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
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.