1966
DOI: 10.4269/ajtmh.1966.15.149
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Comparison of the Indirect Fluorescent Antibody Test and Methylene Blue Dye Test for Detection of Antibodies to Toxoplasma Gondii

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Cited by 83 publications
(28 citation statements)
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“…Certain serologic methods are of little help in diagnosing congenital toxoplasmosis. This is especially true for some CF or IHA tests [606]. Results with these tests may be weakly positive or even negative in a newborn with congenital toxoplasmosis, and in the infant's mother.…”
Section: Demonstration Of Antibodies In Serum and Body Fluidsmentioning
confidence: 95%
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“…Certain serologic methods are of little help in diagnosing congenital toxoplasmosis. This is especially true for some CF or IHA tests [606]. Results with these tests may be weakly positive or even negative in a newborn with congenital toxoplasmosis, and in the infant's mother.…”
Section: Demonstration Of Antibodies In Serum and Body Fluidsmentioning
confidence: 95%
“…A positive reaction is detected by the bright yellow-green fluorescence of the organisms seen on examination by fluorescence microscopy. In general, qualitative agreement with the dye test and IFA test has been excellent [606]. Despite the claims of many workers, reliable and reproducible quantitative titers frequently are difficult to obtain.…”
Section: Sabin-feldman Dyementioning
confidence: 98%
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“…The serum samples were supplied by members of the NRCT network, and the presence of IgG or IgM antibodies was confirmed based on the results of the reference technique using at least two different methods for each antibody isotype, namely, the indirect immunofluorescence assay (IFAT-G) (19) and dye test (20)(21)(22) for IgG detection, and IFAT-M and immunosorbent agglutination assay (ISAGA-M; bioMérieux SA, Marcy-l'Etoile, France) (23) for IgM detection. IgA levels were not assessed.…”
Section: Samplesmentioning
confidence: 99%
“…If the clinical situation suggests toxoplasmosis, a fourfold rise in antibody titers, or even stable SabinFeldman or IgG-IFA titers of 1: 1,000 or greater or IgM-IFA titers of 1: 10 or greater, is compatible with the diagnosis. Problems in interpretation arise from the high prevalence of anti-Toxoplasma antibodies in the general population {22) or from missing the diagnostic fourfold rise in titers by the time the first sample is drawn [60]. The latter consideration has led investigators to suggest obtaining baseline serological studies in patients at risk [21}.…”
Section: Focal Brain Abnormalitiesmentioning
confidence: 99%