Test Catalog

Test Id : DOGPF

Dog Dander, IgE, with Reflex to Dog Dander Components, IgE, Serum

Useful For
Suggests clinical disorders or settings where the test may be helpful

Evaluating patients with suspected dog dander allergy

Highlights

The determination of the relative amount of IgE antibody to total dog dander and IgE antibodies to specific dog dander components, may aid in assessment of the potential strength and type of allergenic response to dog dander.

 

IgE antibody to total dog dander extract will initially be tested.

 

If detectable total specific dog dander IgE antibody is present, additional component dog dander allergen antibody testing will be performed. This is comprised of testing for IgE antibodies to the potential allergens Can f 1, Can f 2, Can f 3, Can f 4, Can f 5, and Can f 6.

Reflex Tests
Lists tests that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial tests.

Test Id Reporting Name Available Separately Always Performed
DOGPR Dog Dander Components, IgE, S No No

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Testing begins with analysis of dog dander IgE. If dog dander IgE is negative (<0.10 kU/L), testing is complete.

 

If dog dander IgE is 0.10 kU/L or more, then 6 dog dander components (Can f 1, Can f 2, Can f 3, Can f 4, Can f 5, Can f 6) are performed at an additional charge.

Method Name
A short description of the method used to perform the test

Fluorescent Enzyme Immunoassay (FEIA)

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Dog Dander Component Reflex, S

Aliases
Lists additional common names for a test, as an aid in searching

Can f1

Can f2

Can f3

Can f4

Can f5

Can f6

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Testing begins with analysis of dog dander IgE. If dog dander IgE is negative (<0.10 kU/L), testing is complete.

 

If dog dander IgE is 0.10 kU/L or more, then 6 dog dander components (Can f 1, Can f 2, Can f 3, Can f 4, Can f 5, Can f 6) are performed at an additional charge.

Specimen Type
Describes the specimen type validated for testing

Serum

Ordering Guidance

For a listing of allergens available for testing, see Allergens - Immunoglobulin E (IgE) Antibodies

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.

Special Instructions
Library of PDFs including pertinent information and forms related to the test

Forms

If not ordering electronically, complete, print, and send an Allergen Test Request (T236) with the specimen.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

0.7 mL

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Gross hemolysis OK
Gross lipemia OK
Gross icterus OK

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 14 days
Frozen 90 days

Useful For
Suggests clinical disorders or settings where the test may be helpful

Evaluating patients with suspected dog dander allergy

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Testing begins with analysis of dog dander IgE. If dog dander IgE is negative (<0.10 kU/L), testing is complete.

 

If dog dander IgE is 0.10 kU/L or more, then 6 dog dander components (Can f 1, Can f 2, Can f 3, Can f 4, Can f 5, Can f 6) are performed at an additional charge.

Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Dog (canine) dander allergy is one of the most common epidermal allergies in the United States, with an estimated prevalence of sensitization of approximately 10%. Overall, allergies to dogs and cats may afflict up to 20% of the world’s population, and the prevalence appears to be increasing over time. The assessment of dog allergen-related sensitivity and allergy is dependent upon the presence of compatible clinical symptoms in the context of exposure, with support from identification of potential canine-specific IgE allergen antibodies either by skin testing or in vitro serology testing.

 

There is a correlation between elevated total dog (canine) IgE allergen antibodies and an increased likelihood of a clinical allergic response. Once an elevated antibody response to total dog dander IgE extract is established, assessment for the presence of specific IgE antibodies to the most common dog allergenic components will be performed, which can yield additional, potentially useful information for clinical assessment of dog allergy and sensitization. During dog component allergen IgE antibody testing, the presence of IgE antibodies specific for potentially allergenic individual proteins, namely Can f 1, Can f 2, Can f 3, Can f 4, Can f 5, and Can f 6, are individually assessed. The determination of the relative amount of IgE antibody to specific dog components can aid in assessment of the potential strength and type of allergenic response. However, the correlation between total serum IgE testing and skin testing is not ideal, with estimates of 52% concordance. In vitro testing has generally focused on assessing for the presence of total IgE serum antibodies to total dog allergen extracts and has overall estimated sensitivities of 75% in symptomatic individuals.

 

Canis familiaris allergen 1 (Can f 1) is a major allergen and is a salivary lipocalin protein found in all homes with dogs. Particles containing Can f 1 can remain airborne and can be inhaled. Several studies have demonstrated that approximately half of the individuals with dog allergies have IgE antibodies directed exclusively to the Can f 1 component. Increasing IgE antibody concentrations against lipocalins, such as Can f 1, correlates with the severity of asthma. Sensitization to Can f 1 in childhood was significantly associated with symptoms to dog allergy at age 16 years, and high levels of antibodies to Can f 1 were strongly associated with asthma in a population-based study of 19 year olds. Can f 1 is the most dominant dog allergen, although only 64% of individuals who are allergic to dogs react to Can f 1. While Can f 1 can be reliably used to identify dog-allergic individuals who sensitized to Can f 1, sensitivity for detecting potential dog allergy (and allergen sensitization) increases if multiple allergen components are assayed.

