Progress and challenges associated with the development of ricin toxin subunit vaccines

Expert Rev Vaccines. 2016 Sep;15(9):1213-22. doi: 10.1586/14760584.2016.1168701. Epub 2016 Apr 6.

Abstract

The past several years have seen major advances in the development of a safe and efficacious ricin toxin vaccine, including the completion of two Phase I clinical trials with two different recombinant A subunit (RTA)-based vaccines: RiVax™ and RVEc™ adsorbed to aluminum salt adjuvant, as well as a non-human primate study demonstrating that parenteral immunization with RiVax elicits a serum antibody response that was sufficient to protect against a lethal dose aerosolized ricin exposure. One of the major obstacles moving forward is assessing vaccine efficacy in humans, when neither ricin-specific serum IgG endpoint titers nor toxin-neutralizing antibody levels are accepted as definitive predictors of protective immunity. In this review we summarize ongoing efforts to leverage recent advances in our understanding of RTA-antibody interactions at the structural level to develop novel assays to predict vaccine efficacy in humans.

Keywords: Toxin; antibody; biodefense; epitope; neutralizing; protection; vaccine.

Publication types

  • Review
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Chemical Warfare Agents / toxicity*
  • Clinical Trials, Phase I as Topic
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Humans
  • Poisoning / prevention & control*
  • Ricin / toxicity*
  • Vaccines, Subunit / immunology*
  • Vaccines, Subunit / isolation & purification*

Substances

  • Chemical Warfare Agents
  • Vaccines, Subunit
  • Ricin