CD33
微小残留病
干细胞
髓系白血病
造血
医学
祖细胞
癌症研究
免疫学
白血病
单克隆抗体
肿瘤科
白细胞介素-3受体
抗体
川地34
生物
遗传学
作者
Linde M. Morsink,Roland B. Walter,Gert J. Ossenkoppele
出处
期刊:Blood Reviews
[Elsevier]
日期:2019-03-01
卷期号:34: 26-33
被引量:41
标识
DOI:10.1016/j.blre.2018.10.003
摘要
CLEC12A has recently been identified as an antigen, expressed on leukemic stem cells and leukemic blasts. Given the fact that this expression profile seems stable throughout diagnosis, treatment and relapse on leukemic blasts and leukemic stem cells, CLEC12A can be considered a highly potent and reliable marker for the detection of measurable residual disease and therefore applicable for risk stratification and prognostication in AML. Low CLEC12A expression on leukemic blasts seems to be independently associated with lower likelihood of achieving complete remission after 1 cycle of induction chemotherapy, shorter event free survival, as well as overall survival, indicating potential prognostic properties of CLEC12A expression itself. Lack of expression on the normal hematopoietic stem and progenitor cells, in contrast to CD123 and CD33, might result in less toxicity regarding cytopenias, making CLEC12A an interesting target for innovating immunotherapies, including monoclonal and bispecific antibodies, antibody-drug conjugates and CAR-T cells therapy.
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