Personalized Neoantigen Vaccines: Dendritic Cells, mRNA, and Peptides Advance Cancer Immunotherapy via Rational Combinations
Background
Cancer immunotherapy faces significant hurdles, with limited efficacy hindering the widespread clinical translation of therapeutic vaccines. Despite advancements, Sipuleucel-T remains the sole FDA-approved therapeutic cancer vaccine, underscoring a critical gap. Current neoantigen prediction strategies for peptide vaccines often yield low immune response rates, with only 10-20% of selected peptides inducing responses in patients. This highlights a pressing need for more effective antigen selection and delivery methods. Personalized vaccines, by targeting patient-specific neoantigens, offer a promising strategy to overcome these limitations and optimize immune responses, particularly by leveraging platforms like peptide, mRNA, and dendritic cell (DC) vaccines to induce potent antitumor T-cell responses.