Polyplex-releasing microneedles for enhanced cutaneous delivery of DNA vaccine

J Control Release. 2014 Apr 10:179:11-7. doi: 10.1016/j.jconrel.2014.01.016. Epub 2014 Jan 23.

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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / administration & dosage*
  • Amyloid beta-Peptides / genetics
  • Amyloid beta-Peptides / immunology
  • Animals
  • Antibodies / blood
  • Antigen-Presenting Cells / drug effects
  • Antigen-Presenting Cells / immunology
  • Equipment Design
  • Female
  • Gene Transfer Techniques / instrumentation*
  • Hydrogen-Ion Concentration
  • Immunity, Humoral
  • Immunization*
  • Immunologic Memory
  • Injections, Subcutaneous
  • Mice
  • Mice, Inbred BALB C
  • Miniaturization
  • Needles
  • Peptide Fragments / administration & dosage*
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology
  • Polymers / chemistry*
  • Skin / drug effects
  • Skin / immunology
  • Time Factors
  • Vaccines, DNA / administration & dosage*
  • Vaccines, DNA / genetics
  • Vaccines, DNA / immunology

Substances

  • Amyloid beta-Peptides
  • Antibodies
  • Peptide Fragments
  • Polymers
  • Vaccines, DNA
  • amyloid beta-protein (1-42)