Skip to main content
. 2017 Jun 8;18(6):1231. doi: 10.3390/ijms18061231

Table 1.

Main viral vector and their characteristics used in pre-clinical and clinical strategies of gene therapy for pancreatic cancer.

Virus Insertion Capacity Target Cells Delivery Transgene Expression Level of Expression Pre-existant Immunity Bio-Safety
AdV 35 kb Dividing or non dividing Ex vivo or In situ Transient High Yes Immunogenic, inflammation No integration
AAV 4.8 kb Dividing or non dividing Ex vivo or In situ Stable Moderate Yes Mutational integration
Retrov 8 kb Dividing Ex vivo or In situ Stable Moderate No Mutational integration
LentiV 10 kb Dividing or non dividing Ex vivo or In situ Stable High No Mutational integration, recombination with WT HIV
HSV 30 kb Dividing or non dividing Ex vivo or In situ Transient High Yes Mutational integration, neurotoxicity
Pox 25 kb Dividing or non dividing In vivo or In situ Stable High No Immunogenic, Adjuvant to vaccination
SV40 5 kb Dividing or non dividing Ex vivo or In situ Stable Moderate No Mutational integration

AdV: adenovirus derived vector; AAV: Adeno-associated derived vector; RetroV: retroviral derived vector; LentiV: lentiviral derived vector; HSV: herpes simplex viros derived vector; Pox: Pox and vaccinia virus derived vector; SV40: simian virus 40 (papova virus). AdV, HSV and Pox are double stranded DNA virus; AAV is a single stranded DNA virus; RetroV and LentiV are single stranded RNA virus. WT: wild type.