Herpes Simplex Virus (HSV) Types 1/2 Antibodies, IgM, Immunoblot
Code:17008
| Includes | HSV-1 IgM antibodies HSV-2 IgM antibodies |
|---|
Analysis details
Methodology
- Western blot
Expected Turnaround Time
1 day
Special Instructions
- Do not eat for 2–3 hours before the blood draw; water is allowed.
- Avoid smoking for at least 30 minutes prior to specimen collection.
How to use
Herpes Simplex Virus (HSV) Types 1/2 Antibodies, IgM, Immunoblot is used to evaluate HSV 1/2–associated disease and to corroborate equivocal or weak-positive HSV IgM or IgG enzyme immunoassay findings. The test aids diagnostic assessment in clinical settings where early infection is suspected, including HSV encephalitis, intrauterine fetal infection, and disseminated herpesvirus infection. Synonyms such as HSV 1/2 and herpes simplex virus types 1 and 2 are commonly used for this evaluation.
Limitations
HSV-1 and HSV-2 are enveloped DNA viruses that establish lifelong latency in sensory ganglia with intermittent reactivation. Transmission occurs through respiratory droplets, direct contact, sexual exposure, and across the placenta. Clinical manifestations span gingivostomatitis, genital herpes, keratoconjunctivitis (more often associated with HSV-1), encephalitis, intrauterine infection, fetal loss, and disseminated neonatal disease (commonly linked to HSV-2). Primary maternal infection in the second or third trimester increases the likelihood of fetal infection. HSV is not considered a teratogen, and clinical outcomes differ from other TORCH pathogens. Immunoblot methodology detects antibodies to discrete HSV antigens with strong analytical performance, provides confirmation of screening enzyme immunoassay results, supports type-specific interpretation based on antigen reactivity patterns (for example, gG-based responses), and assists with infection staging and the recognition of subclinical HSV-1 and HSV-2.
| Unit | qualitative | ||||
|---|---|---|---|---|---|
| Reference interval |
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| Indications | Evaluation of suspected HSV meningoencephalitis., First episode of genital herpes occurring in the second or third trimester of pregnancy., Recurrent genital herpes during the second or third trimester of pregnancy., Workup for possible intrauterine HSV infection with features such as fetal growth restriction, hepatosplenomegaly, or hydrocephalus., Concern for disseminated HSV in immunocompromised individuals, pregnant patients, or neonates., Confirmation of equivocal or weakly positive HSV IgM or IgG enzyme immunoassay results., Inclusion in the differential diagnosis of urogenital infections., Preconception assessment when a partner may have been exposed to HSV., Assessment for intrauterine infection in the setting of placental insufficiency., Testing in the context of HIV infection or other immunodeficiency states. |
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Storage Instructions | Refrigerated, Frozen |
References
Biasi RL, Kleinschmidt-DeMasters BK, Weinberg A, Tyler KL. Use of PCR for the diagnosis of herpesvirus infections of the central nervous system. J Clin Virol. 2002 Jul;25 Suppl 1:S5-11.
Espy MJ, Uhl JR, Mitchell PS, Thorvilson JN, Svien KA, Wold AD, Smith TF. Diagnosis of herpes simplex virus infections in the clinical laboratory by LightCycler PCR. J Clin Microbiol. 2000 Feb;38(2):795-9.
Avgil M, Ornoy A. Herpes simplex virus and Epstein-Barr virus infections in pregnancy: consequences of neonatal or intrauterine infection. Reprod Toxicol. 2006 May;21(4):436-45.