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白细胞介素-10与γ干扰素协同调节树突状细胞功能。

Co-operative action of interleukin-10 and interferon-gamma to regulate dendritic cell functions.

作者信息

Yanagawa Yoshiki, Iwabuchi Kazuya, Onoé Kazunori

机构信息

Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.

出版信息

Immunology. 2009 Jul;127(3):345-53. doi: 10.1111/j.1365-2567.2008.02986.x. Epub 2008 Dec 18.

Abstract

Interleukin-10 (IL-10) and interferon-gamma (IFN-gamma) double producer is found in a subpopulation of T regulatory type 1 (Tr1) and T helper type 1 (Th1) cells. Consequently, it is of interest how IL-10 and IFN-gamma influence the immune system. However, few studies have addressed the co-operative action of these 'immunosuppressive' and 'immunostimulatory' cytokines. Here, we examine the effect of IL-10 combined with IFN-gamma on dendritic cell (DC) functions. Murine bone marrow-derived conventional DCs were stimulated with IL-10 and/or IFN-gamma for 24 hr. Tumour necrosis factor-alpha and IL-12 p40 production by DCs treated with both IL-10 and IFN-gamma was significantly lower than that by DCs treated with IL-10 or IFN-gamma alone. Major histocompatibility complex class II expression on DCs treated with both cytokines was attenuated compared with that on DCs treated with either cytokine alone. In contrast, levels of inducible nitric oxide synthase and indoleamine 2,3-dioxygenase, which appear to suppress T-cell responses and promote tolerance, in DCs treated with both cytokines were higher than those in DCs treated with IL-10 or IFN-gamma alone. Simultaneous treatment with IL-10 and IFN-gamma significantly suppressed the ability of DCs to activate CD4+ T cells compared with treatment with either cytokine. Therefore, IL-10 and IFN-gamma co-operatively suppress the immunostimulatory functions of DCs.

摘要

在1型调节性T细胞(Tr1)和1型辅助性T细胞(Th1)亚群中发现了白细胞介素10(IL-10)和干扰素-γ(IFN-γ)的双产生细胞。因此,IL-10和IFN-γ如何影响免疫系统备受关注。然而,很少有研究探讨这些“免疫抑制性”和“免疫刺激性”细胞因子的协同作用。在此,我们研究了IL-10与IFN-γ联合对树突状细胞(DC)功能的影响。用IL-10和/或IFN-γ刺激小鼠骨髓来源的常规DC 24小时。同时用IL-10和IFN-γ处理的DC产生的肿瘤坏死因子-α和IL-12 p40明显低于单独用IL-10或IFN-γ处理的DC。与单独用任何一种细胞因子处理的DC相比,同时用两种细胞因子处理的DC上主要组织相容性复合体II类分子的表达减弱。相反,同时用两种细胞因子处理的DC中诱导型一氧化氮合酶和吲哚胺2,3-双加氧酶的水平高于单独用IL-10或IFN-γ处理的DC,这两种酶似乎可抑制T细胞反应并促进免疫耐受。与单独用任何一种细胞因子处理相比,同时用IL-10和IFN-γ处理显著抑制了DC激活CD4+T细胞的能力。因此,IL-10和IFN-γ协同抑制DC的免疫刺激功能。

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