Key result
35-antigen adenovirus-vectored cocktail fails to protect wild boar against virulent ASFV challenge.
Why the study?
African swine fever lacks an effective vaccine, and prior subunit prototypes combining fewer antigens (between 2 and 22) failed to elicit protective efficacy.
Does immunization with a cocktail of thirty-five adenovirus-vectored ASFV antigens prevent African Swine Fever in wild boar?
Does immunization with a cocktail of thirty-five adenovirus-vectored ASFV antigens prevent African Swine Fever in wild boar?
Absolute Event Rate: 100% vs 100%
A cocktail of 35 adenovirus-vectored ASFV antigens failed to protect wild boar against virulent African Swine Fever Virus challenge.
Adenovirus-vectored ASFV antigen cocktail failed to protect wild boar; leaves open alternative vaccine strategies against virulent isolates.
African swine fever (ASF) is a viral disease of domestic and wild suids for which there is currently no vaccine or treatment available. The recent spread of ASF virus (ASFV) through Europe and Asia is causing enormous economic and animal losses. Unfortunately, the measures taken so far are insufficient and an effective vaccine against ASFV needs to be urgently developed. We hypothesized that immunization with a cocktail of thirty-five rationally selected antigens would improve the protective efficacy of subunit vaccine prototypes given that the combination of fewer immunogenic antigens (between 2 and 22) has failed to elicit protective efficacy. To this end, immunogenicity and efficacy of thirty-five adenovirus-vectored ASFV antigens were evaluated in wild boar. The treated animals were divided into different groups to test the use of BioMize adjuvant and different inoculation strategies. Forty-eight days after priming, the nine treated and two control wild boar were challenged with the virulent ASFV Arm07 isolate. All animals showed clinical signs and pathological findings consistent with ASF. This lack of protection is in line with other studies with subunit vaccine prototypes, demonstrating that there is still much room for improvement to obtain an effective subunit ASFV vaccine.
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Cadenas-Fernández et al. (2020) studied African swine fever (n=11). Adenovirus-vectored African Swine Fever Virus Antigens Cocktail vs. Control was evaluated on Clinical signs and pathological findings consistent with ASF. Immunization with a cocktail of thirty-five adenovirus-vectored ASFV antigens failed to protect wild boar against the virulent ASFV Arm07 isolate, with 100% of animals developing clinical signs.
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