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利用动物模型剖析关节炎的遗传复杂性。

Dissection of the genetic complexity of arthritis using animal models.

作者信息

Holmdahl Rikard

机构信息

Medical Inflammation Research, BMC I11, Lund University, S-22184 Lund, Sweden.

出版信息

Immunol Lett. 2006 Mar 15;103(2):86-91. doi: 10.1016/j.imlet.2005.10.025. Epub 2005 Nov 18.

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease directed towards peripheral joints. As all common diseases it is associated with several genes and a multitude of environmental factors. In addition, in similarity with most other complex diseases, it is defined only on the basis of clinical signs and symptoms, it is therefore more properly classified as a syndrome rather than a distinct disease entity. This complexity of RA has led to difficulties in finding the underlying genes. In spite of large efforts it is still only the MHC class II region that reaches genome wide significance in confirmed studies. However, this has been known for decades and we are still unable to conclusively identify the underlying gene/s. We hypothesize that an MHC class II gene is involved and although we have detailed knowledge on both structure and function we do not know its possible pathogenic role in RA. In this review I will argue for the usefulness of animal models as a tool to identify genes and pathways associated with disease. The examples to be discussed are genes controlling the oxidative burst pathways and MHC class II genes.

摘要

类风湿性关节炎(RA)是一种针对外周关节的慢性炎症性疾病。与所有常见疾病一样,它与多个基因及众多环境因素相关。此外,与大多数其他复杂疾病类似,它仅根据临床体征和症状来定义,因此更确切地应归类为一种综合征而非一种独特的疾病实体。RA的这种复杂性导致在寻找潜在基因方面存在困难。尽管付出了巨大努力,但在已确认的研究中,目前仍只有MHC II类区域达到全基因组显著性。然而,这一情况已为人所知数十年,我们仍然无法最终确定潜在的基因。我们推测MHC II类基因与之相关,尽管我们对其结构和功能都有详细了解,但我们并不清楚它在RA中可能的致病作用。在这篇综述中,我将论证动物模型作为识别与疾病相关的基因和通路的工具的有用性。将要讨论的例子是控制氧化爆发通路的基因和MHC II类基因。

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