 

Can f 2 is a salivary lipocalin protein and an allergen present in dog hair and dander. Sensitivity to Can f 2 is associated with high levels of bronchial inflammation and is more common among patients with severe asthma. It is believed that sensitized patients with reactivity to Can f 2 will always react to Can f 1.

 

Can f 3 is a serum albumin allergen found in dog dander, hair, epithelia, saliva, and in house dust and is considered an intermediate dog allergy component. Sensitization to Can f 3 is associated with increased risks of current asthma, current allergic rhinitis, and concomitant asthma and allergic rhinitis.(1) There is observed cross-reactivity of Can f 3 patient IgE antibodies with albumins from many species, including the cat allergen Fel d 2, which may cause sensitization.

 

Can f 4 is the most abundantly detected allergen in dog fur and a major allergen component of dog hair and dander extracts. Sensitization to the lipocalin Can f 4 is associated with asthma and serves as a marker for clinically relevant dog allergy. Assessment of antibodies to Can f 4, in combination with other dog allergens, may improve the reliability of dog allergy assessment.

 

Can f 5 is a prostatic kallikrein component of dog hair and dander produced by intact (unneutered) male dogs. Approximately two-thirds of individuals who are allergic to canines demonstrate IgE reactivity to Can f 5. Additionally, a substantial proportion of those individuals are monosensitized to Can f 5 and react specifically to intact male dogs rather than female dogs or castrated male dogs. Sensitization to Can f 5 is associated with asthma and rhinoconjunctivitis symptoms and can contribute to polysensitization in individuals with IgE responses to multiple animal allergen molecules. Due to cross-reactivity with prostate-specific antigen of human seminal plasma, sensitization to Can f 5 may also contribute to the occurrence of human sexual disorders, including infertility.

 

Can f 6 is a major dog allergen present in dog dander. Sensitization to Can f 6 is associated with dog-related rhinitis and asthma. Can f 6 shares extensive cross-reactivity with other mammalian lipocalins, particularly cat and horse, and thus contributes to multi-animal allergic sensitization and potential resulting clinical respiratory symptoms.

 

Polysensitization to multiple allergens should be considered during the evaluation of dog component assay results. In a study of 75 patients with clinical allergy, the majority exhibited IgE antibodies reactive with Can f 1 and Can f 2. Asthma and decreased lung function were most strongly associated with sensitization to a group of 27 components, including Can f 1, Can f 2, and Can f 3. Polysensitization to 3 or more allergen molecules from dogs was a better predictor of dog allergy-related symptoms than results of IgE antibody tests utilizing total dog allergen extracts. Most dog-sensitized children are reactive to more than one dog allergen component, with co-sensitization to Can f 5 and Can f 1/Can f 2 conferring higher asthma risks. Reducing canine exposure should be considered if co-reactivity to these components is present.

 

Table. Specific Dog Allergens

Allergen

Most common reaction type

Selected potential cross-reactivity with other allergens

Can f1 (lipocalin)

 

One of the major dog component allergens.

For individuals with clinical allergy symptoms to dogs, approximately half show antibody reactivity to Can f 1.

Increased severity of asthma symptoms

Some cross-reactivity with cat component Fel d7, which is a lipocalin

Can f2

(lipocalin)

Bronchial inflammation

-Sensitivity to Can f 2 is associated with high levels of bronchial inflammation and is more common among patients with severe asthma.

-Sensitized patients with reactivity to Can f 2 will also react to Can f 1.(2,3)

Can f 1, limited cross-reactivity with Fel d 4

Can f3

(serum albumin)

Sensitization to Can f 3 is associated with increased risks of asthma and allergic rhinitis.

Serum albumins are a minor allergen in animal dander but can play a significant role as cross-reacting allergens.

Antibodies against this component may indicate cross-reactivity associated with albumins from humans, pigs, cattle, cats (Fel d2), sheep, horses, mice, and rats.

Can f4

(lipocalin)

Asthma

-Sensitization to lipocalins such as Can f 4 are associated with asthma

-Can f 4 is considered a major allergen component of dog dander

Minor cross-reactivity with Can f1, Can f2, Equ c1, Fel d4

Can f5

(kallikrein)

Asthma, rhinoconjunctivitis symptoms

-In the absence of other component sensitization, there may be reduced/absent allergic symptoms in the presence of female or neutered male dogs.

Same protein family as cows, horses, rats, rabbits, mice, and guinea pigs.

 

There is no observed cross-reactivity between Can f 5 and Can f 1, Can f 2, or Can f 3 (1). Can f 5 cross-reacts with prostate-specific antigen (PSA) of human seminal plasma

Can f6

(lipocalin)

Dog-related rhinitis and asthma

Can f 6 lipocalin sensitized individuals may also react to horse and cat lipocalins. This can be responsible for co-sensitization among these animals.

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

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

> or =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
Provides information to assist in interpretation of the test results

When detectable total dog dander IgE antibody is present (> or =0.10 IgE kUa/L), additional specific component IgE antibody testing will be performed. If at least one potential specific allergenic dog dander component IgE is detectable (> or =0.10 IgE kUa/L), an interpretative report will be provided.

