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在欧洲“PRECISESADS”项目的背景下,对流式细胞仪进行多中心协调。

Multi-center harmonization of flow cytometers in the context of the European "PRECISESADS" project.

机构信息

INSERM ERI29, EA2216, Université de Brest, Labex IGO, CHRU Morvan, Brest, France.

INSERM ERI29, EA2216, Université de Brest, Labex IGO, CHRU Morvan, Brest, France.

出版信息

Autoimmun Rev. 2016 Nov;15(11):1038-1045. doi: 10.1016/j.autrev.2016.07.034. Epub 2016 Aug 1.

Abstract

The innovative medicine initiative project called PRECISESADS will study 2.500 individuals affected by systemic autoimmune diseases (SADs) and controls. Among extensive OMICS approaches, multi-parameter flow cytometry analyses will be performed in eleven different centers. Therefore, the integration of all data in common bioinformatical and biostatistical investigations requires a fine mirroring of all instruments. We describe here the procedure elaborated to achieve this prerequisite. One flow cytometer chosen as reference instrument fixed the mean fluorescence intensities (MFIs) of 8 different fluorochrome-conjugated antibodies (Abs) using VersaComp Ab capture beads. The ten other centers adjusted their own PMT voltages to reach the same MFIs. Subsequently, all centers acquired Rainbow 8-peak beads data on a daily basis to follow the stability of their instrument overtime. One blood sample has been dispatched and concomitantly stained in all centers. Comparison of leukocytes frequencies and cell surface marker MFIs demonstrated the close sensitivity of all flow cytometers, allowing a multicenter analysis. The effective multi-center harmonization enables the constitution of a workable wide flow cytometry database for the identification of specific molecular signatures in individuals with SADs.

摘要

名为 PRECISESADS 的创新药物倡议项目将研究 2500 名受系统性自身免疫性疾病(SAD)和对照组影响的个体。在广泛的 OMICS 方法中,将在十一个不同的中心进行多参数流式细胞术分析。因此,所有数据的综合分析需要在共同的生物信息学和生物统计学研究中进行精细的仪器匹配。我们在这里描述了为实现这一前提条件而制定的程序。一台选定为参考仪器的流式细胞仪使用 VersaComp Ab 捕获珠固定了 8 种不同荧光素标记抗体(Abs)的平均荧光强度(MFI)。其他十个中心调整了自己的 PMT 电压,以达到相同的 MFI。随后,所有中心每天都采集 Rainbow 8-peak 珠数据,以跟踪仪器随时间的稳定性。一个血样被分发给所有中心并同时染色。白细胞频率和细胞表面标志物 MFI 的比较表明,所有流式细胞仪的灵敏度都很高,允许进行多中心分析。有效的多中心协调使我们能够建立一个可行的广泛流式细胞术数据库,以识别 SAD 个体中的特定分子特征。

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