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Natural Killer Immunotherapy for Minimal Residual Disease Eradication Following Allogeneic Hematopoietic Stem Cell Transplantation in Acute Myeloid Leukemia
被引:18
|作者:
Hattori, Norimichi
[1
]
Nakamaki, Tsuyoshi
[1
]
机构:
[1] Showa Univ, Sch Med, Dept Med, Div Hematol, Tokyo 1428555, Japan
关键词:
natural killer cell;
immunotherapy;
allogeneic hematopoietic stem cell transplantation;
acute myeloid leukemia;
immune checkpoint;
bispecific and trispecific killer cell engagers;
chimeric antigen receptors;
IMMUNE CHECKPOINT INHIBITORS;
DONOR LYMPHOCYTE INFUSIONS;
VERSUS-HOST-DISEASE;
IN-VIVO EXPANSION;
NK CELLS;
ACQUIRED-RESISTANCE;
THERAPEUTIC ANTIBODY;
CLINICAL-TRIAL;
TREAT RELAPSE;
PHASE-II;
D O I:
10.3390/ijms20092057
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The most common cause of death in patients with acute myeloid leukemia (AML) who receive allogeneic hematopoietic stem cell transplantation (allo-HSCT) is AML relapse. Therefore, additive therapies post allo-HSCT have significant potential to prevent relapse. Natural killer (NK)-cell-based immunotherapies can be incorporated into the therapeutic armamentarium for the eradication of AML cells post allo-HSCT. In recent studies, NK cell-based immunotherapies, the use of adoptive NK cells, NK cells in combination with cytokines, immune checkpoint inhibitors, bispecific and trispecific killer cell engagers, and chimeric antigen receptor-engineered NK cells have all shown antitumor activity in AML patients. In this review, we will discuss the current strategies with these NK cell-based immunotherapies as possible therapies to cure AML patients post allo-HSCT. Additionally, we will discuss various means of immune escape in order to further understand the mechanism of NK cell-based immunotherapies against AML.
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页数:17
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