SEROLOGICAL DIAGNOSIS OF INFECTIOUS-MONONUCLEOSIS USING 3 ANTI-EPSTEIN-BARR VIRUS RECOMBINANT ELISAS

Citation
I. Farber et al., SEROLOGICAL DIAGNOSIS OF INFECTIOUS-MONONUCLEOSIS USING 3 ANTI-EPSTEIN-BARR VIRUS RECOMBINANT ELISAS, Journal of virological methods, 42(2-3), 1993, pp. 301-308
Citations number
13
Categorie Soggetti
Virology,"Biochemical Research Methods
ISSN journal
01660934
Volume
42
Issue
2-3
Year of publication
1993
Pages
301 - 308
Database
ISI
SICI code
0166-0934(1993)42:2-3<301:SDOIU3>2.0.ZU;2-P
Abstract
A new Epstein-Barr virus (EBV) ELISA system (Biotest Anti-EBV recombin ant) was evaluated for usefulness for routine diagnosis of EBV primary infection. The assay system is composed of three different microtest plates coated with three highly purified recombinant EBV antigens. The early antigens p138 (BALF2, truncated) and p54 (BMRF1, whole sequence ) are used as a mixture for testing IgM (assay 1) and IgG (assay 2) an tibodies. In addition, the EBNA-1 antigen p72 (BKRF1, carboxy-half) is used for detecting IgG antibodies (assay 3). Three panels of sera wer e examined in direct comparison with standard immunofluorescence (IF): Specimens of (i) 120 infectious mononucleosis (IM) patients, (ii) 60 patients with acute CMV infection, toxoplasmosis or rheumatic disease, respectively, and (iii) 185 healthy blood donors as a control group. 119 IM patients were clearly recognized as having acute primary infect ion (sensitivity 99.2% compared to VCA-IgM by IF). Three apparently fa lse-positive results were obtained with patients of other diseases and none within the control group (specificity 98.8%). The data suggest t hat the recombinant ELISA can be used advantageously for standardized rapid diagnosis of acute EBV primary infection.