通过流式细胞术实现外周血调节性 T 细胞检测标准化的性能验证方法。

Mei Liu, Jin-Peng Liu, Pan Wang, Ya-Jing Fu, Min Zhao, Yong-Jun Jiang, Zi-Ning Zhang, Hong Shang
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引用次数: 0

摘要

背景基于流式细胞术检测外周血中的调节性 T 细胞 (Treg) 对于诊断和治疗免疫介导疾病非常重要。然而,目前缺乏可靠的方法来验证其性能,而这对 Tregs 检测的标准化至关重要:基于流式细胞术和不同试剂盒 Treg 检测的一致性分析,开展标准化研究并验证 3 种市售 Tregs 检测试剂盒的性能:设计: 在确定了门控策略和最佳抗体浓度之后,使用 3 家生产商提供的试剂盒对 Tregs 检测的分析性能进行了评估。评估了采集后样本的稳定性、重复性、再现性、可报告范围、线性度和测定携带率。通过Bland-Altman图和线性回归分析评估了不同检测方法之间的一致性。评估了 CD4+CD25+CD127low/- Tregs 和 CD4+CD25+Foxp3+ Tregs 频率之间的关系:样品采集后的稳定性定为室温下采集后 72 小时。准确度、重复性、再现性和精确度均符合临床分析的要求。线性度极佳,R2 ≥0.9,且无测定携带。就可报告范围而言,Tregs 检测要求 CD3+CD4+ 门至少有 1000 个事件。此外,3 家生产商的抗体标记 Tregs 的结果非常一致。CD4+CD25+CD127low/- Tregs的百分比与CD4+CD25+Foxp3+ Tregs密切相关:这是第一项通过流式细胞术系统评估外周血中 Tregs 测量性能的研究,为验证基于流式细胞术的免疫监测项目在临床实践中的性能提供了实用的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Approaches for Performance Verification Toward Standardization of Peripheral Blood Regulatory T-Cell Detection by Flow Cytometry.

Context.—: Regulatory T-cell (Treg) detection in peripheral blood, based on flow cytometry, is invaluable for diagnosis and treatment of immune-mediated diseases. However, there is a lack of reliable methods to verify the performance, which is pivotal towards standardization of the Tregs assay.

Objective.—: To conduct standardization studies and verify the performance of 3 commercially available reagent sets for the Tregs assay based on flow cytometry and agreement analysis for Treg detection across the different reagent sets.

Design.—: The analytical performance of Tregs assay using reagent sets supplied by 3 manufacturers was evaluated after establishing the gating strategy and determining the optimal antibody concentration. Postcollection sample stability was evaluated, as well as the repeatability, reproducibility, reportable range, linearity, and assay carryover. Agreement between the different assays was assessed via Bland-Altman plots and linear regression analysis. The relationship between the frequency of CD4+CD25+CD127low/- Tregs and CD4+CD25+Foxp3+ Tregs was evaluated.

Results.—: The postcollection sample stability was set at 72 hours after collection at room temperature. The accuracy, repeatability, reproducibility, and accuracy all met the requirements for clinical analysis. Excellent linearity, with R2 ≥0.9 and no assay carryover, was observed. For reportable range, a minimum of 1000 events in the CD3+CD4+ gate was required for Tregs assay. Moreover, the results for Tregs labeled by antibodies from the 3 manufacturers were in good agreement. The percentage of CD4+CD25+CD127low/- Tregs was closely correlated with CD4+CD25+Foxp3+ Tregs.

Conclusions.—: This is the first study to evaluate systematically the measurement performance of Tregs in peripheral blood by flow cytometry, which provides a practical solution to verifying the performance of flow cytometry-based immune monitoring projects in clinical practice.

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