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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Ecto-5′-Nucleotidase (CD73) Regulates the Survival of CD8 T Cells
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Ecto-5′-Nucleotidase (CD73) Regulates the Survival of CD8 T Cells

机译:EcTO-5'-核苷酸酶(CD73)调节CD8 T细胞的存活

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Ecto-5′-nucleotidase (CD73) is an enzyme present on the surface of tumor cells whose primary described function is the production of extracellular adenosine. Due to the immunosuppressive properties of adenosine, CD73 is being investigated as a target for new antitumor therapies. We and others have described that CD73 is present at the surface of different CD8 T cell subsets. Nonetheless, there is limited information as to whether CD73 affects CD8 T cell proliferation and survival. In this study, we assessed the impact of CD73 deficiency on CD8 T cells by analyzing their proliferation and survival in antigenic and homeostatic conditions. Results obtained from adoptive transfer experiments demonstrate a paradoxical role of CD73. On one side, it favors the expression of interleukin-7 receptor α chain on CD8 T cells and their homeostatic survival; on the other side, it reduces the survival of activated CD8 T cells under antigenic stimulation. Also, upon in vitro antigenic stimulation, CD73 decreases the expression of interleukin-2 receptor α chain and the anti-apoptotic molecule Bcl-2, findings that may explain the reduced CD8 T cell survival observed in this condition. These results indicate that CD73 has a dual effect on CD8 T cells depending on whether they are subject to an antigenic or homeostatic stimulus, and thus, special attention should be given to these aspects when considering CD73 blockade in the design of novel antitumor therapies.
机译:EcTO-5'-核苷酸酶(CD73)是肿瘤细胞表面存在的酶,其主要描述的功能是细胞外腺苷的产生。由于腺苷的免疫抑制性质,正在研究CD73作为新的抗肿瘤疗法的靶标。我们和其他人已经描述了CD73存在于不同CD8 T小区子集的表面。尽管如此,关于CD73是否影响CD8 T细胞增殖和生存的信息有限。在这项研究中,我们通过分析抗原和稳态条件的增殖和生存来评估CD73缺乏对CD8 T细胞的影响。从过养转移实验获得的结果表明了CD73的矛盾作用。一方面,它有利于白细胞介素-7受体α链对CD8 T细胞的表达及其稳态存活;在另一边,它降低了抗原刺激下活化CD8 T细胞的存活。此外,在体外抗原刺激后,CD73降低白细胞介素-2受体α链和抗凋亡分子BCL-2的表达,调查结果可以解释在这种情况下观察到的CD8 T细胞存活率降低。这些结果表明,CD73对CD8 T细胞对CD8 T细胞具有双重影响,这取决于它们是否受到抗原或稳态刺激,因此在考虑CD73封锁在新的抗肿瘤疗法的设计时,应特别注意这些方面。

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