Pre-emptive immunotherapy with purified natural killer cells after haploidentical SCT: a prospective phase II study in two centers

被引:131
作者
Stern, M. [1 ]
Passweg, J. R. [1 ]
Meyer-Monard, S. [1 ]
Esser, R. [2 ]
Tonn, T. [3 ,4 ]
Soerensen, J. [2 ]
Paulussen, M. [1 ]
Gratwohl, A. [1 ]
Klingebiel, T. [2 ]
Bader, P. [2 ]
Tichelli, A. [1 ]
Schwabe, D. [2 ]
Koehl, U. [2 ,5 ,6 ]
机构
[1] Univ Basel Hosp, Div Hematol, Stem Cell Transplant Team, CH-4031 Basel, Switzerland
[2] Goethe Univ Frankfurt, D-60054 Frankfurt, Germany
[3] Red Cross Blood Donor Ctr, Frankfurt, Germany
[4] Red Cross Blood Donor Ctr, Dresden, Germany
[5] Hannover Med Sch, GMP Dev Unit, Hannover, Germany
[6] Hannover Med Sch, Cellular Therapy Ctr, Hannover, Germany
基金
瑞士国家科学基金会;
关键词
DLI; NK cells; haploidentical; leukemia; DEPLETED STEM-CELLS; NK CELLS; LYMPHOCYTE INFUSION; VIVO EXPANSION; ACUTE-LEUKEMIA; T-CELLS; TRANSPLANTATION; CYTOTOXICITY; IL-2; RECONSTITUTION;
D O I
10.1038/bmt.2012.162
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Adoptive immunotherapy with allogeneic purified natural killer (NK) cell products might exert graft-versus-tumor alloreactivity with little risk of GVHD. In a prospective phase II study in two centers, we administered purified NK cell products to high-risk patients treated with haploidentical T-cell-depleted SCT. Sixteen patients received a total of 29 NK cell infusions on days +3, +40 and +100 after transplantation. Median doses (and ranges) of infused NK- and T-cells per product were 1.21 (0.3-3.8) x 10(7)/kg and 0.03 (0.004-0.72) x 10(5)/kg, respectively. With a median follow-up of 5.8 years 4/16 patients are alive. Cause of death was relapse in five, GVHD in three, graft failure in three, and transplant related neurotoxicity in one patient. Four patients developed acute GVHD >= grade II, all receiving a total of >= 0.5 x 10(5) T cells/kg. Compared with historical controls, NK cell infusions had no apparent effect on the rates of graft failure or relapse. Adoptive transfer of allogeneic NK cells is safe and feasible, but further studies are needed to determine the optimal dose and timing of NK cell therapy. Moreover, NK cell activation/expansion may be required to attain clinical benefit, while careful consideration must be given to the number of T cells infused. Bone Marrow Transplantation (2013) 48, 433-438; doi:10.1038/bmt.2012.162; published online 3 September 2012
引用
收藏
页码:433 / 438
页数:6
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