Table 2

Comparison of the properties of the major DNA (top) and RNA (bottom) viruses used for development of oncolytic virotherapy platforms

DNA virusesVaccinia virusAdenovirusHerpesvirusParvovirus H1
Natural hostHuman (v)HumanHumanRat
GenomedsDNAdsDNAdsDNAssDNA
Replication siteCNNN
Nuclear integration+++
Cell receptorNot neededCARHVEM/nectinSialic acid residues
Transgene capacity++++++++
Deliveryi.t and i.vi.ti.ti.t and i.v
Hypoxia++n.k
Pre-existing immunity+++++++
Antiviral drugs available+++
RNA virusesReovirusCoxsackievirusPoliovirusMeasles virusNDVVSV
Natural hostHumanHumanHuman (v)Human (v)BirdHuman
GenomedsRNAssRNAssRNAssRNAssRNAssRNA
Replication siteCCCCCC
Nuclear integration
Cell receptorUnknownCAR/ICAM/DAFCD155SLAM/CD46UnknownLDLR
Transgene capacity+++
Deliveryi.t/i.vi.t/i.vi.ti.ti.t/i.vi.t/i.v
Hypoxian.k+n.k+n.k
Pre-existing immunity++++++++++
Antivirals
  • C, cytoplasmic replication; CAR, coxsackie-adenovirus receptor; DAF, decay accelerating factor; dsDNA, double-stranded DNA; dsRNA, double-stranded RNA; HVEM, herpesvirus entry mediator; ICAM, intercellular adhesion molecule; i.t, intratumoral; i.v, intravenous; LDLR, low density lipoprotein receptor; N, nuclear replication; N, nuclear replication; NDV, Newcastle disease virus; n.k, not known; ssDNA, single-stranded DNA; ssRNA, single-stranded RNA; v, vaccine strain; VSV, vesicular stomatitis virus.