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Biomarkers · Chemical

Rubella Antibodies, IgM

Understand what Rubella Antibodies, IgM signals

Primary unit
AU/mL
LOINC codes
5334-8, 5335-5, 20464-4, 40678-5, 5126-8, 5206-8, 5209-2, 5388-4
Commercial laboratory assays
4

We have not added a physiological summary for this biomarker yet. Compare the commercial laboratory assays and population reference ranges below.

Compare commercial laboratory assays for Rubella Antibodies, IgM

Check orderable catalog codes, specimen types, fasting requirements, and demographic reference ranges across laboratories.

Rubella Antibodies (IgG, IgM) Diagnostic

Laboratory
Quest Diagnostics
Test code
37673
Specimen
Serum
Fasting
Not stated
LOINC
5334-8, 5335-5

Laboratory assay overview

Rubella (German Measles) is a common and usually benign viral infection of children. IgM antibody is detectable 11-25 days after the onset of exanthem, in most individuals 15-25 days after vaccination, and in 90-97% of infants with congenital rubella between 2 weeks and 3 months after birth. Acute and convalescent IgG titers may be interpreted to identify a >30% rise in the antibody index. A positive IgG antibody indicates successful immunization or past exposure.

View complete laboratory reference notes

See Laboratory Report

Quest Diagnostics test directory, test code 37673

Rubella Antibodies, IgM

Laboratory
Labcorp
Test code
096537
Specimen
Serum
Fasting
Not stated
LOINC
5335-5
Turnaround
1 - 3 days

Laboratory assay overview

For the in vitro detection of IgM antibodies specific for rubella. IgM antibodies are associated with acute viral infections. IgM detection is useful in the following situations: evidence of infection can be obtained from only one acute phase specimen if the IgM results are positive; the IgM test can also be used to differentiate between primary infection and re-exposure. Rubella-specific IgM is found in virtually all infected patients by three weeks postdevelopment of a rash. Rubella-specific IgM is also found in 80% of postvaccination patients by three weeks. Congenitally infected infants will show an IgM response at 2 to 12 weeks postnatally.

View complete laboratory reference notes

• Negative: <20.0 AU/mL • Equivocal: 20.0−24.9 AU/mL • Positive: >24.9 AU/mL

Labcorp test directory, test code 096537

Rubella Antibody (IgM)

Laboratory
Quest Diagnostics
Test code
4422
Specimen
Serum
Fasting
Not stated
LOINC
5335-5

Laboratory assay overview

Rubella is an acute exanthematous viral infection of children and adults. Rash, fever and lymphadenopathy characterize the illness. While many infections are subclinical, this virus has the potential to cause fetal infection with resultant birth defects. In the absence of a current or recent infection, a demonstration of specific IgG on a serum sample is evidence of immunity to rubella. A positive rubella IgM result does not necessarily indicate current or recent infection. Without a history of exposure to rubella or symptoms consistent with rubella, the IgM result may be difficult to interpret. Rubella IgM can be false positive due to other causes (e.g., parvovirus, rheumatoid factor, cytomegalovirus). Rubella IgM may also persist for more than 12 months after vaccination or natural infection. For a serologic diagnosis of congenital rubella in the neonatal period, antibody to rubella virus should be measured in both infant and maternal sera. If IgM is detected in a newborn infants serum, it is probable that transplacental rubella infection has occurred.

Quest Diagnostics population reference ranges

Quest Diagnostics calculates these statistical intervals for this specific assay and demographic group, not as universal optimal targets.

PopulationRange
AU/mLInterpretation
<20.00Negative
20.00-24.99Equivocal
≥25.00Positive
View complete laboratory reference notes

AU/mL Interpretation <20.00 Negative 20.00-24.99 Equivocal ≥25.00 Positive

Quest Diagnostics test directory, test code 4422

Torch Panel, Acute

Laboratory
Quest Diagnostics
Test code
12596
Specimen
Serum
Fasting
Not stated
LOINC
20464-4, 40678-5, 5126-8, 5206-8, 5209-2, 5335-5, 5388-4
View complete laboratory reference notes

See individual tests

Quest Diagnostics test directory, test code 12596

Verify these ranges and sources

We compile every detail above directly from named laboratory directories and published clinical studies. Laboratories calculate standard reference intervals from the statistical distribution of tested populations for a specific assay method and demographic group, rather than setting universal optimal targets.

Always review your personal lab results with a licensed clinician, or track your lab history and health goals in Aumnivida.

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