In vivo molecular imaging analysis of a nasal vaccine that induces protective immunity against botulism in nonhuman primates

J Immunol. 2010 Nov 1;185(9):5436-43. doi: 10.4049/jimmunol.1001789. Epub 2010 Sep 29.

Abstract

Nasal administration is an effective route for a needle-free vaccine. However, nasally administered Ags have the potential to reach the CNS directly from the nasal cavity, thus raising safety concerns. In this study, we performed real-time quantitative tracking of a nasal vaccine candidate for botulism, which is a nontoxic subunit fragment of Clostridium botulinum type A neurotoxin (BoHc/A) effective in the induction of the toxin-neutralizing immune response, by using (18)F-labeled BoHc/A-positron-emission tomography, an in vivo molecular imaging method. This method provides results that are consistent with direct counting of [(18)F] radioactivity or the traditional [(111)In]-radiolabel method in dissected tissues of mice and nonhuman primates. We found no deposition of BoHc/A in the cerebrum or olfactory bulb after nasal administration of (18)F-labeled BoHc/A in both animals. We also established a real-time quantitative profile of elimination of this nasal vaccine candidate and demonstrated that it induces highly protective immunity against botulism in nonhuman primates. Our findings demonstrate the efficiency and safety of a nasal vaccine candidate against botulism in mice and nonhuman primates using in vivo molecular imaging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Bacterial Vaccines / administration & dosage*
  • Bacterial Vaccines / immunology
  • Bacterial Vaccines / pharmacokinetics*
  • Botulinum Toxins, Type A / immunology
  • Botulism / diagnostic imaging*
  • Botulism / immunology
  • Botulism / prevention & control*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fluorodeoxyglucose F18 / pharmacokinetics
  • Macaca fascicularis
  • Mice
  • Mice, Inbred BALB C
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals / pharmacokinetics

Substances

  • Bacterial Vaccines
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • Botulinum Toxins, Type A