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意大利全国淋巴细胞免疫表型分析及流式细胞仪性能质量控制试验。

Nationwide quality control trial on lymphocyte immunophenotyping and flow cytometer performance in Italy.

作者信息

Brando B, Sommaruga E

机构信息

Renal Transplant Unit, Niguarda-Cà Granda Hospital, Milan, Italy.

出版信息

Cytometry. 1993;14(3):294-306. doi: 10.1002/cyto.990140310.

Abstract

The Italian Society for Cytometry (Gruppo Italiano di Citometria, GIC) promoted this nationwide large-scale quality control trial on cellular immunophenotyping and flow cytometer performance in 1991. The aim of this independent study was to evaluate instrument performance with calibrated fluorescence microbeads (minimum threshold for FITC, linearity, coefficients of variation and resolution indexes for fluorescence), and to correlate it to the measurement of lyophilized lymphocyte surface immunofluorescence staining with a wide spectrum of antibodies (percentage of positive cells and fluorescence mean intensity). A single send-out was made to 306 laboratories with 350 instruments throughout Italy. Each kit included anonymous vials containing premixed calibrated microbeads, lyophilized human lymphocytes and small aliquots of conjugated monoclonal antibodies, for both single FITC and double FITC/PE staining. Participants were also asked to use their own anti-CD4 monoclonal. A valid answer was returned by 209 laboratories with 221 instruments. Gating was not an assay variable. The minimum sensitivity threshold for FITC ranged from 26.6 to 11,293 MESF, with marked instrument heterogeneity as far as the relationship between FITC threshold and coefficients of variation for fluorescence was concerned. A low FITC threshold also correlated with a good resolution index for low intensity stainings. No performance comparisons among instrument brands and models were made. The lyophilized lymphocyte analysis showed an overall frequency of outliers ranging from 3.2% to 19.7%, with a maximum for CD2 FITC (19.7%) and CD3 + HLA-DR + (12.1%). A strongly negative relationship was evident between the FITC threshold and the number of CD2+ cells, whereas the sensitivity threshold had virtually no effects on the measured level of higher antigen density markers like CD4 and many others. Absolute fluorescence intensity measurements of CD4+ and CD19+ were also made. This study design proved valid and suitable for a large-scale evaluation of both instrument performance and cytometer operators' skill. A number of practical problems were identified among participants, thus stressing the need for more effective educational programmes and technical guidelines.

摘要

意大利细胞计量学会(Gruppo Italiano di Citometria,GIC)于1991年发起了这项关于细胞免疫表型分析和流式细胞仪性能的全国性大规模质量控制试验。这项独立研究的目的是使用校准荧光微珠评估仪器性能(FITC的最低阈值、线性、荧光变异系数和分辨率指标),并将其与使用多种抗体对冻干淋巴细胞表面免疫荧光染色的测量结果相关联(阳性细胞百分比和荧光平均强度)。向意大利各地拥有350台仪器的306个实验室进行了一次统一发放。每个试剂盒都包含匿名小瓶,其中装有预混合的校准微珠、冻干的人类淋巴细胞和少量偶联单克隆抗体,用于单FITC和双FITC/PE染色。还要求参与者使用他们自己的抗CD4单克隆抗体。209个实验室使用221台仪器返回了有效答案。设门不是一个检测变量。FITC的最低灵敏度阈值范围为26.6至11,293 MESF,就FITC阈值与荧光变异系数之间的关系而言,仪器存在明显的异质性。低FITC阈值也与低强度染色的良好分辨率指标相关。未对仪器品牌和型号进行性能比较。冻干淋巴细胞分析显示异常值的总体频率范围为3.2%至19.7%,其中CD2 FITC(19.7%)和CD3 + HLA-DR +(12.1%)的异常值最多。FITC阈值与CD2 +细胞数量之间存在明显的负相关关系,而灵敏度阈值对CD4等较高抗原密度标志物以及许多其他标志物的测量水平几乎没有影响。还对CD4 +和CD19 +进行了绝对荧光强度测量。该研究设计被证明是有效的,适用于对仪器性能和流式细胞仪操作人员技能的大规模评估。在参与者中发现了一些实际问题,从而强调了更有效的教育计划和技术指南的必要性。

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