| Literature DB >> 24462900 |
Nak Won Kim1, Min Sang Lee1, Kyu Ri Kim2, Jung Eun Lee1, Kyuri Lee1, Jong Sung Park1, Yoh Matsumoto3, Dong-Gyu Jo1, Haeshin Lee2, Doo Sung Lee4, Ji Hoon Jeong5.
Abstract
Microneedle (MN)-based DNA vaccines have many advantages over conventional vaccines administered by hypodermic needles. However, an efficient strategy for delivering DNA vaccines to intradermal cells has not yet been established. Here, we report a new approach for delivering polyplex-based DNA vaccines using MN arrays coated with a pH-responsive polyelectrolyte multilayer assembly (PMA). This approach enabled rapid release of polyplex upon application to the skin. In addition to the polyplex-releasing MNs, we attempted to further maximize the vaccination by developing a polymeric carrier that targeted resident antigen presenting cells (APCs) rich in the intradermal area, as well as a DNA vaccine encoding a secretable fusion protein containing amyloid beta monomer (Aβ1-42), an antigenic determinant. The resulting vaccination system was able to successfully induce a robust humoral immune response compared to conventional subcutaneous injection with hypodermal needles. In addition, antigen challenge after immunization elicited an immediate and strong recall immune response due to immunogenic memory. These results suggest the potential utility of MN-based polyplex delivery systems for enhanced DNA vaccination.Keywords: DNA vaccine; Gene delivery; Layer-by-layer assembly; Microneedle array; pH-responsive materials
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Year: 2014 PMID: 24462900 DOI: 10.1016/j.jconrel.2014.01.016
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776