Real-time quantitative y chromosome-specific PCR (QYCS-PCR) for monitoring hematopoietic chimerism after sex-mismatched allogeneic stem cell transplantation

被引:67
作者
Fehse, B
Chukhlovin, A
Kühlcke, K
Marinetz, O
Vorwig, O
Renges, H
Krüger, W
Zabelina, T
Dudina, O
Finckenstein, FG
Kröger, N
Kabisch, H
Hochhaus, A
Zander, AR
机构
[1] Univ Hamburg, Hosp Eppendorf, Bone Marrow Transplantat Ctr, D-20251 Hamburg, Germany
[2] Pavlov State Med Univ St Petersburg, St Petersburg, Russia
[3] EUFETS, Idar Oberstein, Germany
[4] Univ Hamburg, Hosp Eppendorf, Dept Pediat Hematol Oncol, D-20251 Hamburg, Germany
[5] Univ Hosp Mannheim, Mannheim, Germany
来源
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH | 2001年 / 10卷 / 03期
关键词
D O I
10.1089/152581601750289028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Y chromosome-specific sequences can be used to detect remaining male cells after sex-mismatched allogeneic blood stem cell transplantation (HSCT) involving a male patient and female donor, which represents approximately 25% of all cases. We developed a quantitative Y chromosome-specific PCR assay (QYCS-PCR) based on the DFFRY gene for the determination of hematopoietic donor chimerism. We analyzed blood and marrow samples from more than 40 patients at various time points after both standard and nonmyeloablative allogeneic HSCT. We found that real-time PCR combines extreme sensitivity, with a detection level of less than 1 male in 100,000 female cells (<0.001%), with very good reproducibility, especially in the important range of minor host chimerism. QYCS-PCR results were in close agreement with data from other techniques as bcr/abl-PCR and/or fluorescent in situ hybridization (FISH) analysis. In two relapsed patients, increasing numbers of Y-positive hematopoietic cells indicated recurrence of malignant disease prior to clinical confirmation. In conclusion, quantitative Y chromosome-specific PCR is a promising approach for monitoring the extent of chimerism in blood and other tissues after sex-mismatched hematopoietic stem cell transplantation (HSCT) or organ transplantation.
引用
收藏
页码:419 / 425
页数:7
相关论文
共 16 条
  • [1] Mixed hematopoietic chimerism after allogeneic bone marrow transplantation: The impact of quantitative PCR analysis for prediction of relapse and graft rejection in children
    Bader, P
    Holle, W
    Klingebiel, T
    Handgretinger, R
    Benda, N
    Schlegel, PG
    Niethammer, D
    Beck, J
    [J]. BONE MARROW TRANSPLANTATION, 1997, 19 (07) : 697 - 702
  • [2] Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and manning to the Sxrb interval of the mouse Y chromosome of the Dffry gene
    Brown, GM
    Furlong, RA
    Sargent, CA
    Erickson, RP
    Longepied, G
    Mitchell, M
    Jones, MH
    Hargreave, TB
    Cooke, HJ
    Affara, NA
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (01) : 97 - 107
  • [3] Accurate and rapid analysis of residual disease in patients with CML using specific fluorescent hybridization probes for real time quantitative RT-PCR
    Emig, M
    Saussele, S
    Wittor, H
    Weisser, A
    Reiter, A
    Willer, A
    Berger, U
    Hehlmann, R
    Cross, NCP
    Hochhaus, A
    [J]. LEUKEMIA, 1999, 13 (11) : 1825 - 1832
  • [4] Efficient depletion of alloreactive donor T lymphocytes based on expression of two activation-induced antigens (CD25 and CD69)
    Fehse, B
    Frerk, O
    Goldmann, M
    Bulduk, M
    Zander, AR
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2000, 109 (03) : 644 - 651
  • [5] Persistent donor chimaerism is consistent with disease-free survival following BMT for chronic myeloid leukaemia
    Gardiner, N
    Lawler, M
    ORiordan, J
    DeArce, M
    Humphries, P
    McCann, SR
    [J]. BONE MARROW TRANSPLANTATION, 1997, 20 (03) : 235 - 241
  • [6] Engraftment of allogeneic hematopoietic progenitor cells with purine analog-containing chemotherapy: Harnessing graft-versus-leukemia without myeloablative therapy
    Giralt, S
    Estey, E
    Albitar, M
    vanBesien, K
    Rondon, G
    Anderlini, P
    OBrien, S
    Khouri, I
    Gajewski, J
    Mehra, R
    Claxton, D
    Andersson, B
    Beran, M
    Przepiorka, D
    Koller, C
    Kornblau, S
    Korbling, M
    Keating, M
    Kantarjian, H
    Champlin, R
    [J]. BLOOD, 1997, 89 (12) : 4531 - 4536
  • [7] HILL RS, 1986, BLOOD, V67, P811
  • [8] DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE
    HOLLAND, PM
    ABRAMSON, RD
    WATSON, R
    GELFAND, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7276 - 7280
  • [9] Huss R, 1996, BONE MARROW TRANSPL, V18, P767
  • [10] Accurate estimation of transduction efficiency necessitates a multiplex real-time PCR
    Klein, D
    Bugl, B
    Günzburg, WH
    Salmons, B
    [J]. GENE THERAPY, 2000, 7 (06) : 458 - 463