Design of cross-reactive antigens with machine learning and high-throughput experimental evaluation.
Ontology highlight
ABSTRACT: Selecting an optimal antigen is a crucial step in vaccine development, significantly influencing both the vaccine's effectiveness and the breadth of protection it provides. High antigen sequence variability, as seen in pathogens like rhinovirus, HIV, influenza virus, complicates the design of a single cross-protective antigen. Consequently, vaccination with a single antigen molecule often confers protection against only a single variant. In this study, machine learning methods were applied to the design of factor H binding protein (fHbp), an antigen from the bacterial pathogen Neisseria meningitidis. The vast number of potential antigen mutants presents a significant challenge for improving fHbp antigenicity. Moreover, limited data on antigen-antibody binding in public databases con
SUBMITTER: Chesterman C
PROVIDER: S-EPMC12319226 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature
ACCESS DATA