Veerapathran Anandharaman, Joshi Rajnish, Goswami Kalyan, Dogra Sandeep, Moodie Erica E M, Reddy M V R, Kalantri Shriprakash, Schwartzman Kevin, Behr Marcel A, Menzies Dick, Pai Madhukar
Department of Biochemistry, Mahatma Gandhi Institute of Medical Sciences, Sevagram, Maharashtra, India.
PLoS One. 2008 Mar 26;3(3):e1850. doi: 10.1371/journal.pone.0001850.
Although interferon-gamma release assays (IGRA) are promising alternatives to the tuberculin skin test, interpretation of repeated testing results is hampered by lack of evidence on optimal cut-offs for conversions and reversions. A logical start is to determine the within-person variability of T-cell responses during serial testing.
METHODOLOGY/PRINCIPAL FINDINGS: We performed a pilot study in India, to evaluate the short-term reproducibility of QuantiFERON-TB Gold In Tube assay (QFT) among 14 healthcare workers (HCWs) who underwent 4 serial QFT tests on day 0, 3, 9 and 12. QFT ELISA was repeated twice on the same sets of specimens. We assessed two types of reproducibility: 1) test-retest reproducibility (between-test variability), and 2) within-person reproducibility over time. Test-retest reproducibility: with dichotomous test results, extremely high concordance was noticed between two tests performed on the same sets of specimens: of the 56 samples, the test and re-test results agreed for all but 2 individuals (kappa = 0.94). Discordance was noted in subjects who had IFN-gamma values around the cut-off point, with both increases and decreases noted. With continuous IFN-gamma results, re-test results tended to produce higher estimates of IFN-gamma than the original test. Within-person reproducibility: when continuous IFN-gamma data were analyzed, the within-person reproducibility was moderate to high. While persons with negative QFT results generally stayed negative, positive results tended to vary over time. Our data showed that increases of more than 16% in the IFN-gamma levels are statistically improbable in the short-term.
Conservatively assuming that long-term variability might be at least twice higher than short-term, we hypothesize that a QFT conversion requires two conditions to be met: 1) change from negative to positive result, and 2) at least 30% increase in the baseline IFN-gamma response. Larger studies are needed to confirm our preliminary findings, and determine the conversion thresholds for IGRAs.
尽管干扰素-γ释放检测(IGRA)有望成为结核菌素皮肤试验的替代方法,但由于缺乏关于转换和逆转的最佳临界值的证据,重复检测结果的解读受到阻碍。一个合理的开端是确定连续检测期间T细胞反应的个体内变异性。
方法/主要发现:我们在印度进行了一项试点研究,以评估14名医护人员(HCW)中管内QuantiFERON-TB Gold检测(QFT)的短期重复性,这些医护人员在第0、3、9和12天接受了4次连续的QFT检测。对同一组标本重复进行两次QFT ELISA检测。我们评估了两种类型的重复性:1)重测重复性(检测间变异性),以及2)个体内随时间的重复性。重测重复性:对于二分法检测结果,在同一组标本上进行的两次检测之间观察到极高的一致性:在56个样本中,除2名个体外,所有样本的检测和重测结果均一致(kappa = 0.94)。在干扰素-γ值接近临界值的受试者中注意到不一致情况,既有升高也有降低。对于连续的干扰素-γ结果,重测结果往往比原始检测产生更高的干扰素-γ估计值。个体内重复性:当分析连续的干扰素-γ数据时,个体内重复性为中度至高。虽然QFT结果为阴性的人通常保持阴性,但阳性结果往往随时间变化。我们的数据表明,干扰素-γ水平在短期内增加超过16%在统计学上是不太可能的。
保守地假设长期变异性可能至少比短期变异性高两倍,我们假设QFT转换需要满足两个条件:1)从阴性结果变为阳性结果,以及2)基线干扰素-γ反应至少增加30%。需要更大规模的研究来证实我们的初步发现,并确定IGRA的转换阈值。