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ABSTRACT: Background
CD4+ T-cell epitopes play a crucial role in eliciting vigorous protective immune responses during peptide (epitope)-based vaccination. The prediction of these epitopes focuses on the peptide binding process by MHC class II proteins. The ability to account for MHC class II polymorphism is critical for epitope-based vaccine design tools, as different allelic variants can have different peptide repertoires. In addition, the specificity of CD4+ T-cells is often directed to a very limited set of immunodominant peptides in pathogen proteins. The ability to predict what epitopes are most likely to dominate an immune response remains a challenge.Results
We developed the computational tool Predivac to predict CD4+ T-cell epitopes. Predivac can make predictions for 95% of
SUBMITTER: Oyarzun P
PROVIDER: S-EPMC3598884 | biostudies-literature | 2013 Feb
REPOSITORIES: biostudies-literature