Impact of cryopreservation on B cell chronic lymphocytic leukaemia phenotype

被引:15
作者
Deneys, V [1 ]
Thiry, V [1 ]
Hougardy, N [1 ]
Mazzon, AM [1 ]
Leveugle, P [1 ]
De Bruyère, M [1 ]
机构
[1] Univ Catholique Louvain, Univ Hosp, Immunohaematol Lab, B-1200 Brussels, Belgium
关键词
chronic lymphocytic leukaemia; immunophenotype; cryopreservation; flow cytometry; cluster of differentiation;
D O I
10.1016/S0022-1759(99)00089-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background and objectives: Freezing is a practical approach for cell preservation for retrospective studies. The aim of this work was to check the cryopreservation impact on B cell chronic lymphocytic leukaemia phenotype. Material and methods: Blood samples from 15 CLL patients were analyzed freshly and after freezing at -196 degrees C, without separation, and thawing. Results were compared by Student's paired t-test. Results: The phenotype of fresh CLL cells was as follows: CD19 +, CD5 +, faint CD20, CD23 +/-, weak CD22 and sig, CD37 +, HLA-DR +, FMC7 -. After cryopreservation, the percentage of CD5 and CD23 positive cells decreased, whereas HLA-DR positive cells increased moderately. The CLL Matures's score was modified in 6 cases out of 15 (40%). Conclusion: Cryopreservation modifies B cell chronic lymphocytic leukaemia phenotype, by decreasing CD5 and CD23 expression. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 21 条
[1]  
[Anonymous], ATLAS LYMPHOID HYPER
[2]  
BARCLAY AN, 1997, LEUCOCYTE ANTIGEN
[3]   Evaluation of methods for preparing and thawing cryopreserved CD34+ and CD34- cell lines for use as reagents in flow cytometry of hematopoietic progenitor cells [J].
Bowman, CA ;
Yu, M ;
CottlerFox, M .
TRANSFUSION, 1996, 36 (11-12) :985-988
[4]   EXPRESSION OF IMMUNOLOGICAL MARKERS ON LEUKEMIC-CELLS BEFORE AND AFTER CRYOPRESERVATION AND THAWING [J].
CAMPOS, L ;
GUYOTAT, D ;
LARESE, A ;
ARCHIMBAUD, E ;
MAZET, L ;
EHRSAM, A ;
FIERE, D .
CRYOBIOLOGY, 1988, 25 (01) :18-22
[5]  
Fiebig EW, 1997, CYTOMETRY, V29, P340, DOI 10.1002/(SICI)1097-0320(19971201)29:4<340::AID-CYTO11>3.0.CO
[6]  
2-U
[7]   QUALITY-CONTROL IN CLINICAL FLOW-CYTOMETRY [J].
HARVATH, L .
PATHOLOGY AND IMMUNOPATHOLOGY RESEARCH, 1988, 7 (05) :338-344
[8]   PERIPHERAL-BLOOD CELL PREPARATION INFLUENCES THE LEVEL OF EXPRESSION OF LEUKOCYTE CELL-SURFACE MARKERS AS ASSESSED WITH QUANTITATIVE MULTICOLOR FLOW-CYTOMETRY [J].
ISLAM, D ;
LINDBERG, AA ;
CHRISTENSSON, B .
CYTOMETRY, 1995, 22 (02) :128-134
[9]  
KAROW A M JR, 1965, Cryobiology, V2, P99, DOI 10.1016/S0011-2240(65)80094-3
[10]  
Keeney M, 1998, CYTOMETRY, V34, P280, DOI 10.1002/(SICI)1097-0320(19981215)34:6<280::AID-CYTO6>3.0.CO