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Cytomegalovirus (CMV) Antibody, IgG

Code:18024

Synonyms
Антитела класса IgG к цитомегаловирусу (ЦМВ).Anti-CMV IgGCMV antibody, IgGCytomegalovirus (CMV) IgG antibodyIgG antibodies to cytomegalovirus
IncludesCytomegalovirus (CMV) IgG antibody

Analysis details

Methodology

  • Electrochemiluminescence immunoassay (ECLIA)

Expected Turnaround Time

1–2 days

Special Instructions

  • Avoid smoking for at least 30 minutes before the blood draw.

How to use

The Cytomegalovirus (CMV) Antibody, IgG test, also referred to as Anti-CMV IgG or CMV IgG antibody, is used to determine previous CMV infection and to assess immune status. In clinical scenarios suggestive of CMV, serologic status supports attribution of illness to CMV, particularly when Epstein–Barr virus testing is negative. In obstetric care, CMV IgG—used alone or with paired sera and/or IgG avidity—helps stratify the risk of congenital CMV. In immunocompromised hosts, CMV serology contributes to the diagnostic assessment of suspected CMV-related disease.

Limitations

Cytomegalovirus is a human herpesvirus that establishes lifelong latency and can reactivate. Transmission occurs through saliva, urine, semen, and blood, and by vertical routes in utero, during delivery, or via breast milk. Primary infection in immunocompetent persons is often asymptomatic or manifests as a mononucleosis-like syndrome. During pregnancy, primary maternal infection is associated with the risk of congenital CMV; a subset of congenitally infected infants develop symptomatic disease with findings such as microcephaly, intracranial calcifications, rash, hepatosplenomegaly, and sensorineural hearing loss. IgG antibodies develop within weeks after primary infection and persist for years. IgG avidity increases over time and helps differentiate recent primary infection (low avidity) from past infection or reactivation (high avidity). Because maternal IgG crosses the placenta, neonatal IgG serology does not establish congenital infection.

Reference interval
IndicationsPreconception or prenatal assessment of CMV serostatus and congenital CMV risk, or when fetal ultrasound findings raise concern for intrauterine infection, Evaluation of suspected CMV disease in immunocompromised individuals, Mononucleosis-like presentation with negative Epstein–Barr virus testing

Specimen Requirements

SpecimenRapid PCR specimen
ContainerRapid Test Cartridge / Swab

References

Adler S. P. Screening for cytomegalovirus during Pregnancy. Infect Dis Obstet Gynecol. 2011:1–9.

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

Lazzarotto T. et al. Why is cytomegalovirus the most frequent cause of congenital infection? Expert Rev Anti Infect Ther. 2011; 9(10): 841–843.

Belshe RB, ed. Textbook of Human Virology. Littleton, Mass: PSG Publishing Co;1984.

Drew WL. Controversies in viral diagnosis. Rev Infect Dis. 1986 Sep-Oct; 8(5):814-824. PubMed 3024292

Korones SB. Uncommon virus infections of the mother, fetus, and newborn: Influenza, mumps, and measles. Clin Perinatol. 1988 Jun; 15(2):259-272. PubMed 3288423

Lennette DA. Preparation of specimens for virological examination. In: Balows A, Hausler WJ, et al, eds. Manual of Clinical Microbiology. 5th ed. Washington, DC: ASM Press;1991:818-821.

Pfaller MA, Caliendo AM, Versalovic J. Detection of herpes simplex virus in CSF by PCR. In: Isenberg HD, ed. Clinical Microbiology Procedures Handbook. 2nd ed. Washington, DC: ASM Press: 2004:12.2.3.51-12.2.3.61.