From: Combination strategies to maximize the benefits of cancer immunotherapy
Technology | Examples | Important considerations |
---|---|---|
Peptides | Short peptide (< 15 aa) | Directly binding to MHC, Not processed by APC, more tolerogenic, |
Synthetic long peptide, neoantigens | Preferably taken up and processed by dendritic cells, usually co-administrated with adjuvant to potentiate immunogenicity | |
Cellular vaccine | Tumor cells | Autologous or allogeneic, not need to identify tumor antigens, |
Dendritic cells | Provide tumor antigens and costimulatory signals, can co-express cytokines and other co-stimulatory molecules, highly immunogenic | |
Microorganisms | Microorganisms are immunostimulatory, can co-express other stimulatory molecules | |
Viral vector | PROSTVAC-VF/Tricom | Vehicles are highly immunogenic, can co-express stimulatory cytokines and other molecules; may need local injection; neutralizing antibody can clear virus |
DNA/RNA | RNA mutanome vaccines | Vaccine (DNA/RNA) itself is immunogenic. Low delivery efficiency with the native form. Other delivery methods (nanoparticles, gene gun and in situ electroporation) enhance delivery |