Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Curr Opin Rheumatol. 2010 Mar;22(2):109-18. doi: 10.1097/BOR.0b013e328336474d.
To review the recently discovered genetic risk loci in rheumatoid arthritis (RA), the pathways they implicate, and the genetic architecture of RA.
Since 2008 investigators have identified many common genetic variants that confer disease risk through single nucleotide polymorphism genotyping studies; the list of variants will no doubt continue to expand at a rapid rate as genotyping technologies evolve and case-control sample collections continue to grow. In aggregate, these variants implicate pathways leading to NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B cells) activation, the interluekin-2 signaling pathway, and T-cell activation.
Although the effect of any individual variant is modest and even in aggregate considerably less than that of the major histocompatability complex, discovery of recent risk variants suggests immunological processes that are involved in disease pathogenesis.
最近发现的类风湿关节炎(RA)的遗传风险基因座、它们涉及的途径以及 RA 的遗传结构。
自 2008 年以来,研究人员通过单核苷酸多态性基因分型研究发现了许多常见的遗传变异,这些变异通过单核苷酸多态性基因分型研究赋予疾病风险;随着基因分型技术的发展和病例对照样本的不断增加,变异列表无疑将以更快的速度继续扩展。总的来说,这些变异涉及到 NF-κB(核因子κ轻链增强子的激活 B 细胞)激活、白细胞介素-2 信号通路和 T 细胞激活的途径。
尽管任何单个变异的影响都很小,即使综合起来也远远小于主要组织相容性复合体,但最近发现的风险变异提示涉及疾病发病机制的免疫过程。