ClearLLab 10C reagents panel can be applied to analyze paucicellular samples by flow cytometry.

IF 2.3 3区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY Cytometry Part B: Clinical Cytometry Pub Date : 2024-11-18 DOI:10.1002/cyto.b.22215
Małgorzata Kajstura, Tia LaBarge, Andrew G Evans
{"title":"ClearLLab 10C reagents panel can be applied to analyze paucicellular samples by flow cytometry.","authors":"Małgorzata Kajstura, Tia LaBarge, Andrew G Evans","doi":"10.1002/cyto.b.22215","DOIUrl":null,"url":null,"abstract":"<p><p>The FDA-approved ClearLLab 10C Reagents Panel (Beckman Coulter) simplified the diagnosis of leukemias and lymphomas by flow cytometry. However, the requirement of using 3 × 10<sup>6</sup> cells/mL cannot be met for paucicellular samples. Therefore, we tested whether this 10-color panel can be reliably employed to analyze specimens with low cell concentrations. Serial dilutions of 16 samples (5 normal, 11 abnormal), yielding concentrations ranging from 3.0 × 10<sup>6</sup> to 0.0469 × 10<sup>6</sup> cells/mL (64-fold difference), were stained using the B-cell and T-cell panels of the ClearLLab 10C system, and mean fluorescence intensity (MFI) was measured for each antibody. For each cell dilution, the deviation from the value obtained with the FDA-approved concentration of 3.0 × 10<sup>6</sup> cells/mL was calculated. The agreement between the highest and lowest cell concentration data was evaluated by the Bland and Altman method, Pearson's and Spearman's correlation analyses, and linear regression. In all patients, the antigen expression pattern was similar at all cell concentrations tested, and the mean deviation of the MFI from the value obtained using 3.0 × 10<sup>6</sup> cells/mL never exceeded 10% for any of the antibodies. The Bland-Altman method demonstrated the similarity between results obtained with the FDA-approved cell concentration and a 64-fold diluted cell suspension, and a high positive correlation was found between MFI acquired under these two conditions. The tests utilizing the lowest density of cells yielded the same patterns of antigen expression in all patients as those performed with the FDA-approved concentration, documenting a 100% concordance between these two protocols. The ClearLLab 10C panel can reliably determine the expression of markers of leukemias and lymphomas in paucicellular samples containing as little as 0.0469 × 10<sup>6</sup> cells/mL (64-fold lower than the FDA-approved concentration). This finding markedly expands the applicability of the ClearLLab 10C platform in a clinical setting.</p>","PeriodicalId":10883,"journal":{"name":"Cytometry Part B: Clinical Cytometry","volume":" ","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytometry Part B: Clinical Cytometry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/cyto.b.22215","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The FDA-approved ClearLLab 10C Reagents Panel (Beckman Coulter) simplified the diagnosis of leukemias and lymphomas by flow cytometry. However, the requirement of using 3 × 106 cells/mL cannot be met for paucicellular samples. Therefore, we tested whether this 10-color panel can be reliably employed to analyze specimens with low cell concentrations. Serial dilutions of 16 samples (5 normal, 11 abnormal), yielding concentrations ranging from 3.0 × 106 to 0.0469 × 106 cells/mL (64-fold difference), were stained using the B-cell and T-cell panels of the ClearLLab 10C system, and mean fluorescence intensity (MFI) was measured for each antibody. For each cell dilution, the deviation from the value obtained with the FDA-approved concentration of 3.0 × 106 cells/mL was calculated. The agreement between the highest and lowest cell concentration data was evaluated by the Bland and Altman method, Pearson's and Spearman's correlation analyses, and linear regression. In all patients, the antigen expression pattern was similar at all cell concentrations tested, and the mean deviation of the MFI from the value obtained using 3.0 × 106 cells/mL never exceeded 10% for any of the antibodies. The Bland-Altman method demonstrated the similarity between results obtained with the FDA-approved cell concentration and a 64-fold diluted cell suspension, and a high positive correlation was found between MFI acquired under these two conditions. The tests utilizing the lowest density of cells yielded the same patterns of antigen expression in all patients as those performed with the FDA-approved concentration, documenting a 100% concordance between these two protocols. The ClearLLab 10C panel can reliably determine the expression of markers of leukemias and lymphomas in paucicellular samples containing as little as 0.0469 × 106 cells/mL (64-fold lower than the FDA-approved concentration). This finding markedly expands the applicability of the ClearLLab 10C platform in a clinical setting.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ClearLLab 10C 试剂盒可用于流式细胞仪分析白细胞样本。
美国食品和药物管理局批准的 ClearLLab 10C 试剂盒(Beckman Coulter)简化了流式细胞术对白血病和淋巴瘤的诊断。然而,对于白细胞样本,使用 3 × 106 cells/mL 的要求无法满足。因此,我们测试了这种 10 色板能否可靠地用于分析细胞浓度较低的样本。使用 ClearLLab 10C 系统的 B 细胞和 T 细胞面板对 16 份样本(5 份正常,11 份异常)进行连续稀释,得到的细胞浓度范围为 3.0 × 106 到 0.0469 × 106 cells/mL(相差 64 倍),然后测量每种抗体的平均荧光强度 (MFI)。对于每个细胞稀释度,计算与美国食品药品管理局批准的 3.0 × 106 cells/mL 浓度值的偏差。最高和最低细胞浓度数据之间的一致性通过布兰德和阿尔特曼法、皮尔逊和斯皮尔曼相关分析以及线性回归进行评估。所有患者的抗原表达模式在测试的所有细胞浓度下都相似,任何抗体的 MFI 与使用 3.0 × 106 cells/mL 所获数值的平均偏差从未超过 10%。Bland-Altman 方法表明,使用 FDA 批准的细胞浓度和稀释 64 倍的细胞悬浮液得到的结果具有相似性,而且在这两种条件下得到的 MFI 之间具有高度的正相关性。使用最低细胞密度进行的检测在所有患者中得出的抗原表达模式与使用 FDA 批准浓度进行的检测结果相同,这两种方案的一致性达到了 100%。ClearLLab 10C 检测试剂盒能可靠地检测白血病和淋巴瘤标志物在细胞密度低至 0.0469 × 106 cells/mL 的白细胞样本中的表达(比 FDA 批准的浓度低 64 倍)。这一发现大大扩展了 ClearLLab 10C 平台在临床环境中的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.80
自引率
32.40%
发文量
51
审稿时长
>12 weeks
期刊介绍: Cytometry Part B: Clinical Cytometry features original research reports, in-depth reviews and special issues that directly relate to and palpably impact clinical flow, mass and image-based cytometry. These may include clinical and translational investigations important in the diagnostic, prognostic and therapeutic management of patients. Thus, we welcome research papers from various disciplines related [but not limited to] hematopathologists, hematologists, immunologists and cell biologists with clinically relevant and innovative studies investigating individual-cell analytics and/or separations. In addition to the types of papers indicated above, we also welcome Letters to the Editor, describing case reports or important medical or technical topics relevant to our readership without the length and depth of a full original report.
期刊最新文献
Prospective feasibility of a minimal BH3 profiling assay in acute myeloid leukemia. PICALM::MLLT10 fusion gene positive acute myeloid leukemia with PHF6 mutation and presented with CD7 positive immunophenotype. SingletSeeker: an unsupervised clustering approach for automated singlet discrimination in cytometry. ClearLLab 10C reagents panel can be applied to analyze paucicellular samples by flow cytometry. Improved identification of clinically relevant Acute Leukemia subtypes using standardized EuroFlow panels versus non-standardized approach.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1