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A novel adjuvanted capsule based strategy for oral vaccination against infectious diarrhoeal pathogens.
Davitt, Christopher J H; McNeela, Edel A; Longet, Stephanie; Tobias, Joshua; Aversa, Vincenzo; McEntee, Craig P; Rosa, Monica; Coulter, Ivan S; Holmgren, Jan; Lavelle, Ed C.
Afiliação
  • Davitt CJ; Adjuvant Research Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 PN40, Ireland.
  • McNeela EA; Adjuvant Research Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 PN40, Ireland.
  • Longet S; Adjuvant Research Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 PN40, Ireland.
  • Tobias J; University of Gothenburg Vaccine Research Institute (GUVAX), Dept. of Microbiology and Immunology, University of Gothenburg, Box 435, 405 30 Gothenburg, Sweden.
  • Aversa V; Sigmoid Pharma Limited, Dublin City University, The Invent Centre, DCU, Glasnevin, Dublin 9, Ireland.
  • McEntee CP; Adjuvant Research Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 PN40, Ireland.
  • Rosa M; Sigmoid Pharma Limited, Dublin City University, The Invent Centre, DCU, Glasnevin, Dublin 9, Ireland.
  • Coulter IS; Sigmoid Pharma Limited, Dublin City University, The Invent Centre, DCU, Glasnevin, Dublin 9, Ireland.
  • Holmgren J; University of Gothenburg Vaccine Research Institute (GUVAX), Dept. of Microbiology and Immunology, University of Gothenburg, Box 435, 405 30 Gothenburg, Sweden.
  • Lavelle EC; Adjuvant Research Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, D02 PN40, Ireland; Centre for Research on Adaptive Nanostructures and Nanodevices (CRANN); Advanced Materials Bio-Engineering Research Centre (AMBER), Trinity Coll
J Control Release ; 233: 162-73, 2016 07 10.
Article em En | MEDLINE | ID: mdl-27157995
ABSTRACT
Diarrhoeal infections are a major cause of morbidity and mortality with enterotoxigenic Escherichia coli (ETEC) and cholera imposing a significant global burden. There is currently no licensed vaccine for ETEC. Development of new nonliving oral vaccines has proven difficult due to the physicochemical and immunological challenges associated with the oral route. This demands innovative delivery solutions to protect antigens, control their release and build in immune-stimulatory activity. We describe the Single Multiple Pill® (SmPill®) vaccine formulation which combines the benefits of enteric polymer coating to protect against low gastric pH, a dispersed phase to control release and aid the solubility of non-polar components and an optimized combination of adjuvant and antigen to promote mucosal immunity. We demonstrate the effectiveness of this system with whole cell killed E. coli overexpressing colonization factor antigen I (CFA/I), JT-49. Alpha-galactosylceramide was identified as a potent adjuvant within SmPill® that enhanced the immunogenicity of JT-49. The bacteria associated with the dispersed phase were retained within the capsules at gastric pH but released at intestinal pH. Vaccination with an optimized SmPill® formulation promoted CFA/I-specific immunoglobulin A (IgA) responses in the intestinal mucosa in addition to serum IgG and a solubilized adjuvant was indispensable for efficacy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adjuvantes Imunológicos / Vacinas contra Escherichia coli / Proteínas de Fímbrias / Galactosilceramidas / Antígenos de Bactérias Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adjuvantes Imunológicos / Vacinas contra Escherichia coli / Proteínas de Fímbrias / Galactosilceramidas / Antígenos de Bactérias Idioma: En Ano de publicação: 2016 Tipo de documento: Article