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自然杀伤细胞炎症与结直肠癌的临床转归。

NK Cell Inflammation in the Clinical Outcome of Colorectal Carcinoma.

机构信息

Institute of Systems Medicine, University of Rome "Tor Vergata" , Rome , Italy.

Hematology, Department of Biomedicine and Prevention, University of Rome "Tor Vergata" , Rome , Italy.

出版信息

Front Med (Lausanne). 2015 May 26;2:33. doi: 10.3389/fmed.2015.00033. eCollection 2015.

Abstract

The ability of natural killer (NK) cells to provide protection against myeloid leukemia has been demonstrated in clinical settings. However, whether NK cells play a role in the clinical course of solid tumors is debated. The controversy surrounding the role of NK cells is due, at least in part, to the limited extent of NK cell infiltration found in the tumor bed. Inactivation of NK cells may explain the shortage of NK cells in the microenvironment of colorectal cancer (CRC). Upon NK cell/tumor cell interaction, tumor cells may escape NK cells by creating an immunosuppressive microenvironment, which possibly affects T-cells as well. Such an immunosuppressive microenvironment would hamper the functions of NK and T-cell and reduce NK and T-cell interactions. CRC patients with levels of tumor NK cell infiltration suitable for statistical analysis have been identified. The infiltration of the CRC microenvironment by NK cells, in combination with CD8(+) T-lymphocytes, has been shown to enhance the prognosis of CRC patients. Here, we discuss the clinicopathological role of NK cells in CRC, and present clinical data indicating a potential supporting role for NK cells in the anti-CRC effects of CD8(+) T-cells.

摘要

自然杀伤 (NK) 细胞提供针对髓系白血病保护的能力已在临床环境中得到证实。然而,NK 细胞是否在实体瘤的临床病程中发挥作用仍存在争议。围绕 NK 细胞作用的争议至少部分归因于在肿瘤床中发现的 NK 细胞浸润程度有限。NK 细胞的失活可能解释了结直肠癌 (CRC) 微环境中 NK 细胞的缺乏。在 NK 细胞/肿瘤细胞相互作用时,肿瘤细胞可能通过创建免疫抑制微环境来逃避 NK 细胞,这也可能影响 T 细胞。这种免疫抑制微环境会削弱 NK 和 T 细胞的功能,并减少 NK 和 T 细胞的相互作用。已经确定了具有适合统计分析的肿瘤 NK 细胞浸润水平的 CRC 患者。NK 细胞与 CD8(+)T 淋巴细胞一起浸润 CRC 微环境,已显示可增强 CRC 患者的预后。在这里,我们讨论了 NK 细胞在 CRC 中的临床病理作用,并提出了临床数据,表明 NK 细胞在 CD8(+)T 细胞的抗 CRC 作用中具有潜在的支持作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b1d/4469113/bf73ddc42e2d/fmed-02-00033-g001.jpg

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