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Journal of Clinical Microbiology, April 2002, p. 1400-1405, Vol. 40, No. 4
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.4.1400-1405.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Department of Biochemistry and ImmunologyUFMG, 31270-901 Belo Horizonte,1 Laboratory of Immunopathology, CPqRRFIOCRUZ, 30190-002 Belo Horizonte,2 Department of Immunology, Microbiology and ParasitologyUFU, 38400-902 Uberlândia, MG,3 Fleury Laboratory, 01333-910 São Paulo, SP, Brazil4
Received 15 October 2001/ Returned for modification 5 December 2001/ Accepted 27 January 2002
In the present study we developed an enzyme-linked immunosorbent assay (ELISA) to measure immunoglobulin M (IgM) specific for glycoinositolphospholipids (GIPL) derived from tachyzoite membrane (IgM-GIPL ELISA). The sensitivity and specificity of the assay were compared with those of commercially available Toxoplasma-specific IgM serological tests, namely, immunofluorescence assay (IFA) with fixed tachyzoites and capture ELISA employing tachyzoite extracts. Our results show that all patients with acute toxoplasmosis, as determined by clinical data and conventional serological tests, were also positive by the IgM-GIPL ELISA. Interestingly, many patients that were classified as indeterminate, who had IgG with high avidity but positive results in the IgM-specific IFA and capture ELISA, were negative by the IgM-GIPL ELISA. Finally, we tested the sera from patients with rheumatoid arthritis and various parasitic infections and found no evidence of false positives in the IgM-GIPL ELISA.
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