Korean J Lab Med.  2006 Oct;26(5):362-368. 10.3343/kjlm.2006.26.5.362.

Evaluation of Allergen Specific IgE assay on ADVIA Centaur Immunoassay System

Affiliations
  • 1Department of Laboratory Medicine, Bundang Jesaeng General Hospital, Sungnam, Korea. hskim@dmc.or.kr
  • 2Department of Otorhinolaryngology, Bundang Jesaeng General Hospital, Sungnam, Korea.
  • 3Department of Pulmonology and Allergy, Bundang Jesaeng General Hospital, Sungnam, Korea.
  • 4Department of Dermatology, Bundang Jesaeng General Hospital, Sungnam, Korea.
  • 5Department of Pediatrics, Bundang Jesaeng General Hospital, Sungnam, Korea.

Abstract

BACKGROUND: Allergen specific IgE (sIgE) assay is an important aid in the diagnosis and treatment of allergy. We evaluated the analytical performance of a quantitative chemiluminescence immunoassay for sIgE using the continuous random access ADVIA Centaur.
METHODS
Six ADVIA Centaur sIgE reagents for common inhalant allergens in Korea, d1, d2, e1, e5, t3, and t7, were evaluated for precision, dilution recovery (parallelism), comparison with Pharmacia UniCAP sIgE assay and skin prick test, sample volume, and analytical speed according to the NCCLS guidelines (I/LA20-A, EP5-A2). Commercialized positive and negative quality control materials were used for a precision study, and samples from a total of 110 patients were used for dilution recovery and comparison studies.
RESULTS
Within-run coefficients of variation (CV) of the 6 items were 3.45-6.14% and within-device CVs (total CVs) of all items were below 10%. Interdilutional CVs of all items were 2.84-11.95%, which showed a good linearity and parallelism over its measuring range. Positive/negative concordance rates of the 6 items with UniCAP sIgE assay were 76.3-96.1% (d1, 88.2%; d2, 96.1%; e1, 91.0%; e5, 77.0%; t3, 90.5%; and t7, 76.3%). Concordance rates of the six items with skin prick test were all above 80%. The quantity of sample volume (25 micro L/test) needed was relatively small, and a high throughput (120 tests/hr) and rapid turnaround time (47 min) could be achieved.
CONCLUSIONS
The ADVIA Centaur sIgE assay was thought to be a convenient and efficient method to be used in medium- to large-sized laboratories.

Keyword

Allergy; specific IgE; ADVIA Centaur; evaluation

MeSH Terms

Allergens
Diagnosis
Humans
Hypersensitivity
Immunoassay*
Immunoglobulin E*
Indicators and Reagents
Korea
Luminescence
Quality Control
Skin
Allergens
Immunoglobulin E
Indicators and Reagents

Figure

  • Fig. 1. Dilution-recovery analysis for the ADVIA Centaur sIgE assay. D1, house dust mite, Dermatophagoides pteronyssinus; D2, house dust mite, Dermatophagoides farinae; E1, Cat Dander, Felis domesticus; E5, Dog dander, Canis familaris; T3, Birch, Betula verrucosa; T7, White oak, Quercus alba.

  • Fig. 2. Comparison studies between ADVIA Centaur sIgE assay and Pharmacia CAP system for 6 different allergens. The detection limit (0.35 kU/L) is shown by a solid line. D1, house dust mite, Dermatophagoides pteronyssinus; D2, house dust mite, Dermatophagoides farinae; E1, Cat Dander, Felis domesticus; E5, Dog dander, Canis familaris; T3, Birch, Betula verrucosa; T7, White oak, Quercus alba.


Reference

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