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Optimisation of a lipid based oral delivery system containing A/Panama influenza haemagglutinin
Ist Teil von
Vaccine, 2004-06, Vol.22 (19), p.2425-2429
Ort / Verlag
Oxford: Elsevier Ltd
Erscheinungsjahr
2004
Quelle
MEDLINE
Beschreibungen/Notizen
Vaccine antigens administered by the oral route are often degraded by gastric secretions during gastrointestinal transit. This necessitates larger and more frequent doses of antigen for vaccination. A delivery system, which overcomes this, is a lipid vesicle containing bile salts (bilosome), which prevents antigen degradation and enhances mucosal penetration. The effect of bilosome formulation modification on vaccine transit efficacy across the mucosa was determined. Specific antibody levels were assessed by end-point titre ELISA and the subclasses determined. Significant IgG1 titres were induced when the protein loading was doubled from 15 to 30
μg (
P=0.009) and was equivalent to antigen administration by the subcutaneous route. No IgG2a was induced, indicating the generation of a T
H2 response. Significant mucosal IgA levels were also observed with this treatment group (
P=0.05).