Sergeeva Marina, Rech Jürgen, Schett Georg, Hess Andreas
Institut for Experimental Pharmacology, Friedrich Alexander University Erlangen-Nürnberg, Fahrstrasse 17, 91054, Erlangen, Germany.
Department of Internal Medicine III, Friedrich Alexander University Erlangen-Nürnberg, Ulmenweg 18, 91054, Erlangen, Germany.
Arthritis Res Ther. 2015 Oct 19;17:268. doi: 10.1186/s13075-015-0783-2.
Chronic peripheral inflammation in diseases such as rheumatoid arthritis leads to alterations in central pain processing and consequently to mood disorders resulting from sensitization within the central nervous system and enhanced vulnerability of the medial pain pathway. Proinflammatory cytokines such as tumor necrosis factor (TNF) alpha play an important role herein, and therapies targeting their signaling (i.e., anti-TNF therapies) have been proven to achieve good results. However, the phenomenon of rapid improvement in the patients' subjective feeling after the start of TNFα neutralization remained confusing, because it was observed long before any detectable signs of inflammation decline. Functional magnetic resonance imaging (fMRI), enabling visualization of brain activity upon peripheral immune stimulation with anti-TNF, has helped to clarify this discrepancy. Moreover, fMRI appeared to work as a reliable tool for predicting prospective success of anti-TNF therapy, which is valuable considering the side effects of the drugs and the high therapy costs. This review, which is mainly guided by neuroimaging studies of the brain, summarizes the state-of-the-art knowledge about communication between the immune system and the brain and its impact on subjective well-being, addresses in more detail the outcome of the abovementioned anti-TNF fMRI studies (rapid response to TNFα blockade within the brain pain matrix and differences in brain activation patterns between prospective therapy responders and nonresponders), and discusses possible mechanisms for the latter phenomena and the predictive power of fMRI.
类风湿关节炎等疾病中的慢性外周炎症会导致中枢性疼痛处理发生改变,进而导致情绪障碍,这是由中枢神经系统内的敏化作用以及内侧疼痛通路的易损性增强所致。促炎细胞因子,如肿瘤坏死因子(TNF)α,在此过程中发挥着重要作用,针对其信号传导的疗法(即抗TNF疗法)已被证明能取得良好效果。然而,在开始TNFα中和治疗后,患者主观感觉迅速改善的现象仍令人困惑,因为这一现象早在任何可检测到的炎症消退迹象出现之前就已被观察到。功能磁共振成像(fMRI)能够在外周免疫刺激抗TNF的情况下可视化大脑活动,这有助于澄清这一差异。此外,fMRI似乎是预测抗TNF治疗预期成功的可靠工具,考虑到药物的副作用和高昂的治疗成本,这一点很有价值。本综述主要以大脑的神经影像学研究为指导,总结了关于免疫系统与大脑之间的通信及其对主观幸福感影响的最新知识,更详细地阐述了上述抗TNF fMRI研究的结果(大脑疼痛矩阵内对TNFα阻断的快速反应以及预期治疗反应者和无反应者之间大脑激活模式的差异),并讨论了后一种现象的可能机制以及fMRI的预测能力。