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Soluble extracts from larval Ostertagia ostertagi modulating immune function.

D A Cross, P H Klesius

    International Journal for Parasitology
    |February 1, 1989
    PubMed
    Summary

    A specific Ostertagia ostertagi antigen suppressed antibody production and B cell activity in mice. This immune-suppressive antigen also reduced lymphocyte responses to Concanavalin A stimulation.

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    Area of Science:

    • Immunology
    • Parasitology
    • Veterinary Science

    Background:

    • Ostertagia ostertagi is a significant gastrointestinal nematode parasite affecting livestock.
    • Understanding host immune responses to parasitic antigens is crucial for developing effective control strategies.
    • Immune modulation by parasite antigens can impact host susceptibility and vaccine efficacy.

    Purpose of the Study:

    • To investigate the immunomodulatory effects of Ostertagia ostertagi larval antigens on antibody production and lymphocyte function in BALB/c mice.
    • To identify specific antigens responsible for immune suppression.
    • To evaluate the impact of these antigens on B cell activity and T cell proliferation.

    Main Methods:

    • BALB/c mice were immunized with O. ostertagi antigens and T-dependent antigens (KLH or SR).

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  • Antibody production was assessed using enzyme-linked immunosorbent assay (ELISA).
  • B cell activity was measured by modified Jerne plaque assay, and lymphocyte blastogenesis was evaluated using Concanavalin A stimulation in vitro.
  • Main Results:

    • A semi-purified larval antigen significantly decreased anti-keyhole limpet hemocyanin (KLH) serum antibody levels.
    • The same antigen reduced the number of anti-sheep erythrocytes (SR) IgM-secreting B cells.
    • This antigen suppressed lymphocyte blastogenesis in cultured splenic lymphocytes stimulated with Concanavalin A.

    Conclusions:

    • Certain Ostertagia ostertagi larval antigens possess immunomodulatory properties that can suppress host antibody production and B cell function.
    • These antigens may interfere with T cell activation, as indicated by reduced lymphocyte blastogenesis.
    • Further research into these immunosuppressive antigens could inform vaccine development and parasite control strategies.