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. 2007 Dec 11;18(6):546–556. doi: 10.1016/j.copbio.2007.10.010

Table 1.

Key features of replicating and non-replicating vaccine vectors

Viral vector Type Insert Advantages Disadvantages
Adenovirus Non-replicating; ds DNA 7–8 kb Common features: Prior immunity to Ad5
Targets mucosal inductive sites High doses needed to elicit immunity
Infects dividing, non-dividing, and dendritic cells
No integration
Physically and genetically stable



Specific for non-replicating vector:
Safe
Long history of gene therapy use
Multiple serotypes and chimeric forms



Adenovirus Replicating ds DNA 3–4 kb Specific for replicating vector: Small insert size
Common features above Concern for intranasal administration
Low dose, mucosal delivery
Persistent immunity
Induction of immune modulators
Safe as an oral vaccine



Adeno-associated virus Non-replicating; ss DNA <5 kb Resistant to acid; physically stable Difficult production uses helper virus
Alternate serotypes available Possible integration
Tropic for dendritic cells Prior immunity to prevalent AAV2
Non-pathogenic



Alphavirus Non-replicating; +ss RNA <8 kb No integration Safety concerns regarding VEE
Does not elicit anti-vector immunity Difficult to produce
Targets dendritic cells
Highly immunogenic



Herpesvirus Non-replicating; ds DNA <50 kb Infects many cell types; targets mucosa Prior immunity
Durable immunity Lesser immunogenicity
Induces Th1 responses Difficult to manufacture



Measles virus Replicating; -ss RNA >5 kb Persistent immunity Prior immunity
Infects dendritic cells, macrophages
No integration; genetic stability



Poxviruses: Vaccinia Replicating; ds DNA >10 kb Excellent immunogenicity with history of eradicating smallpox Safety concerns in immune compromised
Poxviruses: NYVAC; MVA Non-replicating; ds DNA >10 kb Excellent immunogenicity; more immunogenic than avian poxviruses Prior immunity
Poxviruses: ALVAC; FPV Non-replicating; ds DNA >10 kb No prior immunity Less immunogenic than mammalian poxviruses



Vesicular stomatitis virus Replicating; -ss RNA >5 kb No integration; high level expression Safety; potentially neurovirulent
Ease of production Attenuated forms less immunogenic
No prior immunity
Mucosal administration