Skip to main content
Bulletin of the World Health Organization logoLink to Bulletin of the World Health Organization
. 1984;62(3):463–466.

Use of an enzyme-linked immunosorbent assay to measure antigenaemia during acute plague*

James E Williams, Mary K Gentry, Carol A Braden, Flora Leister, Robert H Yolken
PMCID: PMC2536311  PMID: 6380787

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 antigen. ELISA-inhibition was used to confirm the specificity of the reactions.

This assay detected F1 antigen in two of ten sera from patients with acute bubonic plague and indicated that antigenaemia in man during plague may reach levels of 4-8 μg of F1 antigen per 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 antigenaemia did not have antibody, while two patients with antibody lacked antigenaemia.

Full text

PDF
463

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Soergel M. E., Schaffer F. L., Blank H. F. Solid-phase radioimmunoassay for detection of plague antigen in animal tissue. J Clin Microbiol. 1982 Nov;16(5):953–956. doi: 10.1128/jcm.16.5.953-956.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Williams J. E., Arntzen L., Robinson D. M., Cavanaugh D. C., Isaäcson M. Comparison of passive haemagglutination and enzyme-linked immunosorbent assay for serodiagnosis of plague. Bull World Health Organ. 1982;60(5):777–781. [PMC free article] [PubMed] [Google Scholar]
  3. Williams J. E., Robinson D. M. Requirement to confirm the specificity of ELISA reactions. Trans R Soc Trop Med Hyg. 1982;76(2):280–281. doi: 10.1016/0035-9203(82)90300-5. [DOI] [PubMed] [Google Scholar]
  4. Yolken R. H. Enzyme immunoassays for the detection of infectious antigens in body fluids: current limitations and future prospects. Rev Infect Dis. 1982 Jan-Feb;4(1):35–68. doi: 10.1093/clinids/4.1.35. [DOI] [PubMed] [Google Scholar]
  5. Yolken R. H., Leister F. J. Investigation of enzyme immunoassay time courses: development of rapid assay systems. J Clin Microbiol. 1981 Apr;13(4):738–741. doi: 10.1128/jcm.13.4.738-741.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Bulletin of the World Health Organization are provided here courtesy of World Health Organization

RESOURCES