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前沿:人CD4+CD25+ T细胞抑制树突状细胞的成熟和抗原呈递功能。

Cutting edge: human CD4+CD25+ T cells restrain the maturation and antigen-presenting function of dendritic cells.

作者信息

Misra Namita, Bayry Jagadeesh, Lacroix-Desmazes Sébastien, Kazatchkine Michel D, Kaveri Srini V

机构信息

Institut National de la Santé et de la Recherche Médicale, Unité 430, and Université Pierre et Marie Curie, Centre de Recherches Biomedicales des Cordeliers, Paris, France.

出版信息

J Immunol. 2004 Apr 15;172(8):4676-80. doi: 10.4049/jimmunol.172.8.4676.

Abstract

The characteristics and functions of CD4(+)CD25(+) regulatory cells have been well defined in murine and human systems. However, the interaction between CD4(+)CD25(+) T cells and dendritic cells (DC) remains unclear. In this study, we examined the effect of human CD4(+)CD25(+) T cells on maturation and function of monocyte-derived DC. We show that regulatory T cells render the DC inefficient as APCs despite prestimulation with CD40 ligand. This effect was marginally reverted by neutralizing Abs to TGF-beta. There was an increased IL-10 secretion and reduced expression of costimulatory molecules in DC. Thus, in addition to direct suppressor effect on CD4(+) T cells, regulatory T cells may modulate the immune response through DC.

摘要

CD4(+)CD25(+)调节性细胞的特征和功能在小鼠和人类系统中已得到明确界定。然而,CD4(+)CD25(+) T细胞与树突状细胞(DC)之间的相互作用仍不清楚。在本研究中,我们检测了人CD4(+)CD25(+) T细胞对单核细胞来源的DC成熟和功能的影响。我们发现,尽管用CD40配体进行了预刺激,但调节性T细胞使DC作为抗原呈递细胞(APC)的效率降低。用抗TGF-β中和抗体可使这种效应略有逆转。DC中IL-10分泌增加,共刺激分子表达减少。因此,除了对CD4(+) T细胞的直接抑制作用外,调节性T细胞可能通过DC调节免疫反应。

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