Test Code HRSPF Horse Dander, IgE with Reflex to Horse Dander Component, IgE, Serum
Ordering Guidance
For a listing of allergens available for testing, see Allergens - Immunoglobulin E (IgE) Antibodies
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.6 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
Evaluating patients with suspected horse dander allergy
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
HRSPR | Horse Dander Component, IgE, S | No | No |
Testing Algorithm
Testing begins with analysis of total horse dander IgE. If horse dander total IgE is negative (<0.10 kU/L), testing is complete.
If horse dander total IgE is 0.10 kU/L or more, then horse dander component (Equ c 1) testing is performed at an additional charge.
Special Instructions
Method Name
Fluorescent Enzyme Immunoassay (FEIA)
Reporting Name
Horse Dander Component Reflex, SSpecimen Type
SerumSpecimen Minimum Volume
0.4 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 90 days |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Clinical Information
Horse (equine) allergen sensitization occurs in approximately 5 to 15% of individuals exposed to horses in occupational settings. The assessment of allergy to horses is dependent upon the presence of compatible clinical symptoms in the context of exposure, with support from identification of potential equine-specific IgE allergen antibodies, either by skin testing or in vitro serology testing. In vitro testing has generally focused on assessing for the presence of IgE antibodies to total horse allergen extracts.
There is a correlation between total horse IgE allergen antibodies and an increased likelihood of a clinical allergic response. Once an elevated antibody response to total horse dander IgE extract is established, assessment for the presence of specific IgE antibodies to the major equine component will be performed. This may yield additional, potentially useful information for the clinical assessment of allergy and sensitization. During horse component allergen IgE antibody testing, the presence of IgE antibodies specific for the potential allergenic individual protein, namely Equ c 1, is assessed. The determination of the relative amount of IgE antibody to specific component can aid in assessment of the potential strength and type of allergenic response.
While several horse allergens have been described, the lipocalin Equ c 1 is the major horse allergen, and antibodies to this allergen are present in 76% of individuals exhibiting allergy to horses. The main source of exposure of Equ c 1 is inhalation. However, individuals can be exposed by contact with contaminated clothing and, potentially, through horse bites. Mattresses containing horsehair may also be a potential route of exposure. Individuals who are allergic to horses may exhibit allergic rhinitis, conjunctivitis, asthma, anaphylaxis, and allergy to other foods and animals.(1) To date, the existence of completely hypoallergenic horse breeds has not been verified.
Sensitization to horses may also occur through cross-reactivity, with as many as 30% of individuals with pet allergy also reporting allergic reaction to horses. As many as 50% of individuals with cross-reactive allergen sensitization are caused by cross reactive to horse lipocalin as represented by Equ c 1. Cross-reactivity has been shown to exist between horse lipocalin allergen Equ c 1, cat lipocalin allergen Fel d4, and dog lipocalin allergen Can f 6.
Reference Values
Class |
IgE kU/L |
Interpretation |
0 |
<0.10 |
Negative |
0/1 |
0.10-0.34 |
Borderline/equivocal |
1 |
0.35-0.69 |
Equivocal |
2 |
0.70-3.49 |
Positive |
3 |
3.50-17.4 |
Positive |
4 |
17.5-49.9 |
Strongly positive |
5 |
50.0-99.9 |
Strongly positive |
6 |
≥100 |
Strongly positive |
Concentrations of 0.70 kU/L or more (class 2 and above) will flag as abnormally high.
Reference values apply to all ages.
Interpretation
When detectable total horse dander IgE antibody is present (≥0.10 IgE kUa/L), additional specific component IgE antibody testing will be performed. If the specific allergenic horse dander component IgE is detectable (≥0.10 IgE kUa/L), an interpretative report will be provided.
When the sample is negative for total horse dander IgE antibody (<0.10 IgE kUa/L), additional testing for specific horse dander component IgE antibodies will not be performed. Negative IgE results for total horse dander antibody may indicate a lack of sensitization to potential horse dander allergenic components.
Cautions
Clinical correlation of results from in vitro IgE testing with a patient history of allergic or anaphylactic responses to horse dander is recommended.
-Negative results for IgE to total horse dander and any horse dander components do not completely exclude the possibility of clinically relevant allergic responses upon exposure to horse dander.
-Positive results for IgE to total horse dander or any potential horse dander allergenic components are not diagnostic for horse dander allergy and only indicate that the patient may be sensitized to horse dander or a cross-reactive allergen.
Testing for IgE antibodies may not be useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists or in patients whose medical management does not depend upon identification of allergen specificity.
False-positive results for IgE antibodies may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding to allergen solid phases.
Method Description
Specific IgE from the patient's serum reacts with the allergen of interest, covalently coupled to an ImmunoCAP. After washing away nonspecific IgE, enzyme-labeled anti-IgE antibody is added to form a complex. After incubation, unbound anti-IgE is washed away, and the bound complex incubated with a developing agent. After stopping the reaction, the fluorescence of the eluate is measured. Fluorescence is proportional to the amount of specific IgE present in the patient's sample (ie, the higher the fluorescence value, the more IgE antibody is present).(Package insert: ImmunoCAP System Specific IgE FEIA. Phadia AB; Rev 06/2020)
Day(s) Performed
Monday through Friday
Report Available
Same day/1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86003
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
HRSPF | Horse Dander Component Reflex, S | 6143-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
HORS1 | Horse Dander, IgE, S | 6143-2 |