Position-Scanning Peptide Libraries as Particle Immunogens for Improving CD8⁺ T-Cell Responses.

ABSTRACT: Short peptides reflecting major histocompatibility complex (MHC) class I (MHC-I) epitopes frequently lack sufficient immunogenicity to induce robust antigen (Ag)-specific CD8⁺ T cell responses. In the current work, it is demonstrated that position-scanning peptide libraries themselves can serve as improved immunogens, inducing Ag-specific CD8⁺ T cells with greater frequency and function than the wild-type epitope. The approach involves displaying the entire position-scanning library onto immunogenic nanoliposomes. Each library contains the MHC-I epitope with a single randomized position. When a recently identified MHC-I epitope in the glycoprotein gp70 envelope protein of murine leukemia virus (MuLV) is assessed, only one of the eight positional libraries tested, rand

SUBMITTER: He X 

PROVIDER: S-EPMC8693074 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature