Whole-blood leukoreduction filters are a source for cryopreserved cells for phenotypic and functional investigations on peripheral blood lymphocytes

被引:27
|
作者
Néron, S
Dussault, N
Racine, C
机构
[1] Hema Quebec, Res & Dev, Cellular Engn, Ste Foy, PQ G1V 5C3, Canada
[2] Univ Laval, Dept Biochem & Microbiol, Ste Foy, PQ G1K 7P4, Canada
关键词
D O I
10.1111/j.1537-2995.2006.00772.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Leukoreduction of blood is now widely performed by blood banks, and the possibility of recovering 10(8) to 10(9) white blood cells (WBCs) from leukoreduction filters, which are usually discarded, represents a promising source for normal human cells. Previous studies with these filters to prepare WBCs have performed their experimentation with fresh cells only. Whether these filter-derived cells could also be used to prepare frozen cell banks to facilitate work organization and open new avenues for their utilization as references in physiological studies and clinical investigations was investigated. STUDY DESIGN AND METHODS: Blood samples or whole-blood leukoreduction filters were obtained, after informed consent, from volunteers or blood donors, respectively. The proportions of CD3+, CD14+, CD16+, CD19+, and CD45+ cells within peripheral blood mononuclear cells (PBMNCs) were determined by flow cytometry from all samples. B cells were isolated and their functional responses were evaluated in vitro. RESULTS: The yield of PBMNCs recovered from whole-blood leukoreduction filters was lower (50%) than the one with fresh blood samples but still provided 2 x 10(8) to 4 x 10(8) PBMNCs per unit. After one cycle of freezing-thawing, the proportions of B- and T-cell populations were similar to normal blood values. Purified B cells issued from whole-blood leukoreduction filters displayed normal phenotypes and functions. CONCLUSION: Leukoreduction filters represent a valuable source of PBMNCs. These cells could be easily recovered to prepare frozen cell banks useful in basic phenotypic and functional analyses involving the main subsets of B cells and the global T-cell population.
引用
收藏
页码:537 / 544
页数:8
相关论文
共 50 条
  • [41] PHENOTYPIC AND FUNCTIONAL-ANALYSIS OF PERIPHERAL-BLOOD LYMPHOCYTES IN ORAL LICHEN-PLANUS
    SUGERMAN, PB
    VOLTZ, MJ
    SAVAGE, NW
    BASFORD, KE
    SEYMOUR, GJ
    JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1992, 21 (10) : 445 - 450
  • [42] Phenotypic profile of peripheral blood lymphocytes from European bovines
    Bittar, JFF
    Ribeiro, MFB
    Marciano, APV
    Salcedo, JHP
    Martins-Filho, OA
    ARQUIVO BRASILEIRO DE MEDICINA VETERINARIA E ZOOTECNIA, 2004, 56 (01) : 107 - 110
  • [43] NEONATAL AND MATERNAL LYMPHOCYTES IN WHOLE-BLOOD CULTURES - ABSENCE OF STRONG INTERACTION
    EIBERG, H
    MOHR, J
    NIELSEN, KR
    VOX SANGUINIS, 1978, 35 (05) : 288 - 293
  • [44] A RAPID MICROTECHNIQUE FOR INVITRO STIMULATION OF CANINE LYMPHOCYTES USING WHOLE-BLOOD
    FELSBURG, PJ
    REILLEY, MT
    SINNIGEN, JK
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1980, 1 (03) : 251 - 261
  • [45] PHENOTYPIC ANALYSIS OF PERIPHERAL-BLOOD LYMPHOCYTES AND INTESTINAL INTRAEPITHELIAL LYMPHOCYTES IN CALVES
    WATERS, WR
    HARP, JA
    NONNECKE, BJ
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1995, 48 (3-4) : 249 - 259
  • [46] ISOLATION OF OVINE LYMPHOCYTES AND GRANULOCYTES FROM WHOLE-BLOOD USING HYDROXYETHYLCELLULOSE
    KERRY, PJ
    RESEARCH IN VETERINARY SCIENCE, 1976, 21 (03) : 356 - 357
  • [47] Phenotypic and Functional Plasticity of CXCR6+ Peripheral Blood NK Cells
    Angelo, Laura S.
    Hogg, Graham D.
    Abeynaike, Shawn
    Bimler, Lynn
    Vargas-Hernandez, Alexander
    Paust, Silke
    FRONTIERS IN IMMUNOLOGY, 2022, 12
  • [48] MEASUREMENT OF HUMAN-ENDOTHELIAL CELLS IN WHOLE-BLOOD
    TAKAHASHI, H
    HARKER, LA
    THROMBOSIS RESEARCH, 1983, 31 (01) : 1 - 12
  • [49] WHOLE-BLOOD VERSUS PACKED RED-CELLS
    HEAD, DR
    TRANSFUSION, 1985, 25 (06) : 591 - 591
  • [50] FLOW CYTOMETRIC ANALYSIS OF DENDRITIC CELLS IN WHOLE-BLOOD
    MACEY, MG
    MCCARTHY, DA
    BROWNK, A
    KNIGHT, SC
    NEWLAND, AC
    PATHOLOGIE BIOLOGIE, 1994, 42 (08): : 807 - 807