Abstract
Intranasal administration of vaccines is preferred for induction of mucosal immune responses. In this study, mice were immunised intranasally and subcutaneously with influenza-immuno stimulating complexes (influenza-ISCOM). The intranasal dose was 15-times the subcutaneous dose. All mice dosed with influenza-ISCOMs survived challenge with live virus and comparable serum antibody and splenic cytotoxic T-lymphocyte responses were detected in both groups. Induction of mucosal IgA was significantly higher with intranasal immunisation and was comparable to responses induced with the heat labile enterotoxin of Escherichia coli as adjuvant. These findings demonstrate that intranasal administration of high dose influenza-ISCOM results in potent systemic and mucosal immune responses.
MeSH terms
-
Adjuvants, Immunologic / administration & dosage
-
Administration, Intranasal
-
Animals
-
Antibodies, Viral / biosynthesis
-
Antibodies, Viral / blood
-
Bacterial Toxins / administration & dosage
-
Enterotoxins / administration & dosage
-
Escherichia coli Proteins*
-
Humans
-
ISCOMs / administration & dosage*
-
Immunity, Mucosal
-
Immunoglobulin A, Secretory / biosynthesis
-
Influenza Vaccines / administration & dosage*
-
Influenza, Human / immunology
-
Influenza, Human / prevention & control
-
Injections, Subcutaneous
-
Mice
-
Mice, Inbred BALB C
-
Orthomyxoviridae / immunology
-
T-Lymphocytes, Cytotoxic / immunology
Substances
-
Adjuvants, Immunologic
-
Antibodies, Viral
-
Bacterial Toxins
-
Enterotoxins
-
Escherichia coli Proteins
-
ISCOMs
-
Immunoglobulin A, Secretory
-
Influenza Vaccines
-
heat-labile enterotoxin, E coli