QuilA-adjuvanted T. gondii lysate antigens trigger robust antibody and IFN gamma(+) T cell responses in pigs leading to reduction in parasite DNA in tissues upon challenge infection

Mizanur Rahman, Bert Devriendt, Ignacio Gisbert Algaba, Bavo Verhaegen, Pierre Dorny, Katelijne Dierick, Eric Cox

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    Abstract

    Toxoplasma gondii is an intracellular parasite of all mammals and birds, responsible for toxoplasmosis. In healthy individuals T. gondii infections mostly remain asymptomatic, however this parasite causes severe morbidity and mortality in immunocompromised patients and congenital toxoplasmosis in pregnant women. The consumption of raw or undercooked pork is considered as an important risk factor to develop toxoplasmosis in humans. Since effective therapeutic interventions to treat toxoplasmosis are scarce, vaccination of meat producing animals may prevent T. gondii transmission to humans. Here, we evaluated the elicited immune responses and the efficacy of a potential vaccine candidate, generated by size fractionation of T. gondii lysate proteins, to reduce the parasite burden in tissues from experimentally T. gondii infected pigs as compared to vaccination with total lysate antigens (TLA). Our results show that both the vaccine candidate and the TLA immunization elicited strong serum IgG responses and elevated percentages of CD4 +CD8 +IFNγ + T cells in T. gondii infected pigs. However, the TLA vaccine induced the strongest immune response and reduced the parasite DNA load below the detection limit in brain and skeletal muscle tissue in most animals. These findings might inform the development of novel vaccines to prevent T. gondii infections in livestock species and humans.

    Original languageEnglish
    Article number2223
    JournalFrontiers in Immunology
    Volume10
    Number of pages12
    ISSN1664-3224
    DOIs
    Publication statusPublished - 2019

    Keywords

    • Toxoplasma gondii
    • pigs
    • TLA vaccine
    • QuilA
    • magnetic capture-qPCR
    • TOXOPLASMA-GONDII
    • VACCINE
    • SURVIVAL
    • IMMUNITY

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