In Algeria, Androctonus australis hector
scorpion envenomation remains a major problem of public health because of non-efficient
therapy. The development of safe
vaccine against
scorpion venom could be one key strategy for the envenomation prevention. The irradiation of
venom by γ-rays develops suitable immunogens which produced effective
antivenom and safe
vaccine. In this study, we investigated the ability of the irradiated toxic fraction (γ-FtoxG50) to induce long-term memory humoral response in immunized animals (mice and rabbits), by involving the long-lived plasma cells to prevent efficiently the lethality of
scorpion envenomation. For this purpose, an appropriate immunization schedule was established in mice and rabbits using three (3) similar doses of γ-FtoxG50 associated with
Alum adjuvant. Obtained results indicate that the long-term immunogenicity of γ-FtoxG50 is able to induce the long-term memory humoral response with a high level of specific
antibodies. The long-term persistence of antibody levels could depend on bone marrow memory plasma cells. These cells produce continuously
antibodies without
antigen stimulus. Furthermore, an enhanced memory response was obtained post-repeated envenomation with toxic native
venom that leads to improved protection of animals. Together, pre-existing protective
antibodies and the activation of memory B-cells could induce a rapid neutralization of
scorpion toxins and long-term protection against
scorpion envenomation.