Publication | Open Access
CD99 is a therapeutic target on disease stem cells in myeloid malignancies
159
Citations
59
References
2017
Year
Cell TherapyMixed-phenotype Acute LeukemiaMyeloid MalignanciesImmunologyImmunotherapyTumor BiologyMyeloid NeoplasiaHematological MalignancyAcute Myeloid LeukemiaMds CellsHematologyStem Cell MobilizationStem Cell TraffickingStem CellsCell TransplantationHealth SciencesDisease Stem CellsCell BiologyTumor MicroenvironmentMds Stem CellsMyelopoiesisMalignant Blood DisorderStem Cell ResearchMedicine
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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