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Epic Test Code LAB2457 Epstein-Barr Virus Antibody Profile, Serum

Additional Codes

MML: EBVAB


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.


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

Reporting Name

EBV Ab Profile, S

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

Clinical Information

Epstein-Barr virus (EBV), a member of the herpesvirus group, is the etiologic agent of infectious mononucleosis. Infection with EBV usually occurs early in life. For several weeks to months after acute onset of the infection, EBV is spread by upper respiratory secretions that contain the virus. Among the EBV-associated clinical manifestations, infectious mononucleosis is the most common. EBV infection can be severe in immunosuppressed patients who may develop lymphoproliferative syndromes, especially in patients with advanced HIV and in patients who have undergone kidney or bone marrow transplantation. Other, rare manifestations include African-type Burkitt lymphoma and nasopharyngeal carcinoma.

 

EBV does not grow in standard cell cultures and molecular testing is the primary means of diagnosis and monitoring response to therapy in immunosuppressed patients. Serologic testing for EBV remains important for diagnosis of infectious mononucleosis in otherwise healthy individuals and for pre-transplant or pre-immunosuppression screening purposes.

 

The majority of infections in healthy individuals can be identified by testing patient sera for heterophile antibodies using a rapid latex slide agglutination test (MONOS / Infectious Mononucleosis, Rapid Test, Serum). Heterophile antibodies usually appear within the first 3 weeks of illness but decline rapidly within thereafter. However, heterophile antibodies fail to develop in about 10% of adults and in more than 75% of infants and young children under the age of 4. In cases where EBV is suspected but the heterophile antibody is not detected or if confirmation is needed, or if patients are undergoing pre-immunosuppression screening, evaluation of EBV-specific antibodies, including assessment for IgM and IgG against the EBV viral capsid antigen and IgG against the EBV nuclear antigen is useful.

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

Cautions

Specimens collected too early during the course of the disease may not contain detectable antibodies to Epstein-Barr virus (EBV). Another specimen collected 1 to 2 weeks later may be required.

 

Test results should be evaluated in relation to patient symptoms, clinical history, and other laboratory findings.

 

The timing of the appearance of IgG antibodies to viral capsid antigen (VCA) or Epstein-Barr nuclear antigen or IgM antibodies to VCA is subject to variations among individuals and serological assays.

 

This assay's performance characteristics with immunosuppressed individuals, newborns, cord blood, or matrices other than human serum have not been established.

 

Assay performance characteristics have not been established for the diagnosis of nasopharyngeal carcinoma, Burkitt lymphoma, and other EBV-associated lymphomas.

 

Anti-VCA-specific IgG may compete with IgM for binding sites, leading to false-negative results. Rheumatoid factor (RF), in the presence of specific IgG, may contribute to false-positive results. The absorbent in the VCA IgM diluent is intended to neutralize the effects of RF and specific IgG. Studies have shown that the absorbent was able to neutralize up to 98% of the activity in a specimen known to contain 3328 IU/mL of RF activity.

 

Testing for VCA IgM should not be performed as a screening procedure on the general population. The predictive value of positive or negative results depends on the pretest likelihood of Epstein-Barr-associated disease being present. Testing should only be performed when clinical evidence suggests the diagnosis of this syndrome.

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

NY State Approved

Yes