H influenza b Antibody IgG
A common method for evaluating suspected antibody deficiency is to immunize the patient with an appropriately selected vaccine, such as Tetanus, and determine vaccine-specific antibody concentrations in a serum sample 3-4 weeks post-immunization compared to a pre-immunization sample.
ProcedureThe Haemophilus influenza type B capsular polysaccharide is used as a solid phase antigen in a sensitive microtiter EIA. The assay is calibrated against the standard from the Centre for biologics Evaluation and Research, US Food and Drug Administration: Lot 1983. The minimal protective level in non-vaccinated individuals is greater than or equal to 0.15 mcg/mL. The protective level expected in recently vaccinated individuals is greater than or equal to 1.0 mcg/mL. This test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
2-3 business days from receipt of specimen
| Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
|---|---|---|---|---|---|---|
| serum | 1121 | 86684 | Yes | 1 mL (min. 200 uL) |
0.11-90 mcg/mL |
|
0.11-90 mcg/mL
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for general informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
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