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IgA Subclasses
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Test Code
IGASUB
CPT Codes
82784, 82787 (x2)
Includes
IgA1, IgA2, and IgA, Serum
Preferred Specimen
2 mL serum
Patient Preparation
Fasting preferred
Minimum Volume
1 mL
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 5 days
Refrigerated: 15 days
Frozen: 30 days
Refrigerated: 15 days
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis • Lipemia
Methodology
Immunoturbidimetry
Setup Schedule
Set up: Sun, Thurs; Report available: 2-4 days
Reference Range
| IgA1 | |
| 6-11 months | 1-115 mg/dL |
| 1 year | 3-120 mg/dL |
| 2 years | 7-132 mg/dL |
| 3 years | 11-143 mg/dL |
| 4-7 years | 23-175 mg/dL |
| 8-11 years | 33-204 mg/dL |
| 12-17 years | 47-249 mg/dL |
| ≥18 years | 46-378 mg/dL |
| IgA2 | |
| 6-11 months | 0-19 mg/dL |
| 1 year | 0-23 mg/dL |
| 2 years | 1-23 mg/dL |
| 3 years | 1-25 mg/dL |
| 4-7 years | 2-33 mg/dL |
| 8-11 years | 2-37 mg/dL |
| 12-17 years | 4-50 mg/dL |
| ≥18 years | 13-91 mg/dL |
| IgA, Serum | |
| Cord Blood | 1-3 mg/dL |
| 1-28 days | 2-40 mg/dL |
| 1-3 months | 3-40 mg/dL |
| 4-6 months | 7-47 mg/dL |
| 7-11 months | 12-53 mg/dL |
| 1 year | 20-73 mg/dL |
| 2 years | 20-99 mg/dL |
| 3-5 years | 22-140 mg/dL |
| 6-8 years | 31-180 mg/dL |
| 9-11 years | 33-200 mg/dL |
| 12-16 years | 36-220 mg/dL |
| 17-60 years | 47-310 mg/dL |
| ≥61 years | 70-320 mg/dL |
Clinical Significance
IgA, the predominant immunoglobulin secreted at mucosal surfaces, consists of 2 subclasses. IgA1 is the major subclass and accounts for 80% of total IgA in serum, whereas IgA2 is the major subclass in secretions such as milk.
Low concentrations of IgA2 with normal IgA1 levels suggest an IgA2 deficiency.
Antigenic sites on the IgA subclasses are responsible for the anaphylactic transfusion reactions experienced by some patients totally deficient in either IgA1 or IgA2. After repeated transfusions, such patients may produce antibodies to these antigens. Thus, IgA subclasses are useful in evaluating patients with anaphylactic transfusion reactions.
Elevated concentrations of IgA2 with normal or low amounts of IgA1 suggest a clonal plasma cell proliferative disorder secreting a monoclonal IgA2. Grossly elevated levels of either subclass can occur in patients with IgA myeloma.
IgA subclasses are of further importance in certain pathogenic microorganisms, including Haemophilus influenzae, which are capable of enzymic cleavage of IgA1, leading to partial inactivation of this subclass. Recurrent sinopulmonary infections may, therefore, be related to deficiency of IgA2, which is resistant to these organisms.
Low concentrations of IgA2 with normal IgA1 levels suggest an IgA2 deficiency.
Antigenic sites on the IgA subclasses are responsible for the anaphylactic transfusion reactions experienced by some patients totally deficient in either IgA1 or IgA2. After repeated transfusions, such patients may produce antibodies to these antigens. Thus, IgA subclasses are useful in evaluating patients with anaphylactic transfusion reactions.
Elevated concentrations of IgA2 with normal or low amounts of IgA1 suggest a clonal plasma cell proliferative disorder secreting a monoclonal IgA2. Grossly elevated levels of either subclass can occur in patients with IgA myeloma.
IgA subclasses are of further importance in certain pathogenic microorganisms, including Haemophilus influenzae, which are capable of enzymic cleavage of IgA1, leading to partial inactivation of this subclass. Recurrent sinopulmonary infections may, therefore, be related to deficiency of IgA2, which is resistant to these organisms.
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Dr
Chantilly, VA 20153
Last Updated: November 30, 2021
