Controlled Delivery of Plasmid DNA to Melanoma Tumors by Gene Electrotransfer

Methods Mol Biol. 2021:2265:635-644. doi: 10.1007/978-1-0716-1205-7_43.

Abstract

Gene electrotransfer (GET) is a reliable and effective physical method for in vivo delivery of plasmid DNA (pDNA). Several preclinical and clinical studies have utilized GET to deliver plasmids encoding immune stimulating genes for treatment of melanoma and other tumor types. Intratumor delivery of plasmids encoding cytokines directly to tumors can induce not only a local immune response, but a systemic one as well. To obtain an effective immune response, it is critical to achieve the appropriate expression pattern of the delivered transgene. Expression pattern (levels and kinetics) can be modified by manipulating the electrotransfer parameters. These parameters include the tissue target and the electric pulse parameters of pulse width, electric field, and pulse number. We have found that to induce a robust immune response, we needed only low to moderately elevated expression levels compared to controls. When developing a therapeutic protocol, it is important to establish what expression profile will enable the appropriate response. In this chapter we describe how to determine the appropriate GET protocol to achieve the expression profile that can result in the desired clinical response.

Keywords: Cytokines; Electroporation; Expression profile; Gene therapy; Immunotherapy.

MeSH terms

  • Cell Line, Tumor
  • Electroporation*
  • Gene Transfer Techniques*
  • Humans
  • Melanoma* / genetics
  • Melanoma* / metabolism
  • Plasmids* / genetics
  • Plasmids* / pharmacology
  • Transgenes*