Development of a lipoplex-type mRNA carrier composed of an ionizable lipid with a vitamin E scaffold and the KALA peptide for use as an ex vivo dendritic cell-based cancer vaccine

J Control Release. 2019 Sep 28:310:36-46. doi: 10.1016/j.jconrel.2019.08.002. Epub 2019 Aug 3.

Abstract

A dendritic cells (DCs)-based vaccine (DC-vaccine) system is an attractive technology for eliciting antigen-specific immune responses that can protect subjects from infectious diseases and for curing various types of cancers. For the insertion of a foreign antigen to DCs, the transfection of an antigen-coding mRNA to the cells is a promising approach. In order to introduce an antigen, a carrier for mRNA transfection is required, since the mRNA molecule per se is unstable in serum-containing medium. We previously reported on an ionizable lipid-like material with vitamin E-scaffolds (ssPalmE) as a material for a lipid nanoparticle (LNP)-based carrier for nucleic acids. In the present study, we report on the development of a lipoplex-type mRNA carrier for use as a DC-vaccine by using a combination of an ssPalmE-LNP and an α-helical cationic peptide "KALA" (ssPalmE-KALA). The transfection of mRNAs complexed with the ssPalmE-KALA achieved a significantly higher protein expression and the production of proinflammatory cytokines from murine bone marrow derived DCs (BMDCs) in comparison with a lipoplex that was prepared with an ssPalm with fatty acid-scaffolds (myristic acid; ssPalmM-KALA). A cellular uptake process and a pH-responsive membrane-destabilization activity cannot explain the preferred protein expression and immune-stimulation caused by the ssPalmE-KALA. Proteomic analyses suggest that transfection with the ssPalmM-KALA stimulates a down-regulatory pathway of translation, while the transfection with the ssPalmE-KALA does not stimulate it. In the vaccination with the BMDCs that were preliminarily transfected with an ovalbumin (OVA)-encoding mRNA elicited the induction OVA specific cytotoxic T-lymphocyte activity in vivo. In parallel, the vaccination induced significant prophylactic anti-tumor effects against a model tumor that stably expressed the OVA protein. Based on the above findings, the ssPalmE-KALA appears to be a potent ex vivo DCs-based RNA vaccine platform.

Keywords: Cancer immunotherapy; Lipoplex; Proteomics; RNA vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cancer Vaccines / administration & dosage*
  • Cancer Vaccines / genetics
  • Cancer Vaccines / immunology
  • Cell-Penetrating Peptides / chemistry*
  • Cytokines / biosynthesis
  • Dendritic Cells / immunology*
  • Drug Carriers / chemistry*
  • Gene Expression
  • Lipids / chemistry*
  • Liposomes
  • Mice, Inbred C57BL
  • Ovalbumin / genetics
  • Ovalbumin / immunology
  • RNA, Messenger / administration & dosage*
  • RNA, Messenger / genetics
  • RNA, Messenger / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • Vitamin E / chemistry*

Substances

  • Cancer Vaccines
  • Cell-Penetrating Peptides
  • Cytokines
  • Drug Carriers
  • Lipids
  • Liposomes
  • RNA, Messenger
  • Vitamin E
  • Ovalbumin