期刊
LEUKEMIA
卷 26, 期 3, 页码 465-474出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/leu.2011.239
关键词
CML; NK cells; BCR-ABL
资金
- program Innovative Medical Research (IMF) [CH 220913]
- German Research Foundation (DFG) at the University Hospital Muenster [KO 2155/2-2]
- MRC [G0600782] Funding Source: UKRI
- Medical Research Council [G0600782] Funding Source: researchfish
Although BCR-ABL+ stem cells in chronic myeloid leukemia (CML) resist elimination by targeted pharmacotherapy in most patients, immunological graft-versus-leukemia effects can cure the disease. Besides cytotoxic T cells, natural killer (NK) cells may have a role in immune control of CML. Here, we explored the functionality of NK cells in CML patients and in a transgenic inducible BCR-ABL mouse model. Compared with controls, NK-cell proportions among lymphocytes were decreased at diagnosis of CML and did not recover during imatinib-induced remission for 10-34 months. Functional experiments revealed limited in vitro expansion of NK cells from CML patients and a reduced degranulation response to K562 target cells both at diagnosis and during imatinib therapy. Consistent with the results in human CML, relative numbers of NK1.1+ NK cells were reduced following induction of BCR-ABL expression in mice, and the defects persisted after BCR-ABL reversion. Moreover, target-induced degranulation by expanded BCR-ABL+ NK cells was compromised. We conclude that CML is associated with quantitative and functional defects within the NK-cell compartment, which is reproduced by induced BCR-ABL expression in mice. Further work will aim at identifying the mechanisms of NK-cell deficiency in CML and at developing strategies to exploit NK cells for immunotherapy. Leukemia (2012) 26, 465-474; doi:10.1038/leu.2011.239; published online 9 September 2011
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