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比较同日和延迟检测结核特异性 T 细胞应答。

Comparison of same day versus delayed enumeration of TB-specific T cell responses.

机构信息

Lung Infection and Immunity Unit, Division of Pulmonology & UCT Lung Institute, University of Cape Town, Department of Medicine, H floor, Old Main Building, Groote Schuur Hospital, Observatory, Cape Town 7925, South Africa.

出版信息

J Infect. 2010 May;60(5):344-50. doi: 10.1016/j.jinf.2010.01.012. Epub 2010 Feb 10.

Abstract

BACKGROUND/OBJECTIVE: Flexibility in sample processing may improve test utility of the quantitative antigen-specific T cell assay (T-SPOT.TB). We investigated whether delayed sample processing with and without the use of T-Cell Xtend, a proprietary reagent, impacted upon test accuracy.

METHODS

Blood samples obtained from 363 sequentially recruited tuberculosis suspects or treated patients were processed immediately (day 0) and at different times after receipt of the sample [approximately 24-h (day 1) or approximately 32-h (day 2)] with and without adding T-Cell Xtend.

RESULTS

T-Cell-Xtend-independent median ELISPOT counts (spot forming cells per million peripheral blood mononuclear cells) were significantly higher at day 1 versus day 0 (114 vs. 100; n=66; p=0.03); inter-time-point agreement between the results was 95.45% and the conversion/reversion rate was 4.55%. By contrast, counts on day 0 without T-Cell Xtend versus day 1 with T-Cell Xtend were similar (56 vs. 56; n=215), inter-time-point agreement between the results was 97.17%, and the conversion/reversion rate was 2.83%. Counts performed at day 2 with T-Cell Xtend were not significantly different from day 0. These findings were independent of HIV status.

CONCLUSION

There was high agreement between results when samples were processed immediately and after a 24-h delay. However, although the use of T-Cell Xtend appeared to reduce the number of conversions/reversions this reduction was not statistically significant. Larger studies are required to clarify these findings.

摘要

背景/目的:样本处理的灵活性可能会提高定量抗原特异性 T 细胞检测(T-SPOT.TB)的检测效能。我们研究了在接收样本后是否延迟处理样本(分别在 24 小时[第 1 天]和 32 小时[第 2 天])以及是否使用 T 细胞扩展试剂(一种专利试剂)是否会影响检测的准确性。

方法

对 363 例连续招募的结核病疑似患者或治疗患者的血液样本进行即时处理(第 0 天)和延迟处理(在接收样本后约 24 小时[第 1 天]或约 32 小时[第 2 天]),处理时添加和不添加 T 细胞扩展试剂。

结果

在不添加 T 细胞扩展试剂的情况下,第 1 天的 ELISPOT 计数(每百万外周血单核细胞中的斑点形成细胞)中位数明显高于第 0 天(114 对 100;n=66;p=0.03);两个时间点之间的结果一致性为 95.45%,转换/反转率为 4.55%。相比之下,在添加 T 细胞扩展试剂的情况下,第 0 天和第 1 天的计数结果相似(56 对 56;n=215),两个时间点之间的结果一致性为 97.17%,转换/反转率为 2.83%。在添加 T 细胞扩展试剂的情况下,第 2 天的计数结果与第 0 天无明显差异。这些发现与 HIV 状态无关。

结论

样本即时处理和延迟 24 小时处理后,结果具有高度一致性。然而,尽管使用 T 细胞扩展试剂似乎减少了转换/反转的数量,但这种减少在统计学上并不显著。需要更大的研究来澄清这些发现。

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