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Virology ; 519: 33-41, 2018 06.
Article in English | MEDLINE | ID: mdl-29631174

ABSTRACT

Hepatitis C virus (HCV) is a globally disseminated human pathogen for which no vaccine is currently available. HCV is highly diverse genetically and can be classified into 7 genotypes and multiple sub-types. Due to this antigenic variation, the induction of cross-reactive and at the same time neutralizing antibodies is a challenge in vaccine production. Here we report the analysis of immunogenicity of recombinant HCV envelope glycoproteins from genotypes 1a, 1b and 2a, with a Flag tag inserted in the hypervariable region 1 of E2. This modification did not affect protein expression or conformation or its capacity to bind the crucial virus entry factor, CD81. Importantly, in immunogenicity studies on mice, the purified E2-Flag mutants elicited high-titer, cross-reactive antibodies that were able to neutralize HCV infectious particles from two genotypes tested (1a and 2a). These findings indicate that E1E2-Flag envelope glycoproteins could be important immunogen candidates for vaccine aiming to induce broad HCV-neutralizing responses.


Subject(s)
Antibodies, Neutralizing/immunology , Antibodies, Viral/immunology , Hepacivirus/immunology , Viral Envelope Proteins/immunology , Animals , Antibodies, Neutralizing/biosynthesis , Cell Line , Cross Reactions , Epitope Mapping , Epitopes/immunology , Genotype , Hepacivirus/genetics , Hepacivirus/physiology , Humans , Immunogenicity, Vaccine , Mice , Neutralization Tests , Receptors, Virus/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/immunology , Tetraspanin 28/metabolism , Viral Envelope Proteins/chemistry , Viral Envelope Proteins/genetics , Viral Envelope Proteins/metabolism , Virus Internalization
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