Targeting CLL-1 for acute myeloid leukemia therapy

被引:69
|
作者
Ma, Hongbing [1 ]
Padmanabhan, Iyer Swaminathan [2 ]
Parmar, Simrit [2 ]
Gong, Yuping [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Hematol, Chengdu, Sichuan, Peoples R China
[2] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
关键词
Acute myeloid leukemia; CLL-1; CLEC12A; DCAL-2; hMICL; CD371; LECTIN-LIKE MOLECULE-1; MINIMAL RESIDUAL DISEASE; BISPECIFIC ANTIBODY; MICL CLEC12A; ANTIGEN; RECEPTORS; MARKER; IMMUNOTHERAPY; INFLAMMATION; DIAGNOSIS;
D O I
10.1186/s13045-019-0726-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite major scientific discoveries and novel therapies over the past four decades, the treatment outcomes of acute myeloid leukemia (AML), especially in the adult patient population remain dismal. In the past few years, an increasing number of targets such as CD33, CD123, CLL-1, CD47, CD70, and TIM3, have been developed for immunotherapy of AML. Among them, CLL-1 has attracted the researchers' attention due to its high expression in AML while being absent in normal hematopoietic stem cell. Accumulating evidence have demonstrated CLL-1 is an ideal target for AML. In this paper, we will review the expression of CLL-1 on normal cells and AML, the value of CLL-1 in diagnosis and follow-up, and targeting CLL-1 therapy-based antibody and chimeric antigen receptor T cell therapy as well as providing an overview of CLL-1 as a target for AML.
引用
收藏
页数:11
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