Use of a monoclonal antibody in a double-sandwich ELISA for detection of IgM antibodies to Toxoplasma gondii major surface protein (P30) |
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Authors: | J Y Cesbron A Capron G Ovlaque F Santoro |
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Affiliation: | Centre d''Immunologie et de Biologie Parasitaire, Unité Mixte INSERM U 167 - CNRS 624, Institut Pasteur, B.P. 245, 59019 Lille Cédex, France |
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Abstract: | A double-sandwich ELISA, developed for detection of IgM antibodies to the major surface protein of Toxoplasma gondii (P30), is proposed for the diagnosis of acute acquired toxoplasmosis. The method is based on the capture of serum IgM antibodies, which are revealed indirectly by the sequential addition of a Toxoplasma extract and a beta-galactosidase-conjugated anti-P30 monoclonal antibody. All 57 patients tested with serological characteristics of recently acquired toxoplasmosis showed high levels of IgM anti-P30 antibodies. In addition, 5 out of the 24 patients with chronic toxoplasmosis and all 7 patients with a clinical acute infection in which the classical IgM serology was negative, also presented significant anti-P30 IgM antibodies. Patients with either rheumatoid factor or antinuclear antibodies were all negative. In view of its simplicity, specificity and sensitivity, this method is recommended for the current diagnosis of T. gondii infection. |
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Keywords: | monoclonal antibody ELISA IgM antibodies acute acquired toxoplasmosis serodiagnosis ELISA enzyme-linked immunosorbent assay mAb monoclonal antibodies P30 PBS phosphate-buffered saline |
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