Return

Антитела к вирусу Варицелла-Зостер (VZV, IgM)

Code:17031

Synonyms
Антитела класса IgM к VZVиммуноглобулины класса M к вирусу опоясывающего лишая и ветряной оспы.Anti-varicella zoster virus IgMImmunoglobulin M antibodies to varicella-zoster virusVaricella zoster virus (VZV) IgM antibodiesVaricella-zoster virus antibodies, IgMVZV IgM

Analysis details

Methodology

Expected Turnaround Time

1–2 days

Special Instructions

  • Do not smoke for at least 30 minutes before the blood draw.

How to use

Varicella Zoster Virus (VZV) IgM, also referred to as anti‑VZV IgM, assists in determining the cause of acute vesicular eruptions consistent with varicella (chickenpox) or herpes zoster (shingles), especially when the presentation is atypical or when other viral exanthems are in the differential. Because IgM appears early and declines rapidly, the test is used to document recent primary infection or reactivation and to aid evaluation of congenital varicella; detection of VZV‑specific IgM in a newborn supports congenital varicella syndrome. Assessment of immune status is performed with VZV IgG, not IgM.

Limitations

Varicella zoster virus (VZV) causes two clinical syndromes: primary varicella (chickenpox) and reactivation disease (herpes zoster or shingles). Although both conditions are often diagnosed clinically, laboratory testing is valuable in atypical cases. Transmission occurs by the airborne route with an incubation period of approximately 10–21 days. Varicella typically begins with fever and malaise followed by a diffuse vesicular rash; lesions crust and resolve over about two weeks, usually without scarring. Primary infection generally confers lifelong immunity. Varicella in pregnancy may be severe for the mother and is associated with varicella pneumonia in about 20% of cases. Fetal risks include congenital varicella syndrome characterized by cutaneous scarring, limb hypoplasia, microcephaly, encephalitis, and ocular involvement. Maternal infection near delivery can result in severe neonatal varicella with risk of death. Evaluation of immunity in this setting relies on VZV IgG rather than IgM, as IgM reflects only recent infection. After primary infection, VZV establishes latency in sensory neurons and can reactivate with stress, immune suppression, or exposure to cold, producing herpes zoster. Prodromal malaise and fever are followed by pain, paresthesia, or pruritus over an affected dermatome; a unilateral vesicular eruption typically appears 1–3 days later. Neuralgia may persist for about a month after the rash resolves. Immunoglobulin M (IgM) antibodies appear first, then decline as IgG increases; IgM can be undetectable if testing is delayed. During zoster, IgM may rise transiently. Accordingly, VZV IgM testing is most informative for confirming recent infection or reactivation.

Reference interval
IndicationsGeneralized pruritic vesicular exanthem with lesions in different stages of evolution with fever, headache, and malaise, consistent with varicella (chickenpox), Unilateral dermatomal vesicular eruption accompanied by localized neuropathic pain and systemic symptoms, consistent with herpes zoster (shingles), Herpes zoster involving the face, ocular, or auricular dermatomes, or other nontruncal sites, Suspected zoster sine herpete (herpes zoster without rash), including neurologic complications such as facial nerve palsy, vertigo, hearing loss, or cerebellar ataxia

Possible Causes of Abnormal Results

Increased levels

  • cross-reactivity with herpes simplex virus infection

Specimen Requirements

SpecimenSerum
ContainerRed-top tube, no additive (serum)

References

Dobec M. et al. Serology and serum DNA detection in shingles. Swiss Med Wkly. 2008; 138:47 – 51.

Gardella C. et al. Managing varicella zoster infection in pregnancy. Cleve Clin J Med. 2007; 74(4):290-296.

Goldman's Cecil Medicine. 24th ed. Goldman L, Schafer A.I., eds. Saunders Elsevier; 2011.

Pupco A. et al. Herpes zoster during pregnancy. Can Fam Physician. 2011; 57(10):1133.