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Allergen Specific IgE

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Test Background

Specific IgE tests (previously known as a RAST): These tests are for the investigation of IgE mediated hypersensitivity (allergic) reactions. Specific IgE testing should be targeted only at triggers (aeroallergens/venom/food/drugs) of immediate hypersensitivity (urticaria, angioedema, pruritus, wheeze) identified by a thorough clinical history. The laboratory does not recommend the testing of more than 10 allergens per patient.

A positive specific IgE result does not confirm allergy, only sensitisation to the allergen in question. These tests can help to confirm a diagnosis of an allergic disorder in patients with a clinical history consistent with an immediate allergic reaction. They are particularly useful when skin testing cannot or should not be performed (dermatographism, extensive eczema, patients unable to stop anti-histamines or tricyclic anti-depressant medication). All patients with anaphylaxis should be referred to an allergy clinic according to NICE guidance.

False positive specific IgE results can occur in patients with high total IgE levels (IgE >1000 KUA/L). Low level positive specific IgE results in these patients should be interpreted with caution. A negative specific IgE does not exclude IgE mediated allergy where there is a convincing clinical history.

Aeroallergen IgE Testing: Common aeroallergens in the UK include grass, tree, weed pollens, house dust mite, cat and dog dander and fungal spores. IgE testing is recommended for the diagnosis of allergic rhinitis which affects up to 20% of UK adults. Pollen sensitisation can lead to the pollen food allergy syndrome which can often be diagnosed on clinical history alone.

Food Allergy IgE Testing: Indiscriminate specific IgE testing is strongly discouraged due to the limited specificity of food IgE tests and their potential to promote anxiety, the unnecessary elimination of food leading to nutritional and growth disorders and reduced quality of life. Unnecessary elimination diets can induce allergic disease including anaphylaxis to previously tolerated foods. Symptoms (urticaria, angioedema, eczema flares) that have no close temporal association to food (onset at night or early morning more than 2 hours after food has been consumed) are unlikely to be IgE mediated. Atypical presentations and reactions following composite meals should be referred to an Allergy clinic. In all cases only food reported to provoke symptoms should be tested. The laboratory recommends testing a maximum of 10 food allergens per patients.

Drug IgE Testing: The laboratory does not recommend penicillin IgE testing within primary care. This test has limited sensitivity and specificity for penicillin allergy and clinicians are advised to first use the PEN-FAST tool for assessment of penicillin allergy risk.

Component resolved IgE testing: The laboratory also offers component resolved diagnostics (CRD). These tests detect IgE to specific components of an allergen. CRD is useful in delineating pollen food syndrome from primary food sensitisation, for the confirmation of LTP sensitisation and for the selection and monitoring of oral immunotherapy.

Specific IgE testing is performed by fluoroenzymeimmunoassay (Immunocap) on Phadia.

Clinical Indications

Investigation of type 1 hypersensitivity (allergic) reactions where skin testing is contraindicated.
Selection of patients for immunotherapy.

Reference Range

<0.35 kUA/L (Measurement range 0.1 – 100 kAU/L)

This range originates from the detection limit of the first assays available, new assays now have lower detection limits and some patients will react to an allergen when specific IgE is low (0.10—0.34kUA/L). A positive result does not indicate allergy, only the potential to react to an allergen and the magnitude of a sIgE result does not correlate with clinical severity, only to the likelihood of clinical reactivity to the allergen in question.

Defined cut offs where the probability of clinical allergy is very high have been described for some foods, e.g. peanut >15 kUA/L (BSACI 2017).

 

 

Sample volume
5-10 mL blood (1 mL serum)
Turnaround time
14 days (Referred Tests Up To 21 Days)
Sample & Container Required
Serum (rust top RST tube or yellow top tube)
Notes

Rare allergens not tested by the laboratory are referred.

Referral Laboratory: Biomnis/Eurofins Laboratories, Lyons, France.

The Laboratory is currently unaccredited for all specific IgE Allergy tests, including allergen components due to a change in platform.

Information and advice for GPs about the use of IgE blood tests and changes to the IgE testing process and interpretative reports:

Allergy Testing Update

Advice on diagnosis and assessment of food allergic disorders

Food Allergy Syndromes

Penicillin Allergy

Accreditation

This test is not currently accredited

Record last updated
January 2, 2026

Sample Container

5ml RST Vacutainers (Rust top)

Sample Container

5ml SST Vacutainers (Gold / Yellow top)

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Test Results

Yes, we have a Pathology User Guide

Yes. Please email your request to Imperial.nwlpcustomerservice@nhs.net

Results are communicated to clinical staff and are normally not communicated direct to patients either on telephone requests or in written report. If you need to contact us please click here to view the contact details page

Please contact the Customer Service Team Monday to Friday from 8:30am – 6:00pm on 0203 313 5353. Alternatively, see the Pathology User Guide for how to contact the relevant department. If advice is not urgent you can also email your query to Imperial.nwlpcustomerservice@nhs.net

Additional tests may be added by discussion with the relevant laboratory. The time limit for adding additional tests to a sample already received in the laboratory will depend on the type of sample and the department it was sent to.

Information on the repertoire of tests performed by pathology, including reference ranges, turnaround times and specimen requirements, can be found in the test directory.

NWLP operates UKAS accredited medical laboratories as per the references below. The current scope of accreditation for all NWLP’s laboratories can be found on the UKAS website.

See the following UKAS ref numbers:

  • Clinical Biochemistry Ref: 8673
  • Haematology and Blood Transfusion Ref: 8674
  • Infection & Immunity Sciences (Including Immunology, Virology, Microbiology and Histocompatibility and Immunogenetics ) Ref: 8659
  • Cellular Pathology (Including Histopathology, Cytology and Molecular Pathology) Ref: 9615

If you require copies of our certificate of accreditation and associated documentation please contact Imperial.nwlpcustomerservice@nhs.net.

UKAS requires the laboratories to be accredited for a particular repertoire/scope (ISO15189), any changes or additions to repertoire require assessment by UKAS (extension to scope).

The BD Hospital Tube GuideBD GP Tube Guide and BD Paediatric Tube Guide provide visual references to the correct tube types and collection instructions.

Home testing

INSTRUCTION SHEET FOR BLOOD SAMPLE COLLECTION 

We also have two instruction videos available (one with subtitles and one without) – please click on the links to view the videos on Google.

VIDEO ON BLOOD SAMPLE COLLECTION (without subtitles)

VIDEO ON BLOOD SAMPLE COLLECTION (with subtitles)

Our accreditations

Upholding excellence in diagnostic standards

Our laboratories are accredited by the UK Accreditation Service (UKAS) against the international standard ISO15189:2022. UKAS is the accreditation body for the UK that assesses medical laboratories.

Find out more about our accreditations on the UKAS website.

UKAS website
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