Acute myeloid leukemia targets for bispecific antibodies

被引:2
|
作者
Hoseini, S. S. [1 ]
Cheung, N. K. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, 1275 York Ave,Box 170, New York, NY 10021 USA
来源
BLOOD CANCER JOURNAL | 2017年 / 7卷
关键词
NATURAL-KILLER-CELLS; DEPENDENT CELLULAR CYTOTOXICITY; ACUTE MYELOGENOUS LEUKEMIA; ENDOTHELIAL GROWTH-FACTOR; HEMATOPOIETIC STEM-CELLS; MINIMAL RESIDUAL DISEASE; LECTIN-LIKE MOLECULE-1; RECEPTOR-ALPHA CHAIN; T-CELL; INTERLEUKIN-3; RECEPTOR;
D O I
10.1038/bcj.2017.2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite substantial gains in our understanding of the genomics of acute myelogenous leukemia (AML), patient survival remains unsatisfactory especially among the older age group. T cell-based therapy of lymphoblastic leukemia is rapidly advancing; however, its application in AML is still lagging behind. Bispecific antibodies can redirect polyclonal effector cells to engage chosen targets on leukemia blasts. When the effector cells are natural-killer cells, both antibody-dependent and antibody-independent mechanisms could be exploited. When the effectors are T cells, direct tumor cytotoxicity can be engaged followed by a potential vaccination effect. In this review, we summarize the AML-associated tumor targets and the bispecific antibodies that have been studied. The potentials and limitations of each of these systems will be discussed.
引用
收藏
页码:e522 / e522
页数:12
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