Natural killer cell activity influences outcome after T cell depleted stem cell transplantation from matched unrelated and haploidentical donors

被引:20
|
作者
Lang, Peter [1 ]
Pfeiffer, Matthias [1 ]
Teltschik, Heiko-Manuel [1 ]
Schlegel, Patrick [1 ]
Feuchtinger, Tobias [1 ]
Ebinger, Martin [1 ]
Klingebiel, Thomas [2 ]
Bader, Peter [2 ]
Schlegel, Paul-Gerhard [3 ]
Beck, James [4 ]
Greil, Johann [5 ]
Handgretinger, Rupert [1 ]
机构
[1] Univ Tubingen, Dept Pediat Hematol & Oncol, Univ Childrens Hosp Tuebingen, Tubingen, Germany
[2] Goethe Univ Frankfurt, Dept Pediat Hematol & Oncol, Univ Childrens Hosp Frankfurt, D-6000 Frankfurt, Germany
[3] Univ Wurzburg, Dept Pediat Oncol, Univ Childrens Hosp Wuerzburg, Wurzburg, Germany
[4] Univ Jena, Dept Hematol & Oncol, Univ Childrens Hosp Jena, D-6900 Jena, Germany
[5] Univ Heidelberg, Dept Hematol & Oncol, Univ Childrens Hosp Heidelberg, D-6900 Heidelberg, Germany
关键词
haploidentical; transplantation; natural killer; relapse; leukemia; BONE-MARROW-TRANSPLANTATION; RISK ACUTE-LEUKEMIA; CLASS-I EXPRESSION; PERIPHERAL-BLOOD; PEDIATRIC-PATIENTS; NK CELLS; CHILDREN; RELAPSE; BLASTS; RECEPTORS;
D O I
10.1016/j.beha.2011.04.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lytic activity and recovery of natural killer (NK) cells was monitored in pediatric patients with leukemias (ALL, AML, CML, JMML) and myelodysplastic syndromes after transplantation of T cell depleted stem cells from matched unrelated (n = 18) and mismatched related (haploidentical, n = 29) donors. CD34 + selection with magnetic microbeads resulted in 8 x 10(3)/kg residual T cells. No post-transplant immune suppression was given. NK cells recovered rapidly after transplantation (300 CD56+/mu L at day 30, median), whereas T cell recovery was delayed (median: 12 CD3+/mu L at day 90). NK activity was measured as specific lysis of K 562 targets several times (mean: 3 assays per patient). Four temporal patterns of lyric activity could be differentiated: consistently low, consistently high, decreasing and increasing activity. Patients with consistently high or increasing activity had significantly lower relapse probability than patients with consistently low or decreasing levels (0.18 vs 0.73 at 2 years, p < 0.05). The subgroup of patients with ALL showed similar results (0.75 vs 0.14 at 2 years, p < 0.05). Speed of T cell recovery had no influence. These data suggest that both achieving and maintaining a high level of NK activity may contribute to prevent relapse. Since NK activity could be markedly increased by in vitro stimulation with Interleukin 2 (IL-2), in vivo administration should be considered. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:403 / 411
页数:9
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