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Short-Term Reproducibility of a Commercial Interferon Gamma Release Assay
Author(s) -
Anne Detjen,
Laurianne Loebenberg,
Harleen M. S. Grewal,
Kim Stanley,
Andrea Gutschmidt,
Clarissa Kruger,
Nelita du Plessis,
Martin Kidd,
Nulda Beyers,
Gerhard Walzl,
Anneke C. Hesseling
Publication year - 2009
Publication title -
clinical and vaccine immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.649
H-Index - 77
eISSN - 1556-6811
pISSN - 1556-679X
DOI - 10.1128/cvi.00168-09
Subject(s) - reproducibility , interferon gamma release assay , mycobacterium tuberculosis , interferon gamma , medicine , intraclass correlation , tuberculosis , quantiferon , immunology , immune system , statistics , pathology , latent tuberculosis , mathematics
Interferon gamma release assays (IGRAs) have been shown to be sensitive and highly specific for the detection of immune memory againstMycobacterium tuberculosis . Little is known about the reproducibility and within-person variability of these assays. Various aspects of short-term reproducibility of a commercial IGRA, the QuantiFERON-TB Gold In-Tube (QFT-IT) assay, were assessed. The QFT-IT assay was performed twice within 3 days in 27 health care workers in Cape Town, South Africa. Two sets of tests were performed by different operators on day 1, and one set was performed on day 3. Aspects such as interoperator, intraoperator, day-to-day variability, and test-retest variability as well as different the storage methods of plasma were investigated. Seventeen of 27 (63%) of participants had at least one positive QFT-IT text; six had discordant results. The agreement of all aspects studied was high, with kappa values between 0.82 and 1.00 for dichotomous measures, and interclass correlations (ICC) of 0.809 to 0.965 were observed for continuous gamma interferon (IFN-γ) measures. The variability of the magnitude of response was highest comparing measures obtained from individuals on different days (ICC of 0.809). The magnitude of the IFN-γ responses between assays performed for individual participants was variable, with ranges from 0.03 to 11 IU/ml, resulting is discordant results for five participants. The results indicate that the QFT-IT assay is a robust and highly reproducible assay. Considerable intraindividual variability occurs in the magnitude of IFN-γ responses, which may influence the interpretation of serial measures.

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