 

When the sample is negative for total dog dander IgE antibody (<0.10 IgE kUa/L), additional testing for specific dog component IgE antibodies will not be performed. Negative IgE results for total dog dander antibody may indicate a lack of sensitization to potential dog allergenic components.

Cautions
Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Clinical correlation of results from in vitro IgE testing with patient history of allergic or anaphylactic responses to dogs is recommended.

-Negative results for IgE to total dog dander and any dog allergenic components do not completely exclude the possibility of clinically relevant allergic responses upon exposure to dog dander.

-Positive results for IgE to total dog dander or any potential dog allergenic components are not diagnostic for dog allergy and only indicate patient may be sensitized to dog 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 the 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.

Clinical Reference
Recommendations for in-depth reading of a clinical nature

1. Mattsson L, Lundgren T, Everberg H, et al: Prostatic kallikrein: a new major dog allergen. J Allergy Clin Immunol. 2009 Feb;123(2):362-368

2. Davila I, Dominguez-Ortega J, Navarro-Pulido A, et al: Consensus document on dog and cat allergy. Allergy. 2018 Jun;73(6):1206-1222. doi: 10.1111/all.13391

3. Nilsson OB, Binnmyr J, Zoltowska A, Saarne T, van Hage M, Gronlund H: Characterization of the dog lipocalin allergen Can f 6: the role in cross-reactivity with cat and horse. Allergy. 2012;67(6):751-757

4. Konieczny A, Morgenstern JP, Bizinkauskas CB, et al: The major dog allergens, Can f 1 and Can f 2, are salivary lipocalin proteins: cloning and immunological characterization of the recombinant forms. Immunology. 1997;92(4):577-586

5. Schou C, Svendsen UG, Lowenstein H: Purification and characterization of the major dog allergen, Can f I. Clin Exp Allergy. 1991;21(3):321-328

6. Bjerg A, Winberg A, Berthold M, Mattsson L, Borres MP, Ronmark E: A population-based study of animal component sensitization, asthma, and rhinitis in schoolchildren. Pediatr Allergy Immunol. 2015 Sept;26(6):557-563

7. Konradsen JR, Fujisawa T, van Hage M, et al: Allergy to furry animals: New insights, diagnostic approaches, and challenges. J Allergy Clin Immunol. 2015;135(3):616-625

8. Spitzauer S, Pandjaitan B, Soregi G, et al. IgE cross-reactivities against albumins in patients allergic to animals. J Allergy Clin Immunol. 1995;96(6 Pt 1):951-959

9. Chruszcz M, Mikolajczak K, Mank N, Majorek KA, Porebski PJ, Minor W: Serum albumins-unusual allergens. Biochim Biophys Acta. 2013;1830(12):5375-5381

10. Nwaru BI, Suzuki S, Ekerljung L, et al: Furry animal allergen component sensitization and clinical outcomes in adult asthma and rhinitis. J Allergy Clin Immunol Pract. 2019;7(4):1230-1238.e4

11. Schoos AM, Kattan JD, Gimenez G, Sampson HA: Sensitization phenotypes based on protein groups and associations to allergic diseases in children. J Allergy Clin Immunol. 2016 Apr;137(4):1277-1280

12. Rytkonen-Nissinen M, Saarelainen S, Randell J, Hayrinen J, Kalkkinen N, Virtanen T. IgE reactivity of the dog lipocalin allergen Can f 4 and the development of a sandwich ELISA for its quantification. Allergy Asthma Immunol Res. 2015 Jul;7(4):384-392

13. Schoos AM, Bonnelykke K, Chawes BL, Stokholm J, Bisgaard H, Kristensen B: Precision allergy: Separate allergies to male and female dogs. J Allergy Clin Immunol Pract. 2017 Nov-Dec;5(6):1754-1756

14. Basagana M, Bartolome B, Pastor-Vargas C, Mattsson L, Lidholm J, Labrador-Horrillo M: Involvement of Can f 5 in a case of human seminal plasma allergy. Int Arch Allergy Immunol. 2012;159(2):143-146

15. Chan SK, Leung DYM: Dog and cat allergies: Current state of diagnostic approaches and challenges. Allergy Asthma Immunol Res. 2018 Mar;10(2):97-105. doi: 10.4168/aair.2018.10.2.97

16. Salo PM, Arbes SJ Jr, Jaramillo R, et al: Prevalence of allergic sensitization in the United States: results from the National Health and Nutrition Examination Survey (NHANES) 2005-2006. J Allergy Clin Immunol. 2014 Aug;134(2):350-359. doi: 10.1016/j.jaci.2013.12.1071

Method Description
Describes how the test is performed and provides a method-specific reference

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)

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday through Friday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

Same day/1 to 3 days

Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

Rochester

Fees
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Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

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
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

86003

LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
DOGPF Dog Dander Component Reflex, S 6098-8
Result Id Test Result Name Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
DOGD1 Dog Dander, IgE, S 6098-8

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | PHP Pdf | CMS Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports