The Performance of the Agility System for Interferon Gamma Release Assay Using QuantiFERON TB Gold In-Tube Assay
Background: As stated in ‘The Action Strategy for Tuberculosis-Free Korea,’ last March, high-throughput, large-scale analytical instruments for interferon gamma release assays (IGRA) are demanded by many clinical laboratories using the QuantiFERON-TB Gold In- Tube assay (Cellestis/Qiagen, Australia)...
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Published in | Imsang byeong'ri wa jeongdo gwanri/Journal of laboratory medicine and quality assurance Vol. 41; no. 1; pp. 29 - 38 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
대한임상검사정도관리협회
31.03.2019
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Subjects | |
Online Access | Get full text |
ISSN | 2384-2458 1225-097X 2288-7261 2288-7261 |
DOI | 10.15263/jlmqa.2019.41.1.29 |
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Summary: | Background: As stated in ‘The Action Strategy for Tuberculosis-Free Korea,’ last March, high-throughput, large-scale analytical instruments for interferon gamma release assays (IGRA) are demanded by many clinical laboratories using the QuantiFERON-TB Gold In- Tube assay (Cellestis/Qiagen, Australia). Agility (Dynex Technologies, USA) is an automated high-throughput enzyme linked immunosorbent assay analyser. The present study aimed to evaluate its accuracy and speed.
Methods: Pooled plasma was prepared using samples obtained after IGRA testing. Analyses of precision, linearity, cut-off evaluation, and comparison with conventional methods were performed for multiple Agility instruments according to the Clinical and Laboratory Standards Institute EP5-A3, EP6-A, EP9-A3 and EP12-A2 guidelines. The turnaround time and throughput were also analysed.
Results: The coefficient of variation range was 2.48%–4.0%, 7.01%–11.17%, and 9.69%– 14.84% for the repeatability, between-run precision, and between-day precision analyses, respectively. The linearity ranged from 0 to 10.541. Comparison analysis presented a high concordance of Agility with the conventional instrument, DS2 (Dynex Technologies), and manual method for IGRA. The cut-off value of 0.35 IU/mL was well compatible with the C50.
It was identified that the C50±20% contained the C5–C95 interval. The average turnaround time was 3.84 hours, from the submission of pre-treated samples to the reporting of results.
The throughput was determined to be 290 tests during a routine working time of 8 hours.
Conclusions: Agility showed high precision, linearity, concordance, and had a 2.5 times faster throughput than with the conventional and manual method. It could be useful for large-scale IGRA testing in latent tuberculosis infection screening project. Samples within C50±20% are suspected to show relatively low reporducible results of high inversion between postivie and negative. KCI Citation Count: 0 |
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ISSN: | 2384-2458 1225-097X 2288-7261 2288-7261 |
DOI: | 10.15263/jlmqa.2019.41.1.29 |