology , Vaccination , Alphavirus Infections/prevention & control , Animals , Brucella abortus/genetics , Eukaryotic Initiation Factors/genetics , Genetic Engineering , Immunity, Active/genetics , Mice , Mice, Inbred BALB C , Prokaryotic Initiation Factor-3/genetics , Recombination, Genetic , Semliki forest virus/pathogenicity , Virulence
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