NK cell expression of natural cytotoxicity receptors may determine relapse risk in older AML patients undergoing immunotherapy for remission maintenance

被引:30
|
作者
Martner, Anna [1 ]
Rydstrom, Anna [1 ]
Riise, Rebecca E. [1 ]
Aurelius, Johan [1 ,2 ]
Brune, Mats [2 ]
Foa, Robin [3 ]
Hellstrand, Kristoffer [1 ]
Thoren, Fredrik B. [1 ]
机构
[1] Univ Gothenburg, TIMM Lab, Sahlgrenska Canc Ctr, S-40530 Gothenburg, Sweden
[2] Univ Gothenburg, Dept Hematol, S-41345 Gothenburg, Sweden
[3] Univ Roma La Sapienza, Dept Cellular Biotechnol & Hematol, I-00161 Rome, Italy
基金
瑞典研究理事会;
关键词
acute myeloid leukemia; immunotherapy; natural killer cells; NKp30; NKp46; ACUTE MYELOID-LEUKEMIA; KILLER-CELLS; FREE SURVIVAL; ACTIVATION; INTERLEUKIN-2; HISTAMINE; THERAPY;
D O I
10.18632/oncotarget.5559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In a phase IV trial, eighty-four patients (age 18-79) with acute myeloid leukemia (AML) in first complete remission (CR) received cycles of immunotherapy with histamine dihydrochloride (HDC) and low-dose human recombinant interleukin-2 (IL-2) to prevent relapse in the post-consolidation phase. Aspects of natural killer (NK) cell biology were analyzed before and during immunotherapy with focus on outcome in older patients. In younger (<60 years old, n = 37) and older patients (> 60 years old, n = 47), treatment with HDC/IL-2 resulted in an expansion of CD56(bright) and CD16(+) NK cells in blood along with an increased NK cell expression of the natural cytotoxicity receptors (NCR) NKp30 and NKp46. In older patients, a high expression of NKp30 or NKp46 on CD16(+) NK cells before and during therapy predicted leukemia-free and overall survival. These results suggest that NK cell functions determine relapse risk and survival in older AML patients and point to biomarkers of efficacy in protocols for remission maintenance.
引用
收藏
页码:42569 / 42574
页数:6
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