This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Google Scholar
Right arrow Articles by Bravo, D.
Right arrow Articles by Navarro, D.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bravo, D.
Right arrow Articles by Navarro, D.

 Previous Article  |  Next Article 

Clinical and Vaccine Immunology, June 2009, p. 885-888, Vol. 16, No. 6
1071-412X/09/$08.00+0     doi:10.1128/CVI.00123-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Evaluation of an Immunofiltration Assay That Detects Immunoglobulin M Antibodies against the ZEBRA Protein for the Diagnosis of Epstein-Barr Virus Infectious Mononucleosis in Immunocompetent Patients {triangledown}

Dayana Bravo, Beatriz Muñoz-Cobo, Elisa Costa, M. Angeles Clari, Nuria Tormo, and David Navarro*

Department of Microbiology, Hospital Clínico Universitario, Valencia, Spain

Received 21 March 2009/ Returned for modification 17 April 2009/ Accepted 21 April 2009

The performance of an immunofiltration assay (IMFA) that detects immunoglobulin M (IgM) antibodies to the Epstein-Barr virus (EBV) ZEBRA (BamHI Z EBV replication activator) protein was evaluated for the diagnosis of EBV infectious mononucleosis (IM) in immunocompetent patients. The test panel consisted of 47 sera displaying an EBV-specific antibody profile compatible with an acute primary EBV infection from patients with clinical and biological features of EBV IM, 20 sera from healthy individuals either with a past EBV infection or who were EBV seronegative, 20 sera displaying an equivocal EBV antibody pattern (viral capsid antigen IgG positive [VCA IgG+], VCA IgM+, and EBV nuclear antigen-1 IgG+), and 15 sera obtained from patients with a mononucleosis-like syndrome owing to cytomegalovirus, human herpesvirus 6, or parvovirus B19. Overall, the sensitivity and the specificity of the assay were found to be 92.5%, and 97.3%, respectively. The sensitivity of the assay for the diagnosis of heterophile antibody-negative EBV IM was 86.2%. The IMFA is rapid, easy to perform, and, thus, suitable for point-of-care testing, and it may be used as a first-line test for the diagnosis of acute EBV IM in immunocompetent patients.


* Corresponding author. Mailing address: Hospital Clínico Universitario, Av. Blasco Ibáñez 17, Valencia 46010, Spain. Phone: 34963864657. Fax: 34963864658. E-mail: David.Navarro{at}uv.es

{triangledown} Published ahead of print on 29 April 2009.


Clinical and Vaccine Immunology, June 2009, p. 885-888, Vol. 16, No. 6
1071-412X/09/$08.00+0     doi:10.1128/CVI.00123-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.