Induction of tumor-specific CTL responses using the C-terminal fragment of Viral protein R as cell penetrating peptide.

ABSTRACT: The discovery of tumor-associated antigens recognized by T lymphocytes opens the possibility of vaccinating cancer patients with defined antigens. However, one of the major limitation of peptide-based vaccines is the low immunogenicity of antigenic peptides. Interestingly, if these epitopes are directly delivered into the cytoplasm of antigen presenting cells, they can be efficiently presented via the direct MHC class I presentation pathway. To improve antigen entry, one promising approach is the use of cell penetrating peptides (CPPs). However, most studies use a covalent binding of the CPP with the antigen. In the present study, we focused on the C-terminal domain of Vpr which was previously demonstrated to efficiently deliver plasmid DNA into cells. We provide evidence that the peptides

SUBMITTER: Gross DA 

PROVIDER: S-EPMC6408526 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature