Olofsson Peter, Holmberg Jens, Tordsson Jesper, Lu Shemin, Akerström Bo, Holmdahl Rikard
Section for Medical Inflammation Research and Department of Cell and Molecular Biology, Sölvegatan 19, I11 BMC, Lund University, S-22184 Lund, Sweden.
Nat Genet. 2003 Jan;33(1):25-32. doi: 10.1038/ng1058. Epub 2002 Dec 2.
The identification of genes underlying quantitative-trait loci (QTL) for complex diseases, such as rheumatoid arthritis, is a challenging and difficult task for the human genome project. Through positional cloning of the Pia4 QTL in rats, we found that a naturally occurring polymorphism of Ncf1 (encoding neutrophil cytosolic factor 1, a component of the NADPH oxidase complex) regulates arthritis severity. The disease-related allele of Ncf1 has reduced oxidative burst response and promotes activation of arthritogenic T cells. Pharmacological treatment with substances that activate the NADPH oxidase complex is shown to ameliorate arthritis. Hence, Ncf1 is associated with a new autoimmune mechanism leading to severe destructive arthritis, notably similar to rheumatoid arthritis in humans.
对于人类基因组计划而言,鉴定类风湿关节炎等复杂疾病的数量性状基因座(QTL)相关基因是一项具有挑战性的艰巨任务。通过对大鼠中Pia4 QTL进行定位克隆,我们发现Ncf1(编码中性粒细胞胞质因子1,一种NADPH氧化酶复合物的组成成分)的自然多态性调节关节炎的严重程度。Ncf1与疾病相关的等位基因具有降低的氧化爆发反应,并促进致关节炎T细胞的激活。已证明用激活NADPH氧化酶复合物的物质进行药物治疗可改善关节炎。因此,Ncf1与一种导致严重破坏性关节炎的新自身免疫机制相关,这种机制与人类类风湿关节炎显著相似。