Herpes Simplex Virus Type 2 (HSV-2), Type-specific Antibodies, IgG

CPT: 86696
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Synonyms

  • HSV-2

Expected Turnaround Time

1 - 3 days


Related Documents


Specimen Requirements


Specimen

Serum


Volume

1.0 mL


Minimum Volume

0.5 mL (Note: This volume does not allow for repeat testing.)


Container

Red-top tube, gel-barrier tube or serum transfer tube


Storage Instructions

Refrigerate.


Stability Requirements

Temperature

Period

Room temperature

2 days

Refrigerated

7 days

Frozen

98 days

Freeze/thaw cycles

Stable x4


Causes for Rejection

Hemolysis; lipemia; grossly icteric; visible particulate matter; gross bacterial contamination


Test Details


Use

This test is used to detect IgG antibodies specific to HSV type 2 infection and confirm or rule out possible infection with herpes simplex type 2 virus in prenatal patients in whom HSV 2 infection can cause serious prenatal disease. In a patient with no history of lesion disease, a positive result for this test may be indicative that the primary infection was asymptomatic. The magnitude of the Index Value is not indicative of the amount of antibody present in the patient sample. Once infected by HSV, it is possible for a patient to shed virus without the development of lesions (asymptomatic shedding). This test does not indicate the site of HSV infection. There is a considerable homology between HSV-1 and HSV-2 antigens, so that antibodies formed against either virus are highly cross-reactive. This assay is based on glycoprotein G-2, purified from HSV-2 infected cells, and is specific for type 2 antibodies.


Limitations

Serum samples collected too early in the course of infection may not have detectable levels of HSV IgG. In cases of suspected early disease, a repeat serum specimen should be collected 14-21 days later and submitted for testing.

The predictive value of positive or negative results depends on the prevalence of disease and the pretest likelihood of HSV-1 and HSV-2.

False-positive results may occur. Repeat testing, or testing by a different method, may be indicated in some settings (e.g., patients with low likelihood of HSV infection).

This test is intended for qualitative determination only. The magnitude of the Index Value is not indicative of the amount of antibody present in the patient sample.


Methodology

Chemiluminescent immunoassay (CLIA)


References

American Academy of Pediatrics, American College of Obstetricians and Gynecologists. In: Kilpatrick SJ, Papile LA, eds. Guidelines for Perinatal Care, 8th Edition. ElkGrove, IL, and Washington, D.C.; 2017.
Landry LL. Immunoglobulin M for Acute Infection: True or False? Clin Vaccine Immuol. 2016 Jul 5;23(7):540-545.27193039
Miller JM, Binnicker MJ, Campbell S, et al. A Guide to Utilization of the Microbiology Laboratory for Diagnosis of Infectious Diseases: 2018 Update by the InfectiousDiseases Society of America and the American Society for Microbiology. Clin Infect Dis. 2018 Aug 31;67(6): e1-e94.29955859
US Preventive Services Task Force, Bibbins-Domingo K, Grossman DC, et al. Serologic Screening for Genital Herpes Infection: US Preventive Services Task ForceRecommendation Statement. JAMA. 2016 Dec 20;316(23):2525-2530.27997659
Workowski KA, Bachmann LH, Chan PH, et al. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187.34292926

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
164098 HSV-2 Ab, IgG 5209-2 164097 HSV 2 IgG, Type Spec index 5209-2

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