Rubella Antibodies, IgG
Code:17003|CPT:86762|LOINC:5334-8
| Includes | Rubella Antibodies, IgG |
|---|
Analysis details
Methodology
- Chemiluminescent immunoassay (CLIA)
- Immunoblot
Expected Turnaround Time
1 day
Special Instructions
- Avoid food for 2–3 hours before the blood draw; plain water is allowed.
- Do not smoke during the 30 minutes preceding specimen collection.
How to use
Rubella Antibodies, IgG (anti‑rubella IgG; German measles antibodies) is used to establish immunity following prior infection or immunization, including routine preconception and antenatal assessments. It also identifies individuals without immunity who may benefit from vaccination. In addition, the test helps clarify equivocal or discordant serologic results and supports evaluation of neonates for possible congenital rubella when maternal infection during pregnancy is suspected or confirmed.
Limitations
Following acute rubella, IgM appears first, whereas rubella‑specific IgG develops later and generally remains detectable for life, indicating prior infection or vaccine‑induced immunity. Rubella is a typically mild, self‑limited rash illness transmitted via respiratory droplets. However, primary infection in the first trimester is associated with a high risk of miscarriage, stillbirth, or congenital rubella syndrome featuring multisystem involvement, including sensorineural hearing loss, cataracts, cardiac anomalies, microcephaly, and hepatic disease. IgG seropositivity supports immune protection due to prior exposure or vaccination. Immunoblot techniques can demonstrate antibodies directed against individual rubella viral antigens, which may help characterize the pattern of the immune response.
| Unit | index | ||||
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| Reference interval |
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| Indications | Clinical signs and symptoms compatible with rubella infection, Clarification of borderline or conflicting serologic results by enzyme immunoassay (EIA), Preconception or prenatal screening to document rubella immunity, Assessment of possible maternal rubella during pregnancy, including suspected rubella embryopathy, Workup of a potentially false‑positive rubella IgM due to cross‑reactivity (eg, Epstein–Barr virus, cytomegalovirus, parvovirus B19) or rheumatoid factor, Determination of immune status to guide vaccination or revaccination planning, Evaluation of newborns for congenital rubella syndrome when maternal infection is suspected or confirmed, Contribution to the differential diagnosis of a generalized exanthem (eg, measles, scarlet fever, allergic exanthema, enteroviral infection) |
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Volume | 0.5 mL (min 0.2 mL) |
| Storage Instructions | Room temperature, Refrigerated, Frozen |