Detection of the schistosome circulating cathodic antigen by enzyme immunoassay using biotinylated monoclonal antibodies

We have developed an enzyme immunoassay (EL-ISA) for the quantification of the schistosome circulating cathodic antigen (CCA), a glycoprotein associated with the syncitium lining the gut of the parasite. A mouse monoclonal antibody of IgG 3 isotype was used as coating (antigen-capture) antibody, whi...

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Veröffentlicht in:Transactions of the Royal Society of Tropical Medicine and Hygiene 1990-11, Vol.84 (6), p.815-818
Hauptverfasser: De Jonge, N., Kremsner, P.G., Krijger, F.W., Schommer, G., Ffflié, Y.E., Kornelis, D., van Zeyl, R.J.M., Van Dam, G.J., Feldmeier, H., Deelder, A.M.
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Sprache:eng
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Zusammenfassung:We have developed an enzyme immunoassay (EL-ISA) for the quantification of the schistosome circulating cathodic antigen (CCA), a glycoprotein associated with the syncitium lining the gut of the parasite. A mouse monoclonal antibody of IgG 3 isotype was used as coating (antigen-capture) antibody, while a biotinylated mouse monoclonal IgM was used as second (antigen-detecting) antibody. Streptavidin-alkaline phosphatase was used as enzyme label. The lower detection limit of the assay was 1·0 ng of the trichloroacetic acid soluble fraction of adult worm antigen (AWA-TCA) per ml, which corresponds to approximately 0·2 ng CCA per ml. The ELISA showed a linear range from 1·0 to 62·5 ng AWA-TCA per ml. Serum and urine samples of 16 individuals infected with Schistosoma mansoni (egg counts ranging from 5 to 4820 eggs per gram of faeces) were tested in the assay. Antigen titres ranged from
ISSN:0035-9203
1878-3503
DOI:10.1016/0035-9203(90)90094-U