Circulating CD56bright NK cells inversely correlate with survival of melanoma patients

被引:52
作者
de Jonge, Kaat [1 ]
Ebering, Anna [1 ]
Nassiri, Sina [1 ,3 ]
Maby-El Hajjami, Helene [1 ]
Ouertatani-Sakouhi, Hajer [1 ]
Baumgaertner, Petra [1 ]
Speiser, Daniel E. [1 ,2 ]
机构
[1] Univ Lausanne, Dept Fundamental Oncol, Epalinges, Switzerland
[2] Univ Hosp Ctr CHUV, Dept Oncol, Lausanne, Switzerland
[3] SIB, Batiment Genopode, Lausanne, Switzerland
关键词
NATURAL-KILLER-CELLS; METASTATIC MELANOMA; PROGNOSTIC-SIGNIFICANCE; CANCER; EXPRESSION; RECEPTORS; RESPONSES; NKG2D;
D O I
10.1038/s41598-019-40933-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The roles of NK cells in human melanoma remain only partially understood. We characterized NK cells from peripheral blood ex vivo by flow cytometry obtained from late stage (III/IV) melanoma patients. Interestingly, we found that the abundance of CD56(bright) NK cells negatively correlate with overall patient survival, together with distant metastases, in a multivariate cox regression analysis. The patients' CD56(bright) NK cells showed upregulation of CD11a, CD38 and CD95 as compared to healthy controls, pointing to an activated phenotype as well as a possible immune regulatory role in melanoma patients. After stimulation in vitro, CD56(bright) NK cells produced less TNF alpha and GMCSF in patients than controls. Furthermore, IFN gamma production by the CD56(bright) NK cells correlated inversely with overall survival. Our results highlight that abundance and function of CD56(bright) NK cells are associated with melanoma patient survival, emphasizing the potential of NK cell subsets for biomarker discovery and future therapeutic targeting.
引用
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页数:10
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