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Effectiveness of cholera toxin B subunit as an adjuvant for nasal influenza vaccination despite pre-existing immunity to CTB.

Abstract
In a previous paper, it was shown that cholera toxin B subunit (CTB) augments the production of protective antibodies to influenza virus when CTB is inoculated intranasally into Balb/c mice together with influenza HA vaccine. The present study was designed to determine whether the effectiveness of CTB as a potent adjuvant for nasal vaccination could be limited by pre-existing immunity to CTB. Mice were sensitized by intranasal inoculation of either 1 or 0.05 microgram of CTB 2, 4 and/or 6 weeks before nasal vaccination. They were then vaccinated by either a single inoculation of vaccine together with 1 microgram of CTB or a two-dose regimen, composed of a primary inoculation of vaccine together with 0.05 microgram of CTB and a subsequent inoculation of vaccine alone. Levels of nasal IgA antibodies to CTB increased with the increase of the dose of CTB and the frequency of CTB-inoculation. Pre-existing immunity to CTB, however, did not significantly reduce the levels of both nasal IgA and serum haemagglutination-inhibiting (HI) antibodies to influenza virus and did not change the ability of the vaccinated mice to resist viral challenge. These results suggest that a relatively low dose of CTB could be inoculated repeatedly into animals as an adjuvant for nasal vaccination.
AuthorsS Tamura, H Funato, T Nagamine, C Aizawa, T Kurata
JournalVaccine (Vaccine) Vol. 7 Issue 6 Pg. 503-5 (Dec 1989) ISSN: 0264-410X [Print] Netherlands
PMID2609726 (Publication Type: Journal Article)
Chemical References
  • Adjuvants, Immunologic
  • Antibodies, Viral
  • Immunoglobulin A
  • Influenza Vaccines
  • Peptide Fragments
  • Cholera Toxin
Topics
  • Adjuvants, Immunologic (pharmacology)
  • Administration, Intranasal
  • Animals
  • Antibodies, Viral (analysis)
  • Cholera Toxin (immunology, pharmacology)
  • Female
  • Immunoglobulin A (analysis)
  • Influenza Vaccines (administration & dosage, immunology)
  • Mice
  • Mice, Inbred BALB C
  • Peptide Fragments (pharmacology)

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