Liposomal cationic charge and antigen adsorption are important properties for the efficient deposition of antigen at the injection site and ability of the vaccine to induce a CMI response

Malou Henriksen-Lacey, Dennis Christensen, Vincent W Bramwell, Thomas Lindenstrøm, Else M. Agger, Peter Andersen, Yvonne Perrie

Research output: Contribution to journalArticle

Abstract

With respect to liposomes as delivery vehicles and adjuvants for vaccine antigens, the role of vesicle surface charge remains disputed. In the present study we investigate the influence of liposome surface charge and antigen-liposome interaction on the antigen depot effect at the site of injection (SOI). The presence of liposome and antigen in tissue at the SOI as well as the draining lymphatic tissue was quantified to analyse the lymphatic draining of the vaccine components. Furthermore investigations detailing cytokine production and T-cell antigen specificity were undertaken to investigate the relationship between depot effect and the ability of the vaccine to induce an immune response. Our results suggest that cationic charge is an important factor for the retention of the liposomal component at the SOI, and a moderate to high (>50%) level of antigen adsorption to the cationic vesicle surface was required for efficient antigen retention in the same tissue. Furthermore, neutral liposomes expressing poor levels of antigen retention were limited in their ability to mediate long term (14 days) antigen presentation to circulating antigen specific T-cells and to induce the Th1 and Th17 arms of the immune system, as compared to antigen adsorbing cationic liposomes. The neutral liposomes did however induce the production of IL-5 at levels comparable to those induced by cationic liposomes, indicating that neutral liposomes can induce a weak Th2 response.
Original languageEnglish
Pages (from-to)102-108
Number of pages7
JournalJournal of Controlled Release
Volume145
Issue number2
Early online date8 Apr 2010
DOIs
Publication statusPublished - 14 Jul 2010

Keywords

  • immunologic adjuvants
  • animals
  • antigen presentation
  • antigens
  • cations
  • female
  • cellular immunity
  • injections
  • liposomes
  • mice
  • inbred C57BL mice
  • transgenic mice
  • spleen
  • T-lymphocytes
  • vaccines

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