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霉酚酸上调树突状细胞上B7-DC的表达,这与树突状细胞的异基因刺激能力受损有关。

Mycophenolic acid upregulates B7-DC expression on dendritic cells, which is associated with impaired allostimulatory capacity of dendritic cells.

作者信息

Geng L, Jiang G, Xie H, Fang Y, Dong S, Chen Y, Shen M, Zheng S

机构信息

Key Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Transplant Proc. 2006 Jun;38(5):1622-4. doi: 10.1016/j.transproceed.2006.02.093.

Abstract

In addition to its effects on lymphocytes, mycophenolic acid (MPA) may inhibit the allostimulatory capacity of dendritic cells (DC) via unknown mechanisms. B7-H1 and B7-DC surface markers on DC negatively regulate T-cell responses via the receptor PD-1. In this study, we sought to investigate whether B7-H1 and B7-DC are responsible for the inhibitory functions of MPA on DC. Mouse bone marrow-derived DC were cultured with recombinant granulocyte macrophage colony-stimulating factor (GM-CSF) and interleukin (IL)-4 in the presence or absence of MPA (0.01 micromol and 0.1 micromol). The DC phenotype was assessed by flow cytometry, their immunostimulatory capacity measured by mixed lymphocyte reaction (MLR), and cytokine production by ELISA. The results showed that MPA not only inhibited the expression of major histocompatibility complex (MHC) class II and costimulatory molecules CD80 and CD86 but upregulated B7-DC expression on mature DC induced by LPS. These findings were associated with a reduced allostimulatory ability and an altered cytokine secretion pattern of DC. Thus, we suggest that MPA upregulates B7-DC expression during DC maturation induced by LPS in vitro, an effect that may be responsible for MPA-mediated inhibitory effects on the allostimulatory capacity of DC.

摘要

除了对淋巴细胞有作用外,霉酚酸(MPA)可能通过未知机制抑制树突状细胞(DC)的共刺激能力。DC上的B7-H1和B7-DC表面标志物通过受体PD-1负向调节T细胞反应。在本研究中,我们试图探究B7-H1和B7-DC是否介导了MPA对DC的抑制功能。将小鼠骨髓来源的DC在存在或不存在MPA(0.01微摩尔和0.1微摩尔)的情况下,与重组粒细胞巨噬细胞集落刺激因子(GM-CSF)和白细胞介素(IL)-4一起培养。通过流式细胞术评估DC表型,通过混合淋巴细胞反应(MLR)测量其免疫刺激能力,并通过酶联免疫吸附测定(ELISA)检测细胞因子产生。结果表明,MPA不仅抑制主要组织相容性复合体(MHC)II类分子以及共刺激分子CD80和CD86的表达,还上调了由脂多糖(LPS)诱导的成熟DC上B7-DC的表达。这些发现与DC的共刺激能力降低以及细胞因子分泌模式改变有关。因此,我们认为MPA在体外LPS诱导的DC成熟过程中上调B7-DC表达,这一效应可能是MPA介导的对DC共刺激能力产生抑制作用的原因。

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