造血
干细胞
癌症研究
髓系白血病
癌症干细胞
医学
白血病
骨髓增生异常综合症
髓样
免疫学
造血干细胞
生物
骨髓
细胞生物学
作者
Stephen S. Chung,William Eng,Wenhuo Hu,Mona Khalaj,Francine E. Garrett-Bakelman,Montreh Tavakkoli,Ross L. Levine,Martin Carroll,Virginia M. Klimek,Ari Melnick,Christopher Y. Park
标识
DOI:10.1126/scitranslmed.aaj2025
摘要
Acute myeloid leukemia (AML) and the myelodysplastic syndromes (MDS) are initiated and sustained by self-renewing malignant stem cells; thus, eradication of AML and MDS stem cells is required for cure. We identified CD99 as a cell surface protein frequently overexpressed on AML and MDS stem cells. Expression of CD99 allows for prospective separation of leukemic stem cells (LSCs) from functionally normal hematopoietic stem cells in AML, and high CD99 expression on AML blasts enriches for functional LSCs as demonstrated by limiting dilution xenotransplant studies. Monoclonal antibodies (mAbs) targeting CD99 induce the death of AML and MDS cells in a SARC family kinase-dependent manner in the absence of immune effector cells or complement, and anti-CD99 mAbs exhibit antileukemic activity in AML xenografts. These data establish CD99 as a marker of AML and MDS stem cells, as well as a promising therapeutic target in these disorders.
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