Immune reconstitution following allogeneic peripheral blood progenitor cell transplantation:: Comparison of recipients of positive CD34+ selected grafts with recipients of unmanipulated grafts

被引:78
作者
Martínez, C [1 ]
Urbano-Ispizua, A [1 ]
Rozman, C [1 ]
Marín, P [1 ]
Rovira, M [1 ]
Sierra, J [1 ]
Montfort, N [1 ]
Carreras, E [1 ]
Montserrat, E [1 ]
机构
[1] Univ Barcelona, Hosp Clin,Hematol Dept, Inst Invest Biomed August Pi & Sunyer, Postgrad Sch Hematol Farreras Valenti, E-08036 Barcelona, Spain
关键词
immune reconstitution; peripheral blood progenitor cells; allogeneic transplantation;
D O I
10.1016/S0301-472X(98)00029-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We compared the kinetic recovery of lymphocytes and their subsets in two groups of patients submitted to allogeneic peripheral blood progenitor cell transplantation (allo-PBT): those receiving lymphocyte-depleted leukaphereses by positive selection of CD34(+) cells (group 1, n = 18) and those receiving unmanipulated leukaphereses (group 2, n = 15). Patients were conditioned with cyclophosphamide (120 mg/kg) and fractioned total body irradiation (13 Gy, group 1; 12 Gy, group 2). The mean number (x10(6)/kg) of CD34(+) and CD3(+) cells infused was 4.0 and 0.67, respectively, in group 1 patients, and 4.7 and 274, respectively, for group 2 patients. Graft-versus-host disease prophylaxis consisted of cyclosporin A + methylprednisolone for group I and cyclosporin A + methotrexate for group 2. Median follow-up was 7 months (range 2-8 months) for both groups. During the first 6 months post-transplant, CD4(+) cell counts were lower in group 1 as compared with group 2 (p = 0.014, 0.010, 0.011, 0.0003, and 0.052 at 0.5, 1, 2, 3, and 6 months, respectively), whereas there was no difference at 8 months. The number of CD4(+)CD45RA(+) cells was very low throughout the study in both groups, being lower in group 1 than in group 2, especially during the first 3 months posttransplant (p = 0.007 and 0.0006 at 1 and 3 months). Normal levels of CD8(+) cells were reached by 1 month post-transplant in both groups. TCR gamma delta(+) cell counts were lower in group 1 than in group 2 during the first 4 months post-transplant (p = 0.001, 0.004, and 0.04 at 1, 3, and 4 months). A normal number of natural killer cells (CD3(-)CD56(+)) was achieved 1 month posttransplant in both groups. B lymphocytes (CD19(+)) showed low or undetectable counts throughout the first 4 months in both groups, achieving the normal range at 8 months. These results show that, during the first 6 months-following allo-PBT with CD34(+) selected grafts, the number of CD4(+), CD4(+)CD45RA(+), and TCR gamma delta(+) cells is significantly lower than after unmanipulated allo-PBT; these differences disappeared at 8 months. In contrast, there are no differences between transplant groups in the recovery of CD8(+), CD19(+), and natural killer cells. (C) 1999 International Society for Experimental Hematology. Published by Elsevier Science Inc.
引用
收藏
页码:561 / 568
页数:8
相关论文
共 53 条
[1]   A COMPUTER-MODEL OF UTERINE CONTRACTIONS BASED ON DISCRETE CONTRACTILE ELEMENTS [J].
ANDERSEN, HF ;
BARCLAY, ML .
OBSTETRICS AND GYNECOLOGY, 1995, 86 (01) :108-111
[2]  
APPELBAUM FR, 1989, NEW DIRECTIONS CANC, P1
[3]  
ATKINSON K, 1990, BONE MARROW TRANSPL, V5, P209
[4]   TRANSPLANTATION OF ALLOGENEIC PERIPHERAL-BLOOD STEM-CELLS MOBILIZED BY RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR [J].
BENSINGER, WI ;
WEAVER, CH ;
APPELBAUM, FR ;
ROWLEY, S ;
DEMIRER, T ;
SANDERS, J ;
STORB, R ;
BUCKNER, CD .
BLOOD, 1995, 85 (06) :1655-1658
[5]   Lethal murine graft-versus-host disease induced by donor gamma/delta expressing T cells with specificity for host nonclassical major histocompatibility complex class Ib antigens [J].
Blazar, BR ;
Taylor, PA ;
PanoskaltsisMortari, A ;
Barrett, TA ;
Bluestone, JA ;
Vallera, DA .
BLOOD, 1996, 87 (02) :827-837
[6]   Murine gamma/delta-expressing T cells affect alloengraftment via the recognition of nonclassical major histocompatibility complex class Ib antigens [J].
Blazar, BR ;
Taylor, PA ;
Bluestone, JA ;
Vallera, DA .
BLOOD, 1996, 87 (10) :4463-4472
[7]  
BRIDGE J, 1990, BONE MARROW TRANS S2, V5, P111
[8]   Study of hematopoietic chimerism following allogeneic peripheral blood stem cell transplantation using PCR amplification of short tandem repeats [J].
Briones, J ;
UrbanoIspizua, A ;
Rozman, C ;
Marin, P ;
Carreras, E ;
Rovira, M ;
Sierra, J ;
Colomer, D ;
Martinez, C ;
Montserrat, E .
ANNALS OF HEMATOLOGY, 1996, 72 (04) :265-268
[9]  
Craston Rose, 1997, British Journal of Haematology, V97, P40
[10]  
DEGAST GC, 1985, BLOOD, V66, P428