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Single dose of DPX-rPA, an enhanced-delivery anthrax vaccine formulation, protects against a lethal Bacillus anthracis spore inhalation challenge.
Weir, Genevieve M; MacDonald, Lisa D; Rajagopalan, Rajkannan; Sivko, Gloria S; Valderas, Michelle W; Rayner, Jonathan; Berger, Bradley J; Sammatur, Leeladhar; Stanford, Marianne M.
Afiliación
  • Weir GM; IMV Inc., 130 Eileen Stubbs Avenue, Suite 19, Dartmouth, NS B3B 2C4 Canada.
  • MacDonald LD; IMV Inc., 130 Eileen Stubbs Avenue, Suite 19, Dartmouth, NS B3B 2C4 Canada.
  • Rajagopalan R; IMV Inc., 130 Eileen Stubbs Avenue, Suite 19, Dartmouth, NS B3B 2C4 Canada.
  • Sivko GS; 2Battelle, 1425 Plain City Georgesville Road, West Jefferson, OH 43162 USA.
  • Valderas MW; 3Southern Research, 2000 9th Avenue S, Birmingham, AL 35205 USA.
  • Rayner J; 3Southern Research, 2000 9th Avenue S, Birmingham, AL 35205 USA.
  • Berger BJ; 4Suffield Research Centre, Defence Research and Development Canada, Medicine Hat, AB T1A 8K6 Canada.
  • Sammatur L; IMV Inc., 130 Eileen Stubbs Avenue, Suite 19, Dartmouth, NS B3B 2C4 Canada.
  • Stanford MM; IMV Inc., 130 Eileen Stubbs Avenue, Suite 19, Dartmouth, NS B3B 2C4 Canada.
NPJ Vaccines ; 4: 6, 2019.
Article en En | MEDLINE | ID: mdl-30774997
ABSTRACT
Anthrax is a serious biological threat caused by pulmonary exposure to aerosolized spores of Bacillus anthracis. Biothrax® (anthrax vaccine adsorbed (AVA)) is the only Food and Drug Administration-licensed vaccine and requires five administrations over 12 months with annual boosting to maintain pre-exposure prophylaxis. Here we report the evaluation of a single intramuscular injection of recombinant B. anthracis-protective antigen (rPA) formulated in the DPX delivery platform. Immune responses were compared to an alum-based formulation in mice and rabbits. Serological analysis of anti-rPA immunoglobulin G and toxin neutralization activity demonstrated higher responses induced by DPX-rPA when compared to rPA in alum. DPX-rPA was compared to AVA in rabbits and non-human primates (NHPs). In both species, DPX-rPA generated responses after a single immunization, whereas AVA required two immunizations. In rabbits, single injection of DPX-rPA or two injections of AVA conferred 100% protection from anthrax challenge. In NHPs, single-dose DPX-rPA was 100% protective against challenge, whereas one animal in the two-dose AVA group and all saline administered animals succumbed to infection. DPX-rPA was minimally reactogenic in all species tested. These data indicate that DPX-rPA may offer improvement over AVA by reducing the doses needed for protective immune responses and is a promising candidate as a new-generation anthrax vaccine.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: NPJ Vaccines Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: NPJ Vaccines Año: 2019 Tipo del documento: Article