Suppr超能文献

北欧血液及自体移植物中CD34+细胞计数流式细胞术标准的验证:第三届研讨会报告。北欧干细胞实验室小组

Validation of the Nordic flow cytometry standard for CD34+ cell enumeration in blood and autografts: report from the third workshop. Nordic Stem Cell Laboratory Group.

作者信息

Johnsen H E, Baech J, Nikolajsen K

机构信息

The Department of Haematology, Herlev Hospital, University of Copenhagen, Denmark.

出版信息

J Hematother. 1999 Feb;8(1):15-28. doi: 10.1089/106161299320532.

Abstract

Following two workshops on standardization of enumeration of CD34+ cells in blood and leukapheresis products, the Nordic Stem Cell Laboratory Group (NSCL-G) evaluated the Milan/Mulhouse/Nordic standard in clinical practice during the third workshop (WS-III). This report documents an acceptable interlaboratory variation in the most clinically active laboratories, with a coefficient of variation (CV) below 0.19 in 7 of 8 analyses performed. The introduction of a pan-CD45 antibody in the analysis did not improve the CV. Comparison of two different CD34 class II antibodies on a total of 99 samples and procedures with and without washing on a total of 96 samples revealed a significant correlation (r2 >0.99) for all analyses. Finally, subset analysis of uncommitted and lineage-specific progenitors revealed major gating difficulties, indicating that further improvements are necessary. In an analysis of more than 600 patients undergoing mobilization and harvest of blood progenitors, with about 500 patients autografted, we found a significant correlation between blood levels of CD34+ cells and recovery of CD34+ cells from each harvest as well as between CD34+ cell number reinfused and time to neutrophil and platelet recovery. This report documents for the first time that the very simple Milan/Mulhouse method (termed The Nordic Standard) can be used by a group of laboratories to obtain important clinical information. Consequently, we consider this method as the conventional method in quality assessment of autografts, which should provide a benchmark for development of second-generation improvements.

摘要

在举办了两次关于血液和白细胞分离产品中CD34+细胞计数标准化的研讨会之后,北欧干细胞实验室小组(NSCL-G)在第三次研讨会(WS-III)期间评估了米兰/米卢斯/北欧标准在临床实践中的应用情况。本报告记录了在临床最活跃的实验室中可接受的实验室间差异,在进行的8次分析中有7次变异系数(CV)低于0.19。在分析中引入全CD45抗体并未改善CV。对总共99个样本使用两种不同的CD34 II类抗体进行比较,并对总共96个样本进行有无洗涤的程序分析,结果显示所有分析均具有显著相关性(r2>0.99)。最后,对未定向和谱系特异性祖细胞的亚群分析显示出主要的设门困难,表明有必要进一步改进。在对600多名接受血液祖细胞动员和采集的患者进行分析时,其中约500名患者接受了自体移植,我们发现血液中CD34+细胞水平与每次采集的CD34+细胞回收率之间以及回输的CD34+细胞数量与中性粒细胞和血小板恢复时间之间存在显著相关性。本报告首次记录了一组实验室可以使用非常简单的米兰/米卢斯方法(称为北欧标准)来获取重要的临床信息。因此,我们认为该方法是自体移植质量评估中的传统方法,应为第二代改进方法的开发提供基准。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验