Rapid natural killer cell recovery determines outcome after T-cell-depleted HLA-identical stem cell transplantation in patients with myeloid leukemias but not with acute lymphoblastic leukemia

被引:146
作者
Savani, B. N.
Mielke, S.
Adams, S.
Uribe, M.
Rezvani, K.
Yong, A. S. M.
Zeilah, J.
Kurlander, R.
Srinivasan, R.
Childs, R.
Hensel, N.
Barrett, A. J.
机构
[1] NHLBI, Stem Cell Allogene Transplantat Sect, Hematol Branch, NIH, Bethesda, MD 20892 USA
[2] NIH, Ctr Clin, Dept Transfus Med, Bethesda, MD 20892 USA
[3] NIH, Ctr Clin, Dept Lab Med, Bethesda, MD 20892 USA
[4] Natl Canc Inst, Urol Oncol Branch, NIH, Bethesda, MD 20892 USA
关键词
hematological malignancies; natural killer cells; KIR genotype; allogeneic stem cell transplantation;
D O I
10.1038/sj.leu.2404892
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Natural killer (NK) cells are the first lymphocytes to recover after allogeneic stem cell transplantation (SCT) and can exert powerful graft-versus-leukemia(GVL) effects determining transplant outcome. Conditions governing NK cell alloreactivity and the role of NK recovery in sibling SCT are not well defined. NK cells on day 30 post-transplant (NK30) were measured in 54 SCT recipients with leukemia and donor and recipient killer immunoglobulin-like receptor (KIR) genotype determined. In univariate analysis, donor KIR genes 2DL5A, 2DS1, 3DS1 ( positive in 46%) and higher numbers of inhibitory donor KIR correlated with higher NK30 counts and were associated with improved transplant outcome. NK30 counts also correlated directly with the transplant CD34 cell dose and inversely with the CD3+ cell dose. In multivariate analysis, the NK30 emerged as the single independent determinant of transplant outcome. Patients with NK30 > 150/mu l had less relapse (HR 18.3, P =0.039), acute graft-versus-host disease ( HR 3.2, P =0.03), non-relapse mortality ( HR 10.7, P =0.028) and improved survival ( HR 11.4, P =0.03). Results suggest that T cell-depleted SCT might be improved and the GVL effect enhanced by selecting donors with favorable KIR genotype, and by optimizing CD34 and CD3 doses.
引用
收藏
页码:2145 / 2152
页数:8
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