Zhang Zhuoli, Gorman Claire, Clark Joanna M, Cope Andrew P
Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College, London, United Kingdom.
Wien Med Wochenschr. 2006 Jan;156(1-2):2-10. doi: 10.1007/s10354-005-0246-5.
Technology has advanced to the stage where it is now possible to identify genes that confer low to moderate risk of developing autoimmune diseases such as rheumatoid arthritis (RA). This has been facilitated by the growing appreciation that these hard to detect genetic signals can only be defined in large cohorts of well characterized patients. In RA, the association between disease susceptibility and genes encoded within the MHC has been known for decades. Recent studies have identified several new candidate genes that provide further insights into the molecular nature of aberrant immune responses in chronic inflammatory diseases. Here, we describe some of these new genes. Based on their known functions we propose that in a subgroup of patients with RA inheritance of allelic variants at distinct loci could lead to dysregulation of adaptive immune responses characterized by chronic, low-amplitude signaling transduced by antigen T cell receptors.
技术已经发展到现在能够识别赋予类风湿关节炎(RA)等自身免疫性疾病低至中度发病风险的基因的阶段。越来越多的人认识到,这些难以检测到的遗传信号只能在大量特征明确的患者队列中定义,这推动了这一进展。在类风湿关节炎中,疾病易感性与主要组织相容性复合体(MHC)内编码的基因之间的关联已为人所知数十年。最近的研究已经确定了几个新的候选基因,这些基因进一步揭示了慢性炎症性疾病中异常免疫反应的分子本质。在这里,我们描述其中一些新基因。基于它们已知的功能,我们提出,在一部分类风湿关节炎患者中,不同位点等位基因变体的遗传可能导致适应性免疫反应失调,其特征是由抗原T细胞受体转导的慢性、低幅度信号。