Enhancing Natural Killer Cell-Mediated Cancer Immunotherapy by the Biological Macromolecule Nocardia rubra Cell-Wall Skeleton.

Pathology oncology research : POR Pub Date : 2022-08-30 eCollection Date: 2022-01-01 DOI:10.3389/pore.2022.1610555
Jie Wu, Baojun He, Miao Miao, Xibin Han, Hongyan Dai, Heng Dou, Yanqiu Li, Xiaoqing Zhang, Guangchuan Wang
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引用次数: 4

Abstract

The biological macromolecule Nocardia rubra cell-wall skeleton (Nr-CWS) has well-established immune-stimulating and anti-tumor activities. However, the role of Nr-CWS on natural killer (NK) cells remains unclear. Here, we explore the function and related mechanisms of Nr-CWS on NK cells. Using a tumor-bearing model, we show that Nr-CWS has slightly effect on solid tumor. In addition, using a tumor metastasis model, we show that Nr-CWS suppresses the lung metastasis induced by B16F10 melanoma cells in mice, which indicates that Nr-CWS may up-regulate the function of NK cells. Further investigation demonstrated that Nr-CWS can increase the expression of TRAIL and FasL on spleen NK cells from Nr-CWS treated B16F10 tumor metastasis mice. The spleen index and serum levels of TNF-α, IFN-γ, and IL-2 in B16F10 tumor metastasis mice treated with Nr-CWS were significantly increased. In vitro, the studies using purified or sorted NK cells revealed that Nr-CWS increases the expression of CD69, TRAIL, and FasL, decreases the expression of CD27, and enhances NK cell cytotoxicity. The intracellular expression of IFN-γ, TNF-α, perforin (prf), granzyme-B (GrzB), and secreted TNF-α, IFN-γ, IL-6 of the cultured NK cells were significantly increased after treatment with Nr-CWS. Overall, the findings indicate that Nr-CWS could suppress the lung metastasis induced by B16F10 melanoma cells, which may be exerted through its effect on NK cells by promoting NK cell terminal differentiation (CD27lowCD11bhigh), and up-regulating the production of cytokines and cytotoxic molecules.

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利用生物大分子红诺卡菌细胞壁骨架增强自然杀伤细胞介导的癌症免疫治疗。
生物大分子红诺卡菌细胞壁骨架(Nr-CWS)具有良好的免疫刺激和抗肿瘤活性。然而,Nr-CWS对自然杀伤(NK)细胞的作用尚不清楚。在此,我们探讨了Nr-CWS对NK细胞的作用及其相关机制。通过荷瘤模型,我们发现Nr-CWS对实体瘤有轻微的影响。此外,通过肿瘤转移模型,我们发现Nr-CWS抑制小鼠B16F10黑色素瘤细胞诱导的肺转移,这表明Nr-CWS可能上调NK细胞的功能。进一步研究表明,Nr-CWS可增加B16F10肿瘤转移小鼠脾NK细胞TRAIL和FasL的表达。Nr-CWS治疗B16F10肿瘤转移小鼠脾脏指数及血清TNF-α、IFN-γ、IL-2水平均显著升高。体外纯化或分选NK细胞的研究发现,Nr-CWS增加CD69、TRAIL和FasL的表达,降低CD27的表达,增强NK细胞的细胞毒性。经n - cws处理后,培养的NK细胞细胞内IFN-γ、TNF-α、穿孔素(prf)、颗粒酶- b (GrzB)表达及分泌的TNF-α、IFN-γ、IL-6均显著升高。综上所述,Nr-CWS可抑制B16F10黑色素瘤细胞诱导的肺转移,其作用机制可能是通过促进NK细胞末端分化(CD27lowCD11bhigh),上调细胞因子和细胞毒分子的产生,从而对NK细胞产生抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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