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  • Subunit vaccination with no risk for infection[1]
  • Antigen presentation by both MHC class I and class II molecules[1]
  • Able to polarise T-cell help toward type 1 or type 2[1]
  • Immune response focused only on antigen of interest
  • Ease of development and production[1]
  • Stability of vaccine for storage and shipping
  • Cost-effectiveness
  • Obviates need for peptide synthesis, expression and purification of recombinant proteins and the use of toxic adjuvants[8]
  • Long-term persistence of immunogen[2]
  • In vivo expression ensures protein more closely resembles normal eukaryotic structure, with accompanying post-translational modifications[2]
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