Optimisation of intradermal DNA electrotransfer for immunisation

Vandermeulen, Gaëlle;Staes, Edith;Vanderhaeghen, Marie-Lise;Bureau, Michel Francis;Préat, Véronique;et.al.
(2007) Journal of Controlled Release — Vol. 124, n° 1-2, p. 81-87 (2007)

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Authors
  • Vandermeulen, GaëlleUCLouvain
    Author
  • Staes, EdithUCLouvain
    Author
  • Vanderhaeghen, Marie-LiseUCLouvain
    Author
  • Bureau, Michel Francis
    Author
  • Préat, VéroniqueUCLouvain
    Author
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Abstract
The development of DNA vaccines requires appropriate delivery technologies. Electrotransfer is one of the most efficient methods of non-viral gene transfer. In the present study, intradermal DNA electrotransfer was first optimised. Strong effects of the injection method and the dose of DNA on luciferase expression were demonstrated. Pre-treatments were evaluated to enhance DNA diffusion in the skin but neither hyaluronidase injection nor iontophoresis improved efficiency of intradermal DNA electrotransfer. Then, DNA immunisation with a weakly immunogenic model antigen, luciferase, was investigated. After intradermal injection of the plasmid encoding luciferase, electrotransfer (HV 700 V/cm 100 micros, LV 200 V/cm 400 ms) was required to induce immune response. The response was Th1-shifted compared to immunisation with the luciferase recombinant protein. Finally, DNA electrotransfer in the skin, the muscle or the ear pinna was compared. Muscle DNA electrotransfer resulted in the highest luciferase expression and the best IgG response. Nevertheless electrotransfer into the skin, the muscle and the ear pinna all resulted in IFN-gamma secretion by luciferase-stimulated splenocytes suggesting that an efficient Th1 response was induced in all case.
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Citations

Vandermeulen, G., Staes, E., Vanderhaeghen, M.-L., Bureau, M. F., Scherman, D., & Préat, V. (2007). Optimisation of intradermal DNA electrotransfer for immunisation. Journal of Controlled Release, 124(1-2), 81-87. https://doi.org/10.1016/j.jconrel.2007.08.010 (Original work published 2007)