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Cytomegalovirus (CMV) Antibody, IgG

Code:18028

Synonyms
Антитела класса IgG к цитомегаловирусу (ЦМВ).Anti-CMV IgGCMV Antibody, IgGCMV IgG antibodiesCytomegalovirus (CMV) IgG antibodiesCytomegalovirus IgG
IncludesCytomegalovirus (CMV) IgG antibody

Analysis details

Methodology

  • Electrochemiluminescence immunoassay (ECLIA)

Expected Turnaround Time

1–2 days

Special Instructions

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

How to use

The Cytomegalovirus (CMV) Antibody, IgG test—also known as CMV IgG or Anti-CMV IgG—establishes CMV serostatus and evidence of past infection. In patients with compatible symptoms, results are interpreted with clinical findings and adjunctive studies such as CMV IgM or nucleic acid testing to assess suspected CMV infection. In preconception and prenatal care, CMV IgG assists in estimating the risk of congenital CMV and, when paired with IgG avidity testing or documented seroconversion, helps differentiate recent primary maternal infection from prior infection or reactivation. In immunocompromised populations, including transplant candidates/recipients and persons with advanced HIV, it supports baseline serostatus determination and risk stratification.

Limitations

Cytomegalovirus is a human herpesvirus that establishes lifelong latency with the capacity for reactivation. Transmission occurs through body fluids and through vertical routes during pregnancy, delivery, or breastfeeding. In immunocompetent hosts, primary infection is frequently asymptomatic or presents as a mononucleosis-like syndrome, whereas severe disease is seen in immunocompromised individuals. Congenital CMV most often follows primary maternal infection and carries a risk of fetal infection. Among congenitally infected infants, a subset develops manifestations that include microcephaly, intracranial calcifications, hepatosplenomegaly, and sensorineural hearing loss. Following primary infection, CMV IgG levels rise within weeks and then persist. IgG avidity increases over months; low avidity supports recent primary infection, whereas high avidity is consistent with remote infection or reactivation. Serologic findings should be integrated with the clinical context and, when indicated, CMV IgM, nucleic acid testing, or other supporting assays.

Reference interval
IndicationsPreconception or prenatal evaluation to determine CMV IgG serostatus and estimate congenital CMV risk, including assessment when fetal ultrasound findings raise concern for congenital infection, Assessment of suspected CMV disease in immunocompromised individuals, Mononucleosis-like illness in which Epstein–Barr virus testing is negative

Specimen Requirements

SpecimenUnspecified specimen
ContainerPer Test Requirement
Storage InstructionsRefrigerated, Frozen

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.

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

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.