Tanaka Yoshiya
The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health.
Nihon Rinsho. 2009 Mar;67(3):619-25.
Rheumatoid arthritis (RA) is a chronic, systemic inflammatory disease that causes significant morbidity and mortality. RA patients should be started with DMARD represented by methotrexate (MTX) as early as possible. However, even use of MTX often fails to control disease activity and to prevent structural damage and, thereby, more effective treatment strategies are needed. Since TNF-alpha and IL-6 play a pivotal role in the pathological processes of RA, biologics targeting these cytokines with MTX, have revolutionized the treatment of RA, producing significant improvement in clinical, radiographic and functional outcomes not seen previously. However, even with these drugs the frequency and degree of responses are restricted. Therefore, new agents targeting cell surface molecules which are involved in cellular interaction and/or signaling on immune cells have been emerging, in order to increase response rates and to achieve high frequencies of remission or even cure. Two biologics abatacept, a CTLA4-Ig fusion protein, and rituximab, an anti-CD20 antibody, were launched in US and EU for the treatment of RA and many biologics are under the clinical trials from the similar concept. Thus, certain biologics have brought about paradigm shift in the treatment of rheumatic diseases, but an economical issue remains unsolved. In order to overcome the concern, low molecular weight chemical products have been rethought. Not a few agents targeting intracellular activation signaling in immune cells such as Jak and Syk are under clinical examinations and some of them appear to show wonderful results, which are comparable to biologics in the context of the treatment of rheumatic diseases. The prospects are here.
类风湿关节炎(RA)是一种慢性全身性炎症性疾病,可导致严重的发病率和死亡率。类风湿关节炎患者应尽早开始使用以甲氨蝶呤(MTX)为代表的改善病情抗风湿药(DMARD)。然而,即使使用甲氨蝶呤,也常常无法控制疾病活动和预防结构损伤,因此需要更有效的治疗策略。由于肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)在类风湿关节炎的病理过程中起关键作用,与甲氨蝶呤联合使用的靶向这些细胞因子的生物制剂彻底改变了类风湿关节炎的治疗方式,在临床、影像学和功能结局方面产生了前所未有的显著改善。然而,即使使用这些药物,反应的频率和程度仍然有限。因此,为了提高反应率并实现高缓解率甚至治愈,靶向参与免疫细胞细胞间相互作用和/或信号传导的细胞表面分子的新型药物不断涌现。两种生物制剂阿巴西普(一种CTLA4-Ig融合蛋白)和利妥昔单抗(一种抗CD20抗体)已在美国和欧盟获批用于治疗类风湿关节炎,许多基于类似概念的生物制剂正在进行临床试验。因此,某些生物制剂已经在风湿病治疗中带来了范式转变,但经济问题仍未解决。为了克服这一担忧,人们重新审视了低分子量化学产品。不少靶向免疫细胞内激活信号(如Jak和Syk)的药物正在进行临床研究,其中一些似乎显示出了出色的效果,在风湿病治疗方面可与生物制剂相媲美。前景就在这里。