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Nanoporous polyelectrolyte vaccine microcarriers. A formulation platform for enhancing humoral and cellular immune responses.
De Koker, Stefaan; Fierens, Kaat; Dierendonck, Marijke; De Rycke, Riet; Lambrecht, Bart N; Grooten, Johan; Remon, Jean Paul; De Geest, Bruno G.
Afiliação
  • De Koker S; Department of Pharmaceutics, Ghent University, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Zwijnaarde, Ghent, Belgium.
  • Fierens K; VIB Inflammation Research Center, University of Ghent, Ghent, Belgium; Department of Respiratory Medicine, University Hospital Ghent, Ghent, Belgium.
  • Dierendonck M; Department of Pharmaceutics, Ghent University, Ghent, Belgium.
  • De Rycke R; VIB Inflammation Research Center, University of Ghent, Ghent, Belgium; Department of Plant Systems Biology, VIB, and Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.
  • Lambrecht BN; VIB Inflammation Research Center, University of Ghent, Ghent, Belgium; Department of Respiratory Medicine, University Hospital Ghent, Ghent, Belgium.
  • Grooten J; Department of Biomedical Molecular Biology, Ghent University, Zwijnaarde, Ghent, Belgium.
  • Remon JP; Department of Pharmaceutics, Ghent University, Ghent, Belgium.
  • De Geest BG; Department of Pharmaceutics, Ghent University, Ghent, Belgium. Electronic address: br.degeest@ugent.be.
J Control Release ; 195: 99-109, 2014 Dec 10.
Article em En | MEDLINE | ID: mdl-25078552
ABSTRACT
In this paper we report on the design, characterization and immuno-biological evaluation of nanoporous polyelectrolyte microparticles as vaccine carrier. Relative to soluble antigen, formulation of antigen as a sub-10 µm particle can strongly enhance antigen-specific cellular immune responses. The latter is crucial to confer protective immunity against intracellular pathogens and for anti-cancer vaccines. However, a major bottleneck in microparticulate vaccine formulation is the development of generic strategies that afford antigen encapsulation under benign and scalable conditions. Our strategy is based on spray drying of a dilute aqueous solution of antigen, oppositely charged polyelectrolytes and mannitol as a pore-forming component. The obtained solid microparticles can be redispersed in aqueous medium, leading to leaching out of the mannitol, thereby creating a highly porous internal structure. This porous structure enhances enzymatic processing of encapsulated proteins. After optimizing the conditions to process these microparticles we demonstrate that they strongly enhance cross-presentation in vitro by dendritic cells to CD8 T cells. In vivo experiments in mice confirm that this vaccine formulation technology is capable of enhancing cellular immune responses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Portadores de Fármacos / Vacinas / Ovalbumina / Sulfato de Dextrana / Manitol Limite: Animals Idioma: En Revista: J Control Release Assunto da revista: FARMACOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Portadores de Fármacos / Vacinas / Ovalbumina / Sulfato de Dextrana / Manitol Limite: Animals Idioma: En Revista: J Control Release Assunto da revista: FARMACOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica