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dc.contributor.authorDuVall, Adam S
dc.contributor.authorFairley, Jessica K
dc.contributor.authorSutherland, Laura
dc.contributor.authorBustinduy, Amaya L
dc.contributor.authorMungai, Peter L
dc.contributor.authorMuchiri, Eric M
dc.contributor.authorMalhotra, Indu
dc.contributor.authorKitron, Uriel
dc.contributor.authorKing, Charles H
dc.date.accessioned2018-09-05T06:44:43Z
dc.date.accessioned2020-02-07T09:19:57Z
dc.date.available2018-09-05T06:44:43Z
dc.date.available2020-02-07T09:19:57Z
dc.date.issued2014
dc.identifier.urihttp://repository.must.ac.ke/handle/123456789/1334
dc.description.abstractTo better delineate the impact of parasitic coinfection in coastal Kenya, we developed a novel specimen-sparing bead assay using multiplex flow immunoassay (MFI) technology to simultaneously measure serum or plasma immunoglobulin G4 (IgG4) against Brugia malayi antigen (BMA) and Schistosoma haematobium soluble worm antigen (SWAP). Properties of the bead assay were estimated by latent class analysis using data from S. haematobium egg counts/ filarial rapid diagnostic cards (RDTs), parasite-specific enzyme-linked immunosorbent assays (ELISAs), and the multichannel IgG4 assay. For schistosomiasis, the bead assay had an estimated sensitivity of 81% and a specificity of 45%, and it was more sensitive than ELISA or urine egg counts for diagnosing infection. For filariasis, it had a sensitivity of 86% and a specificity of 39%, and it was more sensitive than ELISA or RDT. Measuring antibody by MFI is feasible and may provide more accurate epidemiological information than current parasitological tests, especially in the setting of low-intensity infections.en_US
dc.language.isoenen_US
dc.publisherThe American Society of Tropical Medicine and Hygieneen_US
dc.subjectParasitic coinfection in coastal Kenyaen_US
dc.titleDevelopment of a specimen-sparing multichannel bead assay to detect antiparasite IgG4 for the diagnosis of Schistosoma and Wuchereria infections on the coast of Kenyaen_US
dc.typeArticleen_US


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