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免疫监测方法在临床研究中的验证:HLA-肽三聚体染色分析。

Validation of Immunomonitoring Methods for Application in Clinical Studies: The HLA-Peptide Multimer Staining Assay.

机构信息

Department of Immunology, Institute for Cell Biology, Eberhard Karls University, and German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ) Partner Site Tuebingen, Tuebingen, Germany.

Cancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, SO16 6YD, United Kingdom.

出版信息

Cytometry B Clin Cytom. 2018 Mar;94(2):342-353. doi: 10.1002/cyto.b.21397. Epub 2016 Jul 22.

Abstract

BACKGROUND

Validated assays are essential to generate data with defined specificity, consistency, and reliability. Although the process of validation is required for applying immunoassays in the context of clinical studies, reports on systematic validation of in vitro T cell assays are scarce so far. We recently validated our HLA-peptide multimer staining assay in a systematic manner so as to qualify the method for monitoring antigen-specific T cell responses after immunotherapy.

METHODS

Parameters of the assay, specificity, precision, linearity, sensitivity, and robustness were assessed systematically. Experiments were designed to address specifically each parameter and are detailed.

RESULTS

Nonspecific multimer staining was below the acceptance limit of 0.02% multimer CD8 cells. The assay showed acceptable precision in all dimensions it was repeated (CV < 10%) and also demonstrated a linear detection (R  > 0.99) of antigen specific cells.

CONCLUSIONS

We succeeded in validating the HLA-multimer staining assay in a systematic manner. Additionally, we propose a technical framework and recommendations that can be applied for validating other T cell assessment methods. © 2016 International Clinical Cytometry Society.

摘要

背景

为了生成具有明确特异性、一致性和可靠性的数据,验证检测方法至关重要。尽管免疫分析在临床研究中的应用需要经过验证过程,但到目前为止,关于体外 T 细胞分析的系统验证报告还很少。我们最近以系统的方式验证了我们的 HLA 肽多聚体染色分析,以确定该方法用于监测免疫治疗后抗原特异性 T 细胞反应的适用性。

方法

系统评估了检测方法的参数、特异性、精密度、线性、灵敏度和稳健性。设计了专门的实验来解决每个参数,并详细说明了实验设计。

结果

非特异性多聚体染色低于 0.02%多聚体 CD8 细胞的可接受限值。该分析在所有重复的维度上都具有可接受的精密度(CV<10%),并且还证明了抗原特异性细胞的线性检测(R>0.99)。

结论

我们成功地以系统的方式验证了 HLA 多聚体染色分析。此外,我们提出了一个技术框架和建议,可用于验证其他 T 细胞评估方法。©2016 年国际临床细胞分析学会。

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