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甘露聚糖结合凝集素在炎症性肠病的诊断中有作用吗?

Is there a role for mannan-binding lectin in the diagnosis of inflammatory bowel disease?

机构信息

Institute of Laboratory Medicine and Pathobiochemistry, Charité University Medicine Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.

出版信息

Immunogenetics. 2010 Apr;62(4):231-5. doi: 10.1007/s00251-010-0429-0. Epub 2010 Feb 25.

Abstract

Mannan-binding lectin (MBL) activates the lectin-complement pathway as part of the innate immune defence by binding to the surface of microorganisms. Therefore, MBL2 presents an interesting candidate gene for the inflammatory bowel diseases, ulcerative colitis (UC) and Crohn's disease (CD). In our study, we evaluated the MBL serum concentrations and genotypes for diagnostic and classification purposes of patients with CD and UC. The MBL serum concentration was analysed in 98 CD patients and in 83 UC patients. In total, 82 patients with inflammatory rheumatic disorders and 189 healthy individuals served as controls. All study subjects were genotyped for the MBL2 polymorphisms G54D, G57E and R52C and the NOD2 (CARD15) mutations R702W, G908R and L1007fsinsC. Neither the median MBL serum concentration nor the MBL2 genotype distribution differed significantly between cohorts. Measurement of MBL serum concentrations offers no benefit for the diagnosis of CD or UC.

摘要

甘露聚糖结合凝集素 (MBL) 通过与微生物表面结合,激活凝集素-补体途径,作为先天免疫防御的一部分。因此,MBL2 是炎症性肠病(溃疡性结肠炎 (UC) 和克罗恩病 (CD) 的一个有趣的候选基因。在我们的研究中,我们评估了 MBL 血清浓度和基因型,以用于 CD 和 UC 患者的诊断和分类目的。分析了 98 例 CD 患者和 83 例 UC 患者的 MBL 血清浓度。总共 82 例炎症性风湿性疾病患者和 189 名健康个体作为对照。所有研究对象均对 MBL2 多态性 G54D、G57E 和 R52C 以及 NOD2 (CARD15) 突变 R702W、G908R 和 L1007fsinsC 进行了基因分型。MBL 血清浓度的中位数或 MBL2 基因型分布在队列之间没有显著差异。MBL 血清浓度的测量对 CD 或 UC 的诊断没有益处。

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