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红参通过调节髓源抑制细胞对 T 细胞的刺激作用。

T Cell Stimulatory Effects of Korean Red Ginseng through Modulation of Myeloid-Derived Suppressor Cells.

机构信息

College of Pharmacy, Chung-Ang University, Seoul 156-756, Korea.

出版信息

J Ginseng Res. 2011 Nov;35(4):462-70. doi: 10.5142/jgr.2011.35.4.462.

Abstract

Myeloid-derived suppressor cells (MDSCs) actively suppress immune cells and have been considered as an impediment to successful cancer immunotherapy. Many approaches have been made to overcome such immunosuppressive factors and to exert effective anti-tumor effects, but the possibility of using medicinal plants for this purpose has been overlooked. Korean red ginseng (KRG) is widely known to possess a variety of pharmacological properties, including immunoboosting and anti-tumor activities. However, little has been done to assess the anti-tumor activity of KRG on MDSCs. Therefore, we examined the effects of KRG on MDSCs in tumor-bearing mice and evaluated immunostimulatory and anti-tumor activities of KRG through MDSC modulation. The data show that intraperitoneal administration of KRG compromises MDSC function and induces T cell proliferation and the secretion of IL-2 and IFN-γ, while it does not exhibit direct cytotoxicity on tumor cells and reduced MDSC accumulation. MDSCs isolated from KRG-treated mice also express significantly lower levels of inducible nitric oxide synthase and IL-10 accompanied by a decrease in nitric oxide production compared with control. Taken together, the present study demonstrates that KRG enhances T cell function by inhibiting the immunosuppressive activity of MDSCs and suggests that although KRG alone does not exhibit direct anti-tumor effects, the use of KRG together with conventional chemo- or immunotherapy may provide better outcomes to cancer patients through MDSC modulation.

摘要

髓源抑制性细胞(MDSCs)能主动抑制免疫细胞,被认为是癌症免疫治疗成功的障碍。为了克服这种免疫抑制因素并发挥有效的抗肿瘤作用,已经提出了许多方法,但人们忽视了利用药用植物来达到这一目的的可能性。众所周知,红参(KRG)具有多种药理作用,包括免疫增强和抗肿瘤活性。然而,很少有人评估 KRG 对 MDSC 的抗肿瘤活性。因此,我们在荷瘤小鼠中研究了 KRG 对 MDSC 的影响,并通过 MDSC 调节评估了 KRG 的免疫刺激和抗肿瘤活性。数据表明,腹腔内给予 KRG 会损害 MDSC 的功能,并诱导 T 细胞增殖以及 IL-2 和 IFN-γ的分泌,而 KRG 对肿瘤细胞没有直接的细胞毒性作用,也减少了 MDSC 的积累。与对照组相比,从 KRG 处理的小鼠中分离出的 MDSC 表达的诱导型一氧化氮合酶和 IL-10 水平显著降低,同时一氧化氮的产生也减少。综上所述,本研究表明 KRG 通过抑制 MDSC 的免疫抑制活性来增强 T 细胞功能,并提示尽管 KRG 本身没有直接的抗肿瘤作用,但将 KRG 与常规化疗或免疫疗法联合使用,可能通过 MDSC 调节为癌症患者提供更好的治疗效果。

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