Quality assurance of stem cell enumeration by flow cytometry

被引:0
|
作者
Chin-Yee, I
Anderson, L
Keeney, M
Sutherland, DR
机构
[1] Univ Western Ontario, London Hth Sci Ctr, London, ON N6A 4G5, Canada
[2] Toronto Hosp, Toronto, ON M5T 2S8, Canada
[3] NE Ontario Reg Canc Ctr, Sudbury, ON, Canada
[4] Canadian Red Cross Blood Transfus Serv, Ottawa Ctr, Ottawa, ON, Canada
[5] Hop Maison Neuve Rosemont, Div Hematol, Montreal, PQ, Canada
[6] Hop St Sacrement, Quebec City, PQ, Canada
[7] Univ Alberta Hosp, Dept Lab Med, Edmonton, AB T6G 2B7, Canada
[8] Hosp Sick Children, Haematol Lab, Toronto, ON M5G 1X8, Canada
[9] Foothills Hosp, Calgary, AB T2N 2T9, Canada
[10] Hotel Dieu, Lab Cytometrie, Montreal, PQ, Canada
[11] Hamilton Gen Hosp, Dept Lab Med, Hamilton, New Zealand
[12] Hop Sacre Coeur, Serv Hematol Oncol, Montreal, PQ H4J 1C5, Canada
[13] Sunnybrook Hlth Sci Ctr, Toronto, ON M4N 3M5, Canada
[14] Hop Gen Juif Sir Mortimer B Davis, Special Hematol Lab, Montreal, PQ, Canada
[15] British Columbia Childrens Hosp, Immunol Lab, Vancouver, BC V6H 3V4, Canada
[16] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[17] Victoria Gen Hosp, Div Hematol, Halifax, NS B3H 2Y9, Canada
来源
CYTOMETRY | 1997年 / 30卷 / 06期
关键词
quality assurance; CD34; hematopoietic stem cells; standardization;
D O I
10.1002/(SICI)1097-0320(19971215)30:6<296::AID-CYTO5>3.0.CO;2-E
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The enumeration of CD34+ cells by flow cytometry is commonly employed to assess progenitor/stem cell numbers in peripheral blood, cord blood, and apheresis products used for peripheral blood stem cell transplantation (PBSCT). Until recently, the enumeration of CD34+ cells has evolved in the absence of any procedural guidelines or quality assurance programs. We established a voluntary quality assurance for stem cell enumeration (QASE) program for Canadian laboratories involved in PBSCT. The goals of this study were 1) to survey current flow cytometric procedures for CD34 enumeration; 2) to evaluate inter-institutional reproducibility of currently employed assays; and 3) to evaluate the impact of adoption of a common method on inter-laboratory variability. Fourteen to nineteen laboratories participated in this program by enumerating CD34+ cells in shared cord blood samples. The survey showed a wide variation in flow cytometric methodology which in part contributed to the wide range in results obtained between different centres. Major differences in methodology included the number of events counted, use of isotype control and gating strategy. Participation in this program and adoption of a common methodology increased level of agreement for any given result although this trend did not reach statistical significance (P = 0.13). The results of this survey emphasize the need for a quality assurance program for stem cell enumeration by flow cytometry. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:296 / 303
页数:8
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