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Test Code EBVAB Epstein-Barr Virus Antibody Profile, Serum


Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Secondary ID

621373

Useful For

Diagnosis of Epstein-Barr virus (EBV) infectious mononucleosis or other EBV related infections

 

Identification of prior EBV infection as part of pre-immunosuppression screening

 

This assay is not intended for viral isolation or identification.

Profile Information

Test ID Reporting Name Available Separately Always Performed
MEBV EBV VCA IgM, S No Yes
GEBV EBV VCA IgG, S No Yes
NAEBV EBV NA IgG, S No Yes
INTEB Interpretation No Yes

Method Name

MEBV, GEBV, NAEBV: Enzyme-Linked Immunosorbent Assay (ELISA)

INTEB: Technical Interpretation

Specimen Type

Serum

Specimen Minimum Volume

0.4 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Frozen (preferred) 14 days
  Refrigerated  48 hours

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject
Heat-inactivated specimen Reject

Reference Values

Epstein-Barr Virus VIRAL CAPSID ANTIGEN (VCA) IgM ANTIBODY:

Negative

 

Epstein-Barr Virus VIRAL CAPSID ANTIGEN (VCA) IgG ANTIBODY:

Negative

 

EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN (EBNA) IgG ANTIBODY:

Negative

Interpretation

The profile has 3 components: viral capsid antigen (VCA) IgG, VCA IgM, and Epstein-Barr nuclear antigen (EBNA).

 

Presence of VCA IgM antibodies suggests an acute or recent primary infection with Epstein-Barr virus (EBV).

 

Presence of VCA IgG antibodies indicates infection sometime in the recent or remote past.

 

Antibodies to EBNA develop 6 to 8 weeks after primary infection and are detectable for life.

 

Refer to table below for interpretation of EBV antibody results.

VCA IgM result

VCA IgG result

EBNA IgG result

Interpretation

Negative

Positive

Negative

Results suggest recent EBV infection. The detection of only anti-VCA IgG should be interpreted with caution in immunocompromised patients, as this population may demonstrate diminishing or undetectable levels of anti-EBNA IgG antibodies.

Positive

Positive

Negative

Results suggest recent EBV infection.

Positive

Negative

Negative

Positive

Equivocal

Equivocal

Results suggest recent EBV infection.

Recommend follow-up testing in 10-14 days if clinically indicated.

Positive

Equivocal

Negative

Positive

Positive

Equivocal

Positive

Negative

Equivocal

Positive

Positive

Positive

Results may suggest recent EBV recovery or reactivation.

Positive

Equivocal

Positive

Positive

Negative

Positive

Negative

Negative

Negative

Results suggest no prior exposure to EBV. However, a second serum specimen should be tested in 10-14 days if clinically indicated.

Negative

Positive

Positive

Results suggest past EBV infection.

Negative

Negative

Positive

Negative

Equivocal

Positive

Negative

Positive

Equivocal

Detection of anti-VCA IgG only should be interpreted with caution in immunocompromised patients, as this population may demonstrate diminishing or undetectable levels of anti-EBNA IgG antibodies.

Recommend follow-up testing in 10-14 days if clinically indicated.

Equivocal

Negative

Positive

Results suggest past EBV infection.

Recommend follow-up testing in 10-14 days if clinically indicated.

Equivocal

Equivocal

Positive

 

 

 

Results with unclear clinical significance

Negative

Negative

Equivocal

Recommend follow-up testing in 10-14 days if clinically indicated.

Negative

Equivocal

Negative

Negative

Equivocal

Equivocal

Equivocal

Negative

Negative

Equivocal

Negative

Equivocal

Equivocal

Equivocal

Negative

Equivocal

Equivocal

Equivocal

Equivocal

Positive

Negative

Equivocal

Positive

Equivocal

Equivocal

Positive

Positive

Method Description

The ZEUS ELISA EBV (Epstein Barr virus) VCA (viral capture antigen) IgM, VCA IgG, and EBNA-1 (Epstein Barr nuclear antigen-1) IgG Test Systems are designed to detect IgM, IgG, IgG class antibodies to EBNA in human sera. Creation of the sensitized wells of the plastic microwell strips occurred using passive adsorption with EBV antigen. The test procedure involves three incubation steps. Test sera are diluted with the Sample Diluent provided. The IgM Sample Diluent contains antihuman IgG that precipitates and removes IgG and rheumatoid factor from the sample leaving IgM free to react with the immobilized antigen. During sample incubation any antigen specific antibody in the sample will bind to the immobilized antigen. The plate is washed to remove unbound antibody and other serum components. Peroxidase Conjugated goat ant-human IgM or IgG is added to the wells and the plate is incubated. The Conjugate will react with IgM or IgG antibody immobilized on the solid phase. The wells are washed to remove unbound Conjugate. The microwells containing immobilized peroxidase Conjugate are incubated with peroxidase Substrate Solution. Hydrolysis of the Substrate by peroxidase produces a color change. After a period of time the reaction is stopped and the color intensity of the solution is measured photometrically. The color intensity of the solution depends upon the antibody concentration in the original test sample.(Package inserts: EBV-VCA IgM Test System. Zeus Scientific, Inc.; 12/13/2017; EBV-VCA IgG Test System. Zeus Scientific, Inc.; 12/19/2017; EBNA-1 IgG Test System. Zeus Scientific, Inc.; 12/19/2017)

Day(s) Performed

Monday through Friday

Report Available

Same day/1 to 2 days

Specimen Retention Time

14 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

86664-EBNA

86665 x 2-VCA, IgG and IgM

LOINC Code Information

Test ID Test Order Name Order LOINC Value
EBVAB EBV Ab Profile, S 87554-2

 

Result ID Test Result Name Result LOINC Value
GEBV EBV VCA IgG, S 24114-1
INTEB Interpretation 69048-7
MEBV EBV VCA IgM, S 24115-8
NAEBV EBV NA IgG, S 5156-5