• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

一种用于检测和计数血小板及单核细胞制品中低水平残留红细胞的流式细胞术方法。

A flow cytometric method for detection and enumeration of low-level, residual red blood cells in platelets and mononuclear cell products.

作者信息

Santana Julie M, Dumont Larry J

机构信息

R&D, Gambro BCT, Inc., Lakewood, Colorado 80215, USA.

出版信息

Transfusion. 2006 Jun;46(6):966-72. doi: 10.1111/j.1537-2995.2006.00829.x.

DOI:10.1111/j.1537-2995.2006.00829.x
PMID:16734813
Abstract

BACKGROUND

Conventional automated cell counters cannot accurately count residual red blood cells (rRBCs) that are often present in various blood products. A two-color flow cytometric method (FC) was validated for detecting and enumerating rRBCs in platelets (PLTs) and mononuclear cell (MNC) products.

STUDY DESIGN AND METHODS

PLT and MNC products for PLTs (CD61-fluorescein isothiocyanate) and rRBC (anti-glycophorin A-phycoerythrin) were double stained, and data were acquired with a flow cytometer. Assay linearity, accuracy, and precision were assessed with a standard-dilution series of rRBCs. This assay was used to determine the rRBCs of apheresis PLTs collected with Trima Accel (Gambro BCT) and MNC products collected with the COBE Spectra (Gambro BCT).

RESULTS

The linear range of this assay in PLT and MNC products is 10 to 2000 RBCs per microL (R2=0.994). FC had a mean intraassay coefficient of variation of 11.8 percent at 34 RBCs per microL. A standard clinical hematology analyzer overestimated rRBCs in MNC products by 1.59x10(5)+/-0.7x10(5) RBCs per microL. Apheresis PLTs had a median of 17.4 RBCs per microL, with 99.0 percent containing fewer than 90.0 RBCs per microL.

CONCLUSIONS

This method for determining rRBCs in blood products is accurate and repeatable with a lower limit of detection adequate to assess currently available blood products. FC should be considered for determining rRBCs in MNC products.

摘要

背景

传统的自动细胞计数器无法准确计数各种血液制品中常出现的残余红细胞(rRBC)。一种双色流式细胞术方法(FC)已被验证可用于检测和计数血小板(PLT)及单核细胞(MNC)制品中的rRBC。

研究设计与方法

对用于检测PLT(CD61 - 异硫氰酸荧光素)和rRBC(抗血型糖蛋白A - 藻红蛋白)的PLT和MNC制品进行双重染色,并用流式细胞仪获取数据。通过rRBC的标准稀释系列评估测定的线性、准确性和精密度。该测定法用于确定用Trima Accel(甘布罗BCT公司)采集的单采血小板的rRBC以及用COBE Spectra(甘布罗BCT公司)采集的MNC制品的rRBC。

结果

该测定法在PLT和MNC制品中的线性范围为每微升10至2000个红细胞(R2 = 0.994)。FC在每微升34个红细胞时的平均批内变异系数为11.8%。一台标准临床血液学分析仪将MNC制品中的rRBC高估了每微升1.59×10(5)±0.7×10(5)个红细胞。单采血小板的中位数为每微升17.4个红细胞,99.0%的样本每微升含有的红细胞少于90.0个。

结论

这种测定血液制品中rRBC的方法准确且可重复,检测下限足以评估目前可用的血液制品。在确定MNC制品中的rRBC时应考虑使用FC。

相似文献

1
A flow cytometric method for detection and enumeration of low-level, residual red blood cells in platelets and mononuclear cell products.一种用于检测和计数血小板及单核细胞制品中低水平残留红细胞的流式细胞术方法。
Transfusion. 2006 Jun;46(6):966-72. doi: 10.1111/j.1537-2995.2006.00829.x.
2
Flow cytometric assay for the simultaneous determination of residual white blood cells, red blood cells, and platelets in fresh-frozen plasma: validation and two years' experience.流式细胞术检测新鲜冰冻血浆中残余白细胞、红细胞和血小板:验证及两年经验
Transfusion. 2009 Jun;49(6):1195-204. doi: 10.1111/j.1537-2995.2008.02079.x. Epub 2009 Feb 6.
3
A new one-platform flow cytometric method for residual cell counting in platelet concentrates.一种用于血小板浓缩物中残留细胞计数的新型单平台流式细胞术方法。
Transfusion. 2009 Dec;49(12):2604-11. doi: 10.1111/j.1537-2995.2009.02326.x. Epub 2009 Jul 22.
4
Multicenter evaluation of two flow cytometric methods for counting low levels of white blood cells.两种流式细胞术方法用于计数低水平白细胞的多中心评估
Transfusion. 2004 Sep;44(9):1319-24. doi: 10.1111/j.0041-1132.2004.04040.x.
5
Automated CD14+ monocyte collection with the autoMNC program of the COM.TEC cell separator.使用COM.TEC细胞分离器的autoMNC程序自动采集CD14+单核细胞。
Transfusion. 2007 Dec;47(12):2297-304. doi: 10.1111/j.1537-2995.2007.01471.x. Epub 2007 Aug 30.
6
Improved flow cytometric method to enumerate residual cells: minimal linear detection limits for platelets, erythrocytes, and leukocytes.用于计数残留细胞的改进流式细胞术方法:血小板、红细胞和白细胞的最小线性检测限
Cytometry. 2002 Aug 15;50(4):231-7. doi: 10.1002/cyto.10125.
7
Frequently used plateletpheresis techniques result in variable target yields and platelet recruitment of donors.常用的血小板单采技术会导致不同的目标产量以及供体血小板募集量的差异。
Transfusion. 2005 May;45(5):788-97. doi: 10.1111/j.1537-2995.2005.04353.x.
8
Collection of hyperconcentrated platelets with Trima Accel.使用Trima Accel采集高浓缩血小板。
Vox Sang. 2006 Feb;90(2):92-6. doi: 10.1111/j.1423-0410.2005.00721.x.
9
Mononuclear cell variability and recruitment in non-cytokine-stimulated donors after serial 10-liter leukapheresis procedures.连续进行10升白细胞单采程序后,非细胞因子刺激供体中的单核细胞变异性和募集情况。
Transfusion. 2005 Mar;45(3):445-52. doi: 10.1111/j.1537-2995.2005.04202.x.
10
Paired comparison of Gambro Trima Accel versus Baxter Amicus single-needle plateletpheresis.金宝Trima Accel与百特Amicus单针血小板分离术的配对比较。
Transfusion. 2004 Nov;44(11):1612-20. doi: 10.1111/j.0041-1132.2004.04129.x.

引用本文的文献

1
XN-1000 Hematology Analyzer as an Alternative to Flow Cytometry for Measuring Residual Cells in Blood Components.XN-1000血液分析仪作为流式细胞术的替代方法用于检测血液成分中的残留细胞。
Ann Lab Med. 2025 Jul 1;45(4):437-449. doi: 10.3343/alm.2024.0448. Epub 2025 Feb 12.
2
Residual red cells in blood components: A multisite study of fully automated enumeration using a hematology analyzer.血液成分中的残留红细胞:使用血液分析仪进行全自动计数的多站点研究。
Transfusion. 2021 Feb;61(2):568-578. doi: 10.1111/trf.16196. Epub 2020 Nov 17.
3
Rhesus D Antigenic Determinants on Residual Red Blood Cells in Apheresis and Buffy Coat Platelet Concentrates.
单采血小板和富血小板血浆中残余红细胞上的恒河猴D抗原决定簇
Transfus Med Hemother. 2020 Apr;47(2):129-134. doi: 10.1159/000501106. Epub 2019 Jun 27.
4
Low frequency of anti-D alloimmunization following D+ platelet transfusion: the Anti-D Alloimmunization after D-incompatible Platelet Transfusions (ADAPT) study.D+血小板输注后抗-D 同种免疫的发生率较低:D 不相容血小板输注后抗-D 同种免疫(ADAPT)研究。
Br J Haematol. 2015 Feb;168(4):598-603. doi: 10.1111/bjh.13158. Epub 2014 Oct 4.