Dual-route targeted vaccine protects efficiently against botulinum neurotoxin A complex

  • Bikash Sahay
  • , Natacha Colliou
  • , Mojgan Zadeh
  • , Yong Ge
  • , Minghao Gong
  • , Jennifer L. Owen
  • , Melissa Valletti
  • , Christian Jobin
  • , Mansour Mohamadzadeh

Producción científica: Articlerevisión exhaustiva

12 Citas (Scopus)

Resumen

Clostridium botulinum readily persists in the soil and secretes life-threatening botulinum neurotoxins (BoNTs) that are categorized into serotypes A to H, of which, serotype A (BoNT/A) is the most commonly occurring in nature. An efficacious vaccine with high longevity against BoNT intoxication is urgent. Herein, we developed a dual-route vaccine administered over four consecutive weeks by mucosal and parenteral routes, consisting of the heavy chain (Hc) of BoNT/A targeting dendritic cell peptide (DCpep) expressed by Lactobacillus acidophilus as a secretory immunogenic protein. The administered dual-route vaccine elicited robust and long-lasting memory B cell responses comprising germinal center (GC) B cells and follicular T cells (Tfh) that fully protected mice from lethal oral BoNT/A fatal intoxication. Additionally, passively transferring neutralizing antibodies against BoNT/A into naïve mice induced robust protection against BoNT/A lethal intoxication. Together, a targeted vaccine employing local and systemic administrative routes may represent a novel formulation eliciting protective B cell responses with remarkable longevity against threatening biologic agents such as BoNTs.

Idioma originalEnglish (US)
Páginas (desde-hasta)155-164
Número de páginas10
PublicaciónVaccine
Volumen36
N.º1
DOI
EstadoPublished - ene 2 2018
Publicado de forma externa

ASJC Scopus subject areas

  • Molecular Medicine
  • General Immunology and Microbiology
  • General Veterinary
  • Public Health, Environmental and Occupational Health
  • Infectious Diseases

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