Table V.
Properties of the two existing animal vaccines against Rift Valley fever virus.
|
Live-attenuated vaccine |
Inactivated vaccine |
Origin/Production |
-
Derived from the Smithburn vaccine strain (origin = Uganda)
-
Attenuated by successive ICa passage in newborn mice and in embryonated eggs (resulting in a neurotropic strain); produced in cell culture since 1971
|
|
Advantages |
|
-
No adverse effects
-
No contraindications
|
Limitations |
-
May induce abortions and fœtal malformations → major contraindications for use in pregnant animals
-
Transient viraemia
-
Possible residual human pathogenicity
-
Possible reassortment with field wild–type virus strains
|
-
Need two injections during the first year and booster doses annually
-
Short duration of protective immunity (necessitating annual booster doses)
-
Expensive production costs
|
Recommendations for vaccine use |
|
|
Common properties |
-
Do not allow the differentiation of vaccinated and naturally-infected animals (i.e., no « DIVAb test » available)
-
Age of vaccination: > 6 month of age
|
b DIVA test = “Differentiation of infected and vaccinated animals”.