USE OF AN ENZYME-LINKED IMMUNOSORBENT-ASSAY TO MEASURE ANTIGENAEMIA DURING ACUTE PLAGUE
- 1 January 1984
- journal article
- research article
- Vol. 62 (3) , 463-466
Abstract
An enzyme-linked immunosorbent assay (ELISA) was developed to measure concentrations of the specific F1 antigen of the plague bacillus in biological fluids. The assay employed a monoclonal antibody to capture the antigen. Sensitivity of the assay was 0.4 ng of F1 antiben. ELISA-inhibition was used to confirm the specificity of the reactions. This assay detected F1 antigen in 2 of 10 sera from patients with acute bubonic plague and indicated that antigenemia in man during palque may reach levels of 4-8 .mu.g of F1 antigen/ml of serum. The probability for a correct serodiagnosis of plague was improved when the patients'' sera were tested for both antibody and antigen. Two patients with antigenemia did not have antibody, while 2 patients with antibody lacked antigenaemia.This publication has 6 references indexed in Scilit:
- Requirement to confirm the specificity of ELISA reactionsTransactions of the Royal Society of Tropical Medicine and Hygiene, 1982
- COMPARISON OF PASSIVE HEMAGGLUTINATION AND ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR SERODIAGNOSIS OF PLAGUE1982
- Enzyme Immunoassays for the Detection of Infectious Antigens in Body Fluids: Current Limitations and Future ProspectsClinical Infectious Diseases, 1982
- Investigation of enzyme immunoassay time courses: development of rapid assay systemsJournal of Clinical Microbiology, 1981