Holmdahl R
Medical Inflammation Research, I11 BMC, Lund University, 22184 Lund, Sweden.
Ernst Schering Found Symp Proc. 2006(4):1-15. doi: 10.1007/2789_2007_036.
Inflammation is a physiological response that may go uncontrolled and thereby develop in a chronic way. This seems to happen in many common diseases of autoimmune, degenerative, or allergic character. Rheumatoid arthritis (RA) is by definition a chronic disease with an autoimmune inflammatory attack on diarthrodial cartilaginous joints. The development of new treatment neutralizing cytokines involved in the inflammatory attack has given relief and gives the promise of more effective treatment of already established disease. It is now time to set our eyes on a new vision to develop preventive and curative treatment based on knowledge of the unique and causative pathogenic mechanisms. To do this we believe it is important to identify the natural-selected polymorphisms that are associated with disease. These have proven to be extremely difficult to identify in complex diseases such as RA, but using animal models, this work is closer to reality. Animal models have recently been developed mimicking various aspects of the human disease. We will present an example in which a genetic polymorphism associated with the development of arthritis has been identified. On the basis of this finding, a new pathway involving control of immune tolerance by reactive oxidative species has been identified and a new class of antiinflammatory agents activating the induced oxidative burst protein complex is suggested.
炎症是一种生理反应,可能会失去控制,进而发展为慢性炎症。这似乎在许多自身免疫性、退行性或过敏性的常见疾病中都会发生。根据定义,类风湿性关节炎(RA)是一种慢性病,其对滑膜关节进行自身免疫性炎症攻击。中和参与炎症攻击的细胞因子的新疗法的出现带来了缓解效果,并有望更有效地治疗已确诊的疾病。现在是时候着眼于新的愿景,基于对独特的致病机制的了解来开发预防和治疗方法了。为此,我们认为识别与疾病相关的自然选择多态性很重要。在类风湿性关节炎等复杂疾病中,事实证明识别这些多态性极其困难,但利用动物模型,这项工作已更接近现实。最近已经开发出模仿人类疾病各个方面的动物模型。我们将展示一个例子,其中已识别出与关节炎发展相关的基因多态性。基于这一发现,已确定了一条涉及活性氧化物质控制免疫耐受的新途径,并提出了一类激活诱导性氧化爆发蛋白复合物的新型抗炎剂。