CD8+CD73+T cells in the tumor microenvironment of head and neck cancer patients are linked to diminished T cell infiltration and activation in tumor tissue

被引:10
作者
Panigrahi, Soumya [1 ]
Bazdar, Douglas A. [1 ]
Albakri, Marwah [2 ,3 ,4 ]
Ferrari, Brian [1 ]
Antonelli, Christopher J. [1 ]
Freeman, Michael L. [1 ]
Dubyak, George [5 ]
Zender, Chad [6 ]
Sieg, Scott F. [1 ]
机构
[1] Case Western Reserve Sch Med, Div Infect Dis & HIV Med, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Pathol, Cleveland, OH 44106 USA
[3] Taibah Univ, Medina, Saudi Arabia
[4] Coll Appl Med Sci, Dept Med Lab Technol, Medina, Saudi Arabia
[5] Case Western Reserve Univ, Sch Med, Dept Physiol & Biophys, Cleveland, OH 44106 USA
[6] Univ Cincinnati, MED Otolaryngol, Cincinnati, OH USA
关键词
CD73; head and neck cancer; T cells; ADENOSINE; LYMPHOCYTES; IMMUNOTHERAPY; INHIBITION; GENERATION; RECEPTORS; CARCINOMA; SURVIVAL; IMPACT; CD73;
D O I
10.1002/eji.202048626
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies have implicated a role for adenosine-dependent immunosuppression in head and neck tumor microenvironments. We describe expression of CD73, an enzyme critical to the generation of adenosine from extracellular AMP, in T cells and other cell types within human head and neck tumors. Flow cytometric analyses of tumor-infiltrating cells indicate that CD3(+)cells are the predominant source of CD73 among immune infiltrating cells and that CD73 expression, especially among CD8(+)T cells, is inversely related to indices of T cell infiltration and T cell activation in the microenvironment of head and neck tumors. We provide evidence that CD73 expression on peripheral T cells and levels of soluble CD73 in circulation are correlated with CD73 expression on CD8(+)T cells in tumors. Moreover, fluorescent microscopy studies reveal that CD8(+)CD73(+)cells are observed in close proximity to tumor cells as well as in surrounding tissue. In vitro studies with peripheral blood T cells indicate that anti-CD3-stimulation causes loss of CD73 expression, especially among cells that undergo proliferation and that exogenous AMP can impair T cell proliferation, while sustaining CD73 expression. These data suggest that CD8(+)CD73(+)T cells may be especially important mediators of immunosuppression in human head and neck cancer.
引用
收藏
页码:2055 / 2066
页数:12
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