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. 2023 Mar 25;11(1):268–282. doi: 10.1016/j.gendis.2023.02.027

Table 2.

Viral vectors for CRISPR/Cas9 delivery system.

Delivery Packaging capacity Advantages Disadvantages
Lentivirus Approximately 10 kb High transduction efficiency; large cargo size; low immunogenicity; ability to transduce dividing and non-dividing cells in different tissues Non-specific DNA integration causes cancer risk; complex packaging structure
Adenovirus Approximately 8–10 kb Efficient delivery; large cargo size Inflammatory response
Adeno-associated virus Approximately 4.7 kb Multiple serotypes; low immunogenicity; ability to transduce dividing and non-dividing cells in different tissues Pre-existing neutralizing antibodies; long-term expression of Cas9 causes off-target effects