Skip to main content
. 2025 Sep 27;34(1):68–96. doi: 10.1016/j.ymthe.2025.09.041

Table 2.

General features of common viral vectors for nucleic acid therapeutic delivery

Viral vector Basic characteristics Advantages Limitations
Adenoviruses
  • ∼26- to 48-kb double-stranded DNA genome

  • non-enveloped

  • non-integrating

  • high capacity

  • transduction of both dividing and non-dividing cells

  • broad tropism

  • high immunogenicity (especially earlier generations)

  • preexisting immunity prevalent in general population

Lentiviruses
  • ∼9.7-kb single-stranded RNA genome

  • enveloped

  • integrating in nature, non-integrating versions available

  • low immunogenicity

  • integration allows stable gene expression

  • transduction of both dividing and non-dividing cells

  • broad tropism

  • risk of insertional mutagenesis

  • moderate capacity

Adeno-associated viruses
  • ∼4.7-kb single-stranded DNA genome

  • non-enveloped

  • non-integrating

  • low immunogenicity

  • minimal health risk as the wild-type virus is not known to cause disease

  • ease of cloning due to small genome

  • diffusion through dense tumor mass due to small size

  • transduction of both dividing and non-dividing cells

  • broad tropism

  • low capacity

  • requires complementary strand synthesis in host, hence delayed transgene expression, or double-stranded versions need to be generated

HSVs
  • ∼152-kb double-stranded DNA genome

  • enveloped

  • non-integrating

  • high capacity

  • transduction of both dividing and non-dividing cells

  • broad tropism, including neuronal tropism

  • health risk as the wild-type virus is highly dangerous