Abstract
An ELISA containing a purified flagellar antigen from Borrelia burgdorferi (FLA-ELISA) was evaluated. The FLA-ELISA, detecting IgM and IgG together, did not have adequate specificity by itself. Good accuracy was obtained, however, when the FLA-ELISA was the first step in a two-step protocol that used immunoblotting as a conditional second test. Samples that scored positive or equivocal by the FLA-ELISA were evaluated with separate IgM and IgG immunoblots. The sensitivity of the two-step process for patients with erythema migrans or with later manifestations of Lyme disease was 64% and 100%, respectively. The specificity for healthy blood donors was 100% and was 90% for the aggregate of all persons with illnesses that may cause serologic cross-reactivity (98% if the samples from relapsing fever patients were excluded). Test precision was 96% overall, 99% for Lyme disease case serum samples, 100% for specimens from blood donors, and 88% for samples from persons with other illnesses.
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CITATION STYLE
Johnson, B. J. B., Robbins, K. E., Bailey, R. E., Cao, B. L., Sviat, S. L., Craven, R. B., … Dennis, D. T. (1996). Serodiagnosis of lyme disease: Accuracy of a two-step approach using a flagella-based ELISA and immunoblotting. Journal of Infectious Diseases, 174(2), 346–353. https://doi.org/10.1093/infdis/174.2.346
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