Clinical potential of electroporation for gene therapy and DNA vaccine delivery.

Lambricht, Laure;Lopes, Alessandra;Kos, Spela;Sersa, Gregor;Vandermeulen, Gaëlle;et.al.
(2016) Expert Opinion on Drug Delivery — Vol. 13, n° 2, p. 295-310 (2016)

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Authors
  • Lambricht, LaureUCLouvain
    Author
  • Lopes, AlessandraUCLouvain
    Author
  • Kos, Spela
    Author
  • Sersa, Gregor
    Author
  • Préat, VéroniqueUCLouvain
    Author
  • Vandermeulen, GaëlleUCLouvain
    Author
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Abstract
(en) INTRODUCTION: Electroporation allows efficient delivery of DNA into cells and tissues, thereby improving the expression of therapeutic or immunogenic proteins that are encoded by plasmid DNA. This simple and versatile method holds a great potential and could address unmet medical needs such as the prevention or treatment of many cancers or infectious diseases. AREAS COVERED: This review explores the electroporation mechanism and the parameters affecting its efficacy. An analysis of past and current clinical trials focused on DNA electroporation is presented. The pathologies addressed, the protocol used, the treatment outcome and the tolerability are highlighted. In addition, several of the possible optimization strategies for improving patient compliance and therapeutic efficacy are discussed such as plasmid design, use of genetic adjuvants for DNA vaccines, choice of appropriate delivery site and electrodes as well as pulse parameters. EXPERT OPINION: The growing number of clinical trials and the results already available underline the strong potential of DNA electroporation which combines both safety and efficiency. Nevertheless, it remains critical to further increase fundamental knowledge to refine future strategies, to develop concerted and common DNA electroporation protocols and to continue exploring new electroporation-based therapeutic options.
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Lambricht, L., Lopes, A., Kos, S., Sersa, G., Préat, V., & Vandermeulen, G. (2016). Clinical potential of electroporation for gene therapy and DNA vaccine delivery. Expert Opinion on Drug Delivery, 13(2), 295-310. https://doi.org/10.1517/17425247.2016.1121990 (Original work published 2016)