Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, 5200 Eastern Avenue, Mason F. Lord Building, Center Tower, Suite 4100, Room 412, Baltimore, MD 21224, USA.
Nat Rev Rheumatol. 2010 Jan;6(1):40-9. doi: 10.1038/nrrheum.2009.237.
A significant body of data implicates the type I interferon (IFN) pathway in the pathogenesis of autoimmune rheumatic diseases. In these disorders, a self-reinforcing cycle of IFN production can contribute to immunopathology through multiple mechanisms. Type I IFN cytokines are pleiotropic in their effects, mediating antiviral and antitumor activities, and possess numerous immunomodulatory functions for both the innate and adaptive immune responses. A key principle of the type I IFN system is rapid induction and amplification of the signaling pathway, which generates a feed-forward loop of IFN production, ensuring that a vigorous antiviral immune response is mounted. Although such feed-forward pathways are highly adaptive when it comes to rapid and effective virus eradication, this amplification can be maladaptive in immune responses directed against host tissues. Such feed-forward loops, however, create special opportunities for therapy.
大量数据表明,I 型干扰素(IFN)途径在自身免疫性风湿病的发病机制中起作用。在这些疾病中,IFN 产生的自我强化循环可通过多种机制导致免疫病理学。I 型 IFN 细胞因子在其作用上具有多效性,介导抗病毒和抗肿瘤活性,并对先天和适应性免疫反应具有多种免疫调节功能。I 型 IFN 系统的一个关键原则是信号通路的快速诱导和放大,这产生了 IFN 产生的正反馈环,确保了强大的抗病毒免疫反应的产生。尽管在快速有效清除病毒方面,这种正反馈途径具有高度适应性,但在针对宿主组织的免疫反应中,这种放大可能是不合适的。然而,这种正反馈环为治疗创造了特殊的机会。