Predominant cell-mediated immunity in the oral mucosa: gene gun-based vaccination against infectious diseases

J Dermatol Sci. 2003 May;31(3):203-10. doi: 10.1016/s0923-1811(03)00027-6.

Abstract

Background: Direct immunization via epithelial surfaces has been considered for many vaccine approaches, including DNA vaccines. It remains to be determined, however, which body site is suitable for genetic vaccination.

Objective: To characterize the effects of the oral mucosa-mediated genetic vaccination, we compared antigen-specific immune responses of the oral mucosal DNA vaccine to the flank skin vaccination against influenza virus and malaria parasite.

Methods: DNA vaccines against the influenza A/WSN/33 (H1N1) hemagglutinin and the malaria Plasmodium berghei circumsporozoite protein were administered respectively three times at 3-week intervals into the oral mucosa, skin, or liver of hamsters. The effects of their vaccine were evaluated by antigen-specific antibody production and cell-mediated killing activity. Furthermore, the in vivo malaria challenge test was also performed after the vaccination.

Results: Significant specific antibody production was not observed in each case, but interferon-gamma production and cell-mediated killing activity were strongly induced in splenic lymphocytes from hamsters with the oral vaccination. The in vivo malaria challenge after the oral mucosal vaccination significantly delayed the blood-appearance day of the parasites in comparison with other immunization sites (P<0.05).

Conclusion: These results suggest that gene immunization via the oral mucosa may induce cell-mediated immunity more efficiently than via the skin or liver, and that the oral mucosa may be one of the most suitable tissues for gene gun-based DNA vaccination against infectious diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biolistics / methods*
  • Cricetinae
  • Enzyme-Linked Immunosorbent Assay
  • Hemagglutination Inhibition Tests
  • Humans
  • Immunity, Cellular*
  • Immunity, Mucosal*
  • Infections / immunology*
  • Influenza A virus / genetics*
  • Influenza Vaccines*
  • Malaria Vaccines*
  • Mesocricetus
  • Plasmodium berghei / genetics
  • T-Lymphocytes, Cytotoxic / immunology
  • Vaccines, DNA*

Substances

  • Influenza Vaccines
  • Malaria Vaccines
  • Vaccines, DNA