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携带NOD2 3020insC突变的克罗恩病患者树突状细胞功能受损。

Impaired dendritic cell function in Crohn's disease patients with NOD2 3020insC mutation.

作者信息

Kramer Matthijs, Netea Mihai G, de Jong Dirk J, Kullberg Bart Jan, Adema Gosse J

机构信息

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Geert Grooteplein 28, 6525 GA, Nijmegen, The Netherlands.

出版信息

J Leukoc Biol. 2006 Apr;79(4):860-6. doi: 10.1189/jlb.0805484. Epub 2006 Feb 3.

Abstract

The nucleotide oligomerization domain 2 (NOD2) 3020insC (NOD2fs) mutation increases susceptibility to Crohn's disease (CD), but the mechanism remains controversial. Loss-of-function and gain-of-function phenotypes have been described as a result of NOD2fs. Here, we show that dendritic cells (DC) derived from CD patients homozygous for this mutation respond normally to purified Toll-like receptor (TLR) ligands but fail to up-regulate the costimulatory molecules CD80 and CD86 in response to the NOD2 ligand muramyl dipeptide (MDP). Moreover, they lack MDP-induced enhancement of TLR-mediated tumor necrosis factor alpha, interleukin (IL)-12, and IL-10 production, which is observed in control DC with intact NOD2. These data indicate that the NOD2fs mutation results in a loss-of-function phenotype in human myeloid DC and imply decreased immune regulation by IL-10 as a possible mechanism for this mutation in CD.

摘要

核苷酸寡聚化结构域2(NOD2)3020insC(NOD2fs)突变增加了患克罗恩病(CD)的易感性,但其机制仍存在争议。功能丧失和功能获得表型已被描述为NOD2fs的结果。在此,我们表明,源自该突变纯合子的CD患者的树突状细胞(DC)对纯化的Toll样受体(TLR)配体反应正常,但对NOD2配体胞壁酰二肽(MDP)无反应,无法上调共刺激分子CD80和CD86。此外,它们缺乏MDP诱导的TLR介导的肿瘤坏死因子α、白细胞介素(IL)-12和IL-10产生的增强,而在具有完整NOD2的对照DC中可观察到这种增强。这些数据表明,NOD2fs突变导致人类髓样DC出现功能丧失表型,并暗示IL-10介导的免疫调节降低可能是CD中该突变的一种机制。

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