EBV Serology Panels Available in Core Laboratory
Effective Tuesday, December 11, 2012, the University of Iowa Hospitals and Clinics core clinical chemistry laboratory will begin offering two panels of serologic testing for Epstein-Barr Virus (EBV) on the BioRad Bioplex 2200 analyzer. The turnaround time is 3 hrs or less from receipt in laboratory. These tests will include an interpretative result and table derived from large retrospective study of EBV serology panel results (Klutts JS et al., J Clin Microbiol 47: 3204-3410, 2009).
Details on the tests are as follows:
(1) Epstein-Barr Virus Acute Panel (LAB7810)
The acute panel contains tests for heterophile IgM (equivalent to Monospot) and viral capsid antibody (VCA) IgM and is intended for workup of possible acute EBV infection. Heterophile IgM is relatively less sensitive than VCA IgM in acute EBV infection. Negative results for both VCA IgM and heterophile antibody rule out acute EBV infection with high sensitivity.
The EBV acute panel yields 4 possible patterns of results that have the following likely interpretations (equivocal results being treated as negative in the table):
Heterophile IgM | VCA IgM | Likely Interpretation |
Neg | Neg | No acute EBV infection |
Neg | Pos | Acute EBV infection |
Pos | Pos | Acute EBV infection |
Pos | Neg | Unusual pattern, difficult to interpret |
The core laboratory will continue to offer Monospot (LAB327) which provides the most rapid turnaround for acute EBV infection.
(2) Epstein-Barr Virus, Full AB Panel (LAB4584)
The EBV full panel contains tests for heterophile IgM antibody, VCA IgM, VCA IgG, and EBV nuclear antigen (EBNA) IgG. The full EBV panel is intended to clarify or confirm equivocal or negative Monospot tests (especially in patients at risk for splenic rupture) or for assessment of EBV infection in immunocompromised patients (including transplant recipients).
The EBV panel yields 16 possible patterns of results that have the following likely interpretations (equivocal results being treated as negative in the table):
Heterophile IgM | VCA IgM | VCA IgG | EBNA IgG | Likely Interpretation |
Neg | Neg | Neg | Neg | EBV naïve |
Neg | Pos | Neg | Neg | Primary acute EBV infection |
Pos | Neg | Neg | Neg | Primary acute EBV infection |
Pos | Pos | Neg | Neg | Primary acute EBV infection |
Neg | Pos | Pos | Neg | Primary acute EBV infection |
Pos | Neg | Pos | Neg | Primary acute EBV infection |
Pos | Pos | Pos | Neg | Primary acute EBV infection |
Neg | Pos | Neg | Pos | Recov/react EBV infection1 |
Neg | Pos | Pos | Pos | Recov/react EBV infection1 |
Pos | Neg | Pos | Pos | Recov/react EBV infection1 |
Pos | Pos | Neg | Pos | Recov/react EBV infection1 |
Pos | Pos | Pos | Pos | Recov/react EBV infection1 |
Neg | Neg | Pos | Neg | Past EBV infection (not active) |
Neg | Neg | Pos | Pos | Past EBV infection (not active) |
Pos | Neg | Neg | Pos | Unknown significance2 |
Neg | Neg | Neg | Pos | Unknown significance1 |
1 Recovery from EBV infection or reactivated EBV infection
2 Uncommon patterns of unknown clinical significance
Questions should be directed to Matthew Krasowski, MD, PhD, medical director of the Clinical Chemistry Laboratory (384-9380, matthew-krasowski@uiowa.edu).