Article ID Journal Published Year Pages File Type
1425627 Journal of Controlled Release 2010 7 Pages PDF
Abstract

HSV-2-gD2 DNA vaccine was precisely delivered to immunologically sensitive regions of the skin epithelia using dry-coated microprojection arrays. These arrays delivered a vaccine payload to the epidermis and the upper dermis of mouse skin. Immunomicroscopy results showed that, in 43 ± 5% of microprojection delivery sites, the DNA vaccine was delivered to contact with professional antigen presenting cells in the epidermal layer. Associated with this efficient delivery of the vaccine into the vicinity of the professional antigen presenting cells, we achieved superior antibody responses and statistically equal protection rate against an HSV-2 virus challenge, when compared with the mice immunized with intramuscular injection using needle and syringe, but with less than 1/10th of the delivered antigen.

Graphical abstractThrough skin-targeted delivery of HSV-2-gD2 DNA vaccine in mouse model, we achieved superior antibody responses and statistically equal protection rate against an HSV-2 virus challenge, when compared with the mice immunized with intramuscular injection using needle and syringe — but with less than 1/10th of the delivered antigen.Figure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Materials Science Biomaterials
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