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树突状细胞中的白细胞介素-2/白细胞介素-2受体途径调节其细胞因子合成谱及其激活同种异体CD4+T淋巴细胞的能力。

[IL-2/IL-2R pathway in dendritic cell modulates both their cytokine synthesis profiles and their capacity to activate allogeneic CD4+ T lymphocytes].

作者信息

Mnasria K, Lagaraine C, Manaa J, Lebranchu Y, Oueslati R

机构信息

UR immuno microbiologie environnementale et cancérogenèse, faculté des sciences de Bizerte, Tunisie.

出版信息

Pathol Biol (Paris). 2011 Jun;59(3):e29-35. doi: 10.1016/j.patbio.2009.03.002. Epub 2009 Apr 16.

DOI:10.1016/j.patbio.2009.03.002
PMID:19375249
Abstract

The results provide new insights into the role of IL-2/IL-2R pathway in DC. We report that stimulation of human monocyte-derived DC with LPS strongly upregulated CD25 (α chain of the IL-2R) expression. In addition, by using a humanized monoclonal antibody against CD25, we demonstrated that the IL-2 signalling in DC upregulated both IL-12 and γIFN production but decreased IL-10 synthesis. Anti-CD25 treatment reduced the ability of LPS-DC to induce allogeneic CD4(+) T cell proliferation as compared to LPS-matured DC. In addition, LPS-matured DC treated with IL-2 had a higher allostimulatory capacity compared to LPS-DC. We also found that LPS-matured DC produced IL-2. Thus, IL-2 seems to contribute actively to DC activation through an autocrine pathway. Moreover, IL-2 pathway in DC is involved in T helper priming. These findings might be useful for protocols in cellular therapy and a valuable tool to understand graft rejection versus the acquisition of peripheral tolerance.

摘要

这些结果为白细胞介素-2/白细胞介素-2受体(IL-2/IL-2R)通路在树突状细胞(DC)中的作用提供了新的见解。我们报告称,用脂多糖(LPS)刺激人单核细胞衍生的DC可强烈上调CD25(IL-2R的α链)的表达。此外,通过使用抗CD25的人源化单克隆抗体,我们证明DC中的IL-2信号传导上调了IL-12和γ干扰素的产生,但降低了IL-10的合成。与LPS成熟的DC相比,抗CD25处理降低了LPS-DC诱导同种异体CD4(+) T细胞增殖的能力。此外,与LPS-DC相比,用IL-2处理的LPS成熟的DC具有更高的同种异体刺激能力。我们还发现LPS成熟的DC产生IL-2。因此,IL-2似乎通过自分泌途径积极促进DC的激活。此外,DC中的IL-2通路参与辅助性T细胞的启动。这些发现可能对细胞治疗方案有用,并且是理解移植排斥与外周耐受获得的有价值工具。

相似文献

1
[IL-2/IL-2R pathway in dendritic cell modulates both their cytokine synthesis profiles and their capacity to activate allogeneic CD4+ T lymphocytes].树突状细胞中的白细胞介素-2/白细胞介素-2受体途径调节其细胞因子合成谱及其激活同种异体CD4+T淋巴细胞的能力。
Pathol Biol (Paris). 2011 Jun;59(3):e29-35. doi: 10.1016/j.patbio.2009.03.002. Epub 2009 Apr 16.
2
Anti-CD25 antibodies affect cytokine synthesis pattern of human dendritic cells and decrease their ability to prime allogeneic CD4+ T cells.抗CD25抗体影响人树突状细胞的细胞因子合成模式,并降低其激活同种异体CD4+T细胞的能力。
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Anti CD25 treatment of human dendritic cells modulates both their cytokine synthesis profiles and their capacity to activate allogeneic CD4 T cells: a potential tolerogenic effect.抗CD25治疗人树突状细胞可调节其细胞因子合成谱及其激活同种异体CD4 T细胞的能力:一种潜在的致耐受性效应。
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Role of the cytokine environment and cytokine receptor expression on the generation of functionally distinct dendritic cells from human monocytes.细胞因子环境和细胞因子受体表达在从人单核细胞生成功能不同的树突状细胞中的作用。
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Dendritic cells partially abrogate the regulatory activity of CD4+CD25+ T cells present in the human peripheral blood.树突状细胞部分消除了人外周血中存在的CD4+CD25+ T细胞的调节活性。
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CD40 engagement strongly induces CD25 expression on porcine dendritic cells and polarizes the T cell immune response toward Th1.CD40的激活强烈诱导猪树突状细胞上CD25的表达,并使T细胞免疫反应向Th1极化。
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Bone marrow-derived immature dendritic cells prime in vivo alloreactive T cells for interleukin-4-dependent rejection of major histocompatibility complex class II antigen-disparate cardiac allograft.骨髓来源的未成熟树突状细胞在体内使同种异体反应性T细胞致敏,以实现对主要组织相容性复合体II类抗原不相合心脏移植的白细胞介素-4依赖性排斥反应。
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Secretion of interleukin-10 or interleukin-12 by LPS-activated dendritic cells is critically dependent on time of stimulus relative to initiation of purified DC culture.脂多糖激活的树突状细胞分泌白细胞介素-10或白细胞介素-12,这严重依赖于相对于纯化树突状细胞培养开始的刺激时间。
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