ArticleFrontiers in immunology2026
Preparation of a multiepitope vaccine candidate for camel bocavirus and evaluation of its immunogenicity in a mouse model.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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15 authors.
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Abstract
Introduction: Dromedary camel bocavirus (DBoV) poses a threat to camel health, yet no vaccine is available. Methods: Using immunoinformatics, B-cell, CTL, and HTL epitopes from VP1/VP2 were predicted. Four multi-epitope constructs (DBoV-A1 to A4) were designed with different adjuvants and evaluated in silico; DBoV-A2 and A4 were expressed, purified, and tested in BALB/c mice. Results: DBoV-A2 and A4 showed strong in silico binding to TLR9 and stable molecular dynamics. In mice, both induced significant IgG, IgM, IgA responses, Th1/Th2 cytokine secretion, and CD4⁺ T cell expansion without organ toxicity. Discussion: The consistency between computational predictions and in vivo immunogenicity supports these constructs as promising DBoV vaccine candidates.
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