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. Author manuscript; available in PMC: 2009 Jun 15.
Published in final edited form as: Curr Gene Ther. 2005 Dec;5(6):559–572. doi: 10.2174/156652305774964721

Table 3.

Advantages and Disadvantages of Viral Vectors for Gene Therapy

Vector Advantages Disadvantages

Enveloped
HSV/r Broad cell tropism, high tropism for neurons latency in neurons, very stable Expression of viral genes
Highly toxic
Transient transgene expression in cells other than neurons
HSV/a Broad cell tropism, high tropism for neurons latency in neurons, very stable No expression of viral genes
Large transgene capacity Lower toxicity
Retrovirus Persistent transgene expression Infects dividing cells only
Integration into host genome
Risk of insertion mutagenesis
Lentivirus Broad cell tropism Integration into host genome
Infection of dividing and non dividing cells Risk of insertion mutagenesis
Persistent transgene expression Risk of seroconversion

Non-enveloped
Rad Broad cell tropism, infection of dividing and non dividing cells Expression of viral proteins
High titer stocks, good yields Inflammatory and immune responses
Transient expression
RCA potential contamination
HD-Ad Broad cell tropism, infection of dividing and non dividing cells Difficulty in large scale production
Non expression of viral proteins Helper virus and RCA potential contamination
Lower inflammatory and cellular immune response
Longer term transgene expression
AAV Broad cell tropism Small insertion capacity
Infection of dividing and non dividing cells Integration into host genome
Non expression of viral proteins
Discrete immune response