Whole tumor cells |
Complete Ag pool of an individual tumor (including Ags that have not been identified yet) |
Must be made individually for each patient |
Activation of a polyclonal and more effective immune response |
Lack of co-stimulatory molecules on solid tumor cells |
The immune system rather than the vaccinologist selects the most immunogenic tumor-specific Ags |
Immune response difficult to monitor |
Induction of auto-immunity in the presence of adjuvant |
Dendritic cells (DCs) |
Presentation of the vaccine Ags to other cell types of the immune system |
Must be made individually for each patient |
Expression of high levels of HLA complexes and co-stimulatory molecules |
Generation of DCs technically challenging |
Stimulation of both naive and memory T cells |
Money- and time-consuming treatment |
DNA |
Easy and cheap to produce and purify |
DNA integration into the cell genome potentially promoting malignancy |
Require no special handling or storage conditions |
Less effective than peptide vaccines in inducing CD8+ T cell response |
Elicitation of both CD8+ and CD4+ immune responses as well as humoral responses |
Peptides |
Easy to manufacture |
Immune response limited to one or few epitopes |
Strong CD8+ T cell response |
HLA restriction |
Known sequence and biochemistry |
Degradation in the absence of adjuvant |
Allow specific monitoring of the patient’s immune response |
Anti-idiotypic antibodies |
Unrestricted HLA population |
Human anti-mouse antibody response |
Allow effective vaccination against non-protein Ags and poorly immunogenic Ags |
Elicit both humoral and cellular immune response |