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ABSTRACT: Background
Anthrax and smallpox are high-risk infectious diseases, and considered as potential agents for bioterrorism. To develop an effective countermeasure for these diseases, we constructed a bivalent vaccine against both anthrax and smallpox by integrating a gene encoding protective antigen (PA) of Bacillus anthracis to the genome of the attenuated vaccinia virus strain, KVAC103.Results
Immunization with this bivalent vaccine induced antibodies against both PA and vaccinia virus in a mouse model. We also observed that the efficacy of this vaccine can be enhanced by combined immunization with immunoadjuvant-expressing KVAC103. Mouse groups co-immunized with PA-expressing KVAC103 and either interleukin-15 (IL-15) or cholera toxin subunit A (CTA1)-expressing KVAC103 showed increased anti-PA IgG titer and survival rate against B. anthracis spore challenge compared to the group immunized with PA-expressing KVAC103 alone.Conclusions
We demonstrated that the attenuated smallpox vaccine KVAC103 is an available platform for a multivalent vaccine and co-immunization of immunoadjuvants can improve vaccine performance.
SUBMITTER: Park DB
PROVIDER: S-EPMC7938549 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature
Park Deok Bum DB Ahn Bo-Eun BE Son Hosun H Lee Young-Ran YR Kim Yu-Ri YR Jo Su Kyoung SK Chun Jeong-Hoon JH Yu Jae-Yon JY Choi Myung-Min MM Rhie Gi-Eun GE
BMC microbiology 20210308 1
<h4>Background</h4>Anthrax and smallpox are high-risk infectious diseases, and considered as potential agents for bioterrorism. To develop an effective countermeasure for these diseases, we constructed a bivalent vaccine against both anthrax and smallpox by integrating a gene encoding protective antigen (PA) of Bacillus anthracis to the genome of the attenuated vaccinia virus strain, KVAC103.<h4>Results</h4>Immunization with this bivalent vaccine induced antibodies against both PA and vaccinia v ...[more]