Quantitative determination of cytomegalovirus IgG antibody by enzyme-linked immunosorbent assay (ELISA)
- 1 September 1979
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Microbiology
- Vol. 25 (9) , 1082-1086
- https://doi.org/10.1139/m79-165
Abstract
Quantitative determination of cytomegalovirus (CMV) human IgG antibody by ELISA performed in polystyrene trays was carried out and compared with results obtained by the routine complement fixation (CF) test. The antibody titres of all the sera determined by ELISA were higher than those detected by the CF test. Of the 27 sera negative (< 1:8) by the CF test, 22 of them were also negative (< 1:50) by ELISA. The other five CF negative sera were found to have low levels of antibody by ELISA. ELISA is a sensitive and specific assay for CMV antibody. The CMV antigen adsorbed readily to the microtitre plates and the test was simple to perform. The results of ELISA could be obtained in 5 to 6 h.A description of the test procedure is given including the method of CMV antigen attachment to the plates. The possibility of using paired sera at a single dilution in the ELISA test to detect seroconversion is discussed.This publication has 4 references indexed in Scilit:
- Enzyme-linked immunosorbent assay for detection of antibodies to influenza A and B and parainfluenza type 1 in sera of patientsJournal of Clinical Microbiology, 1978
- Enzyme-linked immunosorbent assay for diagnosis of rotavirus infections in calvesJournal of Clinical Microbiology, 1977
- Solid-phase enzyme immunoassay for immunoglobulin M antibodies to cytomegalovirusJournal of Clinical Microbiology, 1977
- ENZYME-IMMUNOASSAYS FOR ANTIBODIES IN MEASLES, CYTOMEGALOVIRUS INFECTIONS AND AFTER RUBELLA VACCINATION